SIALIDASE-PD-L1-ANTIBODY FUSION PROTEINS AND METHODS OF USE

THEREOF

CROSS REFERENCE TO RELATED APPLICATIONS

[0001] This application claims the benefit of, and priority to, U.S. Provisional Patent

Application serial number 62/870,354, filed July 3, 2019, and U.S. Provisional Patent

Application serial number 62/956,957, filed January 3, 2020, the entire disclosure of each of which is hereby incorporated by reference in its entirety.

FIELD OF THE INVENTION

[0002] The invention relates generally to recombinant sialidase fusion proteins and antibody conjugates, and their use in the treatment of cancer.

BACKGROUND

[0003] A growing body of evidence supports roles for glycans, and sialoglycans in particular, at various pathophysiological steps of tumor progression. Glycans regulate tumor proliferation, invasion, hematogenous metastasis and angiogenesis (Fuster et al. (2005) NAT. REV. CANCER 5(7): 526-42). The sialylation of cell surface glycoconjugates is frequently altered in cancers, resulting in the expression of sialylated tumor-associated carbohydrate antigens. The expression of sialylated glycans by tumor cells is often associated with increased aggressiveness and metastatic potential of a tumor.

[0004] It has recently become apparent that Siglecs (sialic acid-binding immunoglobulin-like lectins), a family of sialic acid binding lectins, play a role in cancer immune suppression by binding to hypersialylated cancer cells and mediating the suppression of signals from activating NK cell receptors, thereby inhibiting NK cell-mediated killing of tumor cells (Jandus et al. (2014) J. CLIN. INVEST. 124: 1810-1820; Laubli et al. (2014) PROC. NATL. ACAD. Sci. USA l l l : 14211-14216; Hudak et al. (2014) NAT. CHEM. BIOL. 10: 69-75). Likewise, enzymatic removal of sialic acids by treatment with sialidase can enhance NK cell-mediated killing of tumor cells (Jandus, supra ; Hudak, supra; Xiao et al. (2016) PROC. NATL. ACAD. SCI. USA 113(37): 10304- 9)·

[0005] Programmed death-ligand 1 (PD-L1) also known as cluster of differentiation 274 (CD274) or B7 homolog 1 (B7-H1) is a protein that in humans is encoded by the CD274 gene. Upregulation of PD-L1 may allow certain cancers to evade the host immune system. An analysis of 196 tumor specimens from patients with renal cell carcinoma found that high tumor expression of PD-L1 was associated with increased tumor aggressiveness and a 4.5-fold increased risk of death. Many PD-L1 antibodies are in development as immuno-oncology therapies and are showing good results in clinical trials including NSCLC and melanoma. PD-L1 expression is detected in most human cancers, including bladder, breast, cervical, esophageal, gastric, kidney, lung, ovary and pancreatic cancer. High expression of PD-L1 is associated with reduced numbers of tumor infiltrating lymphocytes and poor prognosis. Anti-PD-Ll antibodies include atezolizumab, approved for use in, for example, urothelial carcinomas, non-small cell lung cancers (NSCLC), triple-negative breast cancers, and small cell lung cancers, durvalumab, approved for use in, for example, urothelial carcinomas, and NSCLCs, and avelumab, approved for use in Merkel cell carcinomas, urothelial carcinomas, and renal cell carcinomas.

[0006] Cancer immunotherapy with immune checkpoint inhibitors, including antibodies blocking the PD-1/PD-L1 pathway, has improved the outcome of many cancer patients.

However, despite advances that have been made to date, many patients do not respond to currently available immune checkpoint inhibitors. Accordingly, there is still a need for effective interventions that overcome the immune suppressive tumor microenvironment and for treating cancers associated with hypersialylated cancer cells.

SUMMARY OF THE INVENTION

[0007] The invention is based, in part, upon the discovery that it is possible to produce fusion proteins containing a sialidase enzyme and an anti-PD-Ll immunoglobulin antigen-binding and/or antibody conjugates including a sialidase enzyme and an anti-PD-Ll antibody or a portion thereof. The fusion proteins and/or antibody conjugates have suitable substrate specificities and activities to be useful in removing sialic acid and/or sialic acid containing molecules from the surface of cancer cells, e.g., PD-L1 -expressing cancer cells, and/or removing sialic acid and/or sialic acid containing molecules from the tumor microenvironment, and/or reducing the concentration of sialic acid and/or sialic acid containing molecules in the tumor microenvironment.

[0008] Accordingly, in one aspect, the invention provides a fusion protein comprising (or consisting essentially of): (a) sialidase enzyme; and (b) an anti-PD-Ll immunoglobulin antigen binding domain.

[0009] In certain embodiments, the sialidase is a human sialidase, e.g, a recombinant mutant human sialidase. In certain embodiments, the sialidase comprises: (a) a substitution of a proline residue at a position corresponding to position 5 of wild-type human Neu2 (P5); (b) a substitution of a lysine residue at a position corresponding to position 9 of wild-type human Neu2 (K9); (c) a substitution of a lysine residue at a position corresponding to position 44 of wild-type human Neu2 (K44); (d) a substitution of a lysine residue at a position corresponding to position 45 of wild-type human Neu2 (K45); (e) a substitution of a leucine residue at a position corresponding to position 54 of wild-type human Neu2 (L54); (f) a substitution of a proline residue at a position corresponding to position 62 of wild-type human Neu2 (P62); (g) a substitution of a glutamine residue at a position corresponding to position 69 of wild-type human Neu2 (Q69); (h) a substitution of an arginine residue at a position corresponding to position 78 of wild-type human Neu2 (R78); (i) a substitution of an aspartic acid residue at a position corresponding to position 80 of wild-type human Neu2 (D80); (j) a substitution of an alanine residue at a position corresponding to position 93 of wild-type human Neu2 (A93); (k) a substitution of a glycine residue at a position corresponding to position 107 of wild-type human Neu2 (G107); (1) a substitution of a glutamine residue at a position corresponding to position 108 of wild-type human Neu2 (Q108); (m) a substitution of a glutamine residue at a position corresponding to position 112 of wild-type human Neu2 (Q112); (n) a substitution of a cysteine residue at a position corresponding to position 125 of wild-type human Neu2 (Cl 25); (o) a substitution of a glutamine residue at a position corresponding to position 126 of wild-type human Neu2 (Q126); (p) a substitution of an alanine residue at a position corresponding to position 150 of wild-type human Neu2 (A150); (q) a substitution of a cysteine residue at a position corresponding to position 164 of wild-type human Neu2 (Cl 64); (r) a substitution of an arginine residue at a position corresponding to position 170 of wild-type human Neu2 (R170);

(s) a substitution of an alanine residue at a position corresponding to position 171 of wild-type human Neu2 (A171); (t) a substitution of a glutamine residue at a position corresponding to position 188 of wild-type human Neu2 (Q188); (u) a substitution of an arginine residue at a position corresponding to position 189 of wild-type human Neu2 (R189); (v) a substitution of an alanine residue at a position corresponding to position 213 of wild-type human Neu2 (A213);

(w) a substitution of a leucine residue at a position corresponding to position 217 of wild-type human Neu2 (L217); (x) a substitution of a glutamic acid residue at a position corresponding to position 225 of wild-type human Neu2 (E225); (y) a substitution of a histidine residue at a position corresponding to position 239 of wild-type human Neu2 (H239); (z) a substitution of a leucine residue at a position corresponding to position 240 of wild-type human Neu2 (L240);

(aa) a substitution of an arginine residue at a position corresponding to position 241 of wild-type human Neu2 (R241); (bb) a substitution of an alanine residue at a position corresponding to position 242 of wild-type human Neu2 (A242); (cc) a substitution of a valine residue at a position corresponding to position 244 of wild-type human Neu2 (V244); (dd) a substitution of a threonine residue at a position corresponding to position 249 of wild-type human Neu2 (T249); (ee) a substitution of an aspartic acid residue at a position corresponding to position 251 of wild- type human Neu2 (D251); (ff) a substitution of a glutamic acid residue at a position

corresponding to position 257 of wild-type human Neu2 (E257); (gg) a substitution of a serine residue at a position corresponding to position 258 of wild-type human Neu2 (S258); (hh) a substitution of a leucine residue at a position corresponding to position 260 of wild-type human Neu2 (L260); (ii) a substitution of a valine residue at a position corresponding to position 265 of wild-type human Neu2 (V265); (jj) a substitution of a glutamine residue at a position

corresponding to position 270 of wild-type human Neu2 (Q270); (kk) a substitution of a tryptophan residue at a position corresponding to position 292 of wild-type human Neu2

(W292); (11) a substitution of a serine residue at a position corresponding to position 301 of wild- type human Neu2 (S301); (mm) a substitution of a tryptophan residue at a position

corresponding to position 302 of wild-type human Neu2 (W302); (nn) a substitution of a valine residue at a position corresponding to position 363 of wild-type human Neu2 (V363); or (oo) a substitution of a leucine residue at a position corresponding to position 365 of wild-type human Neu2 (L365); or a combination of any of the foregoing substitutions. For example, the sialidase may comprise a substitution of K9, P62, A93, Q216, A242, Q270, S301, W302, V363, or L365, or a combination of any of the foregoing substitutions.

[0010] In certain embodiments, in the sialidase: (a) the proline residue at a position

corresponding to position 5 of wild-type human Neu2 is substituted by histidine (P5H); (b) the lysine residue at a position corresponding to position 9 of wild-type human Neu2 is substituted by aspartic acid (K9D); (c) the lysine residue at a position corresponding to position 44 of wild- type human Neu2 is substituted by arginine (K44R) or glutamic acid (K44E); (d) the lysine residue at a position corresponding to position 45 of wild-type human Neu2 is substituted by alanine (K45 A), arginine (K45R), or glutamic acid (K45E); (e) the leucine residue at a position corresponding to position 54 of wild-type human Neu2 is substituted by methionine (L54M); (f) the proline residue at a position corresponding to position 62 of wild-type human Neu2 is substituted by asparagine (P62N), aspartic acid (P62D), histidine (P62H), glutamic acid (P62E), glycine (P62G), serine (P62S), or threonine (P62T); (g) the glutamine residue at a position corresponding to position 69 of wild-type human Neu2 is substituted by histidine (Q69H); (h) the arginine residue at a position corresponding to position 78 of wild-type human Neu2 is substituted by lysine (R78K); (i) the aspartic acid residue at a position corresponding to position 80 of wild-type human Neu2 is substituted by proline (D80P); (j) the alanine residue at a position corresponding to position 93 of wild-type human Neu2 is substituted by glutamic acid (A93E) or lysine (A93K); (k) the glycine residue at a position corresponding to position 107 of wild-type human Neu2 is substituted by aspartic acid (G107D); (1) the glutamine residue at a position corresponding to position 108 of wild-type human Neu2 is substituted by histidine (Q108H); (m) the glutamine residue at a position corresponding to position 112 of wild-type human Neu2 is substituted by arginine (Q112R) or lysine (Q112K); (n) the cysteine residue at a position corresponding to position 125 of wild-type human Neu2 is substituted by leucine (C125L); (o) the glutamine residue at a position corresponding to position 126 of wild-type human Neu2 is substituted by leucine (Q126L), glutamic acid (Q126E), phenylalanine (Q126F), histidine (Q126H), isoleucine (Q126I), or tyrosine (Q126Y); (p) the alanine residue at a position corresponding to position 150 of wild-type human Neu2 is substituted by valine (A150V); (q) the cysteine residue at a position corresponding to position 164 of wild-type human Neu2 is substituted by glycine (C164G); (r) the arginine residue at a position corresponding to position 170 of wild-type human Neu2 is substituted by proline (R170P); (s) the alanine residue at a position corresponding to position 171 of wild-type human Neu2 is substituted by glycine (A171G); (t) the glutamine residue at a position corresponding to position 188 of wild-type human Neu2 is substituted by proline (Q188P); (u) the arginine residue at a position

corresponding to position 189 of wild-type human Neu2 is substituted by proline (R189P); (v) the alanine residue at a position corresponding to position 213 of wild-type human Neu2 is substituted by cysteine (A213C), asparagine (A213N), serine (A213S), or threonine (A213T); (w) the leucine residue at a position corresponding to position 217 of wild-type human Neu2 is substituted by alanine (L217A) or valine (L217V); (x) the threonine residue at a position corresponding to position 249 of wild-type human Neu2 is substituted by alanine (T249A); (y) the aspartic acid residue at a position corresponding to position 251 of wild-type human Neu2 is substituted by glycine (D251G); (z) the glutamic acid residue at a position corresponding to position 225 of wild-type human Neu2 is substituted by proline (E225P); (aa) the histidine residue at a position corresponding to position 239 of wild-type human Neu2 is substituted by proline (H239P); (bb) the leucine residue at a position corresponding to position 240 of wild- type human Neu2 is substituted by aspartic acid (L240D), asparagine (L240N), or tyrosine (L240Y); (cc) the arginine residue at a position corresponding to position 241 of wild-type human Neu2 is substituted by alanine (R241 A), aspartic acid (R241D), leucine (R241L), glutamine (R241Q). or tyrosine (R241Y); (dd) the alanine residue at a position corresponding to position 242 of wild-type human Neu2 is substituted by cysteine (A242C), phenylalanine (A242F), glycine (A242G), histidine (A242H), isoleucine (A242I), lysine (A242K), leucine (A242L), methionine (A242M), asparagine (A242N), glutamine (A242Q), arginine (A242R), serine (A242S), valine (A242V), tryptophan (A242W), or tyrosine (A242Y); (ee) the valine residue at a position corresponding to position 244 of wild-type human Neu2 is substituted by isoleucine (V244I), lysine (V244K), or proline (V244P); (ff) the glutamic acid residue at a position corresponding to position 257 of wild-type human Neu2 is substituted by proline (E257P); (gg) the serine residue at a position corresponding to position 258 is substituted by cysteine (S258C); (hh) the leucine residue at a position corresponding to position 260 of wild- type human Neu2 is substituted by aspartic acid (L260D), phenylalanine (L260F), glutamine (L260Q), or threonine (L260T); (ii) the valine residue at a position corresponding to position 265 of wild-type human Neu2 is substituted by phenylalanine (V265F); (jj) the glutamine residue at a position corresponding to position 270 of wild-type human Neu2 is substituted by alanine (Q270A), histidine (Q270H), phenylalanine (Q270F), proline (Q270P), serine (Q270S), or threonine (Q270T); (kk) the tryptophan residue at a position corresponding to position 292 of wild-type human Neu2 is substituted by arginine (W292R); (11) the serine residue at a position corresponding to position 301 of wild-type human Neu2 is substituted by alanine (S301 A), aspartic acid (S301D), glutamic acid (S301E), phenylalanine (S301F), histidine (S301H), lysine (S301K), leucine (S301L), methionine (S301M), asparagine (S301N), proline (S301P), glutamine (S301Q), arginine (S301R), threonine (S301T), valine (S301V), tryptophan (S301W), or tyrosine (S301 Y); (mm) the tryptophan residue at a position corresponding to position 302 of wild-type human Neu2 is substituted by alanine (W302A), aspartic acid (W302D), phenylalanine (W302F), glycine (W302G), histidine (W302H), isoleucine (W302I), lysine (W302K), leucine (W302L), methionine (W302M), asparagine (W302N), proline (W302P), glutamine (W302Q), arginine (W302R), serine (W302S), threonine (W302T), valine (W302V), or tyrosine (W302Y); (nn) the valine residue at a position corresponding to position 363 of wild-type human Neu2 is substituted by arginine (V363R); or (oo) the leucine residue at a position corresponding to position 365 of wild-type human Neu2 is substituted by glutamine (L365Q), histidine (L365H), isoleucine (L365I), lysine (L365K) or serine (L365S); or the sialidase comprises a combination of any of the foregoing substitutions. For example, the sialidase may comprise a substitution selected from K9D, P62G, P62N, P62S, P62T, A93E, Q126Y, A242F, A242W, A242Y, Q270A, Q270T, S301A, S301R, W302K, W302R, V363R, and L365I, or a combination of any of the foregoing substitutions.

[0011] In certain embodiments, the sialidase comprises: (a) a substitution or deletion of a methionine residue at a position corresponding to position 1 of wild-type human Neu2 (Ml); (b) a substitution of a valine residue at a position corresponding to position 6 of wild-type human Neu2 (V6); (c) a substitution of an isoleucine residue at a position corresponding to position 187 of wild-type human Neu2 (1187); or (d) a substitution of a cysteine residue at a position corresponding to position 332 of wild-type human Neu2 (C332); or a combination of any of the foregoing substitutions.

[0012] In certain embodiments, in the sialidase: (a) the methionine residue at a position corresponding to position 1 of wild-type human Neu2 is deleted (DM1), is substituted by alanine (MIA), or is substituted by aspartic acid (MID); (b) the valine residue at a position

corresponding to position 6 of wild-type human Neu2 is substituted by tyrosine (V6Y); (c) the isoleucine residue at a position corresponding to position 187 of wild-type human Neu2 is substituted by lysine (I187K); or (d) the cysteine residue at a position corresponding to position 332 of wild-type human Neu2 is substituted by alanine (C332A); or the sialidase comprises a combination of any of the foregoing substitutions.

[0013] In certain embodiments, the sialidase comprises: (a) the MID, V6Y, P62G, A93E,

I187K, and C332A substitutions; (b) the MID, V6Y, K9D, A93E, I187K, C332A, V363R, and L365I substitutions; (c) the MID, V6Y, P62N, I187K, and C332A substitutions; (d) the MID, V6Y, I187K, Q270A, S301R, W302K, and C332A substitutions; (e) the MID, V6Y, P62S, I187K, Q270A, S301R, W302K, and C332A substitutions; (f) the MID, V6Y, P62T, I187K, Q270A, S301R, W302K, and C332A substitutions; (g) the MID, V6Y, P62N, I187K, Q270A, S301R, W302K, and C332A substitutions; (h) the MID, V6Y, P62G, A93E, I187K, S301A, W302R, and C332A substitutions; (i) the MID, V6Y, P62G, A93E, Q126Y, I187K, Q270T, and C332A substitutions; G) the MID, V6Y, P62G, A93E, Q126Y, I187K, and C332A substitutions; or (k) the MID, V6Y, P62G, A93E, Q126Y, I187K, A242F, Q270T, and C332A substitutions.

[0014] In certain embodiments, the sialidase is selected from Neul, Neu2, Neu3, and Neu4, e.g, the sialidase is Neu2.

[0015] In certain embodiments, the sialidase has a different substrate specificity than the corresponding wild-type sialidase. For example, in certain embodiments the sialidase can cleave a2,3, a2,6, and/or a2,8 linkages. In certain embodiments the sialidase can cleave a2,3 and a2,8 linkages.

[0016] In certain embodiments, the sialidase comprises any one of SEQ ID NOs: 48-62, 94, 97, 100, or 126, or an amino acid sequence that has at least 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to any one of SEQ ID NOs: 48-62, 94, 97, 100, or 126.

[0017] In certain embodiments, the sialidase comprises mutation or combination of mutations set forth in any one of Tables 5-12 or 14-27. In certain embodiments, the sialidase comprises a mutation or combination of mutations set forth in any one of Tables 1-4. [0018] In certain embodiments, the fusion protein further comprises an immunoglobulin Fc domain. In certain embodiments, the immunoglobulin Fc domain is derived from a human IgGl, IgG2, IgG3, IgG4, IgAl, IgA2, IgD, IgE, or IgM Fc domain, e.g., the immunoglobulin Fc domain is derived from a human IgGl, IgG2, IgG3, or IgG4 Fc domain, e.g, the

immunoglobulin Fc domain is derived from a human IgGl Fc domain.

[0019] In certain embodiments, the anti-PD-Ll immunoglobulin antigen-binding domain is associated (for example, covalently or non-covalently associated) with a second anti-PD-Ll immunoglobulin antigen-binding domain to produce an anti-PD-Ll antigen-binding site.

[0020] In certain embodiments, the anti-PD-Ll immunoglobulin antigen-binding domain is derived from an antibody selected from avelumab, atezolizumab, durvalumab, MED 14736, CSIOOI, KL-A167, CK-301, TQB2450, KN035, SHR-1316, STI-A1014, BGB-A333,

MSB2311, HLX-20 and BMS-936559, e.g., the anti-PD-Ll immunoglobulin antigen-binding domain is derived from avelumab.

[0021] In certain embodiments, the sialidase and the immunoglobulin Fc domain and/or the anti- PD-Ll immunoglobulin antigen-binding domain are linked by a peptide bond or an amino acid linker.

[0022] In certain embodiments, the fusion protein comprises any one of SEQ ID NOs: 65-75, 78, 81-89, 95, 96, 98, 99, 101, 102, 104, 106, 108, 110, 112, 114, 122-124, 127, or 128.

[0023] In another aspect, the invention provides an antibody conjugate comprising any of the foregoing fusion proteins. In certain embodiments, the antibody conjugate comprises a single sialidase. In other embodiments, the antibody conjugate comprises two sialidases, which can be the same or different. In certain embodiments the antibody conjugate comprises two identical sialidases. In certain embodiments, the antibody conjugate comprises a single anti-PD-Ll antigen-binding site. In other embodiments, the antibody conjugate comprises two anti-PD-Ll antigen-binding sites, which can be the same or different. In certain embodiments, the antibody conjugate comprises two identical anti-PD-Ll antigen-binding sites.

[0024] In certain embodiments, the antibody conjugate has a molecular weight from about 135 kDa to about 165 kDa, or the antibody conjugate has a molecular weight from about 215 kDa to about 245 kDa.

[0025] In certain embodiments, the antibody conjugate comprises: (a) a first polypeptide comprising an immunoglobulin light chain; (b) a second polypeptide comprising an

immunoglobulin heavy chain; and (c) a third polypeptide comprising an immunoglobulin Fc domain and a sialidase; wherein the first and second polypeptides are covalently linked together and the second and third polypeptides are covalently linked together, and wherein the first polypeptide and the second polypeptide together define an anti-PD-Ll antigen-binding site. The third polypeptide may, for example, comprise the sialidase and the immunoglobulin Fc domain in an N- to C-terminal orientation. The first polypeptide may, for example, comprise SEQ ID NO: 65, the second polypeptide may, for example, comprise any one of SEQ ID NOs: 66, 104, or 124, and/or the third polypeptide may, for example, comprise any one of SEQ ID NOs: 67-73, 78, 81-87, 95, 96, 98, 99, 101, 102, 106, 108, 112, 122, 123, 127, or 128.

[0026] In certain embodiments, the antibody conjugate comprises: (a) a first polypeptide comprising a first immunoglobulin light chain; (b) a second polypeptide comprising a first immunoglobulin heavy chain and a first sialidase; (c) a third polypeptide comprising a second immunoglobulin heavy chain and a second sialidase; and (d) a fourth polypeptide comprising a second immunoglobulin light chain; wherein the first and second polypeptides are covalently linked together, the third and fourth polypeptides are covalently linked together, and the second and third polypeptides are covalently linked together, and wherein the first polypeptide and the second polypeptide together define a first anti-PD-Ll antigen-binding site, and the third polypeptide and the fourth polypeptide together define a second anti-PD-Ll antigen-binding site. The second and third polypeptides may, for example, comprise the first and second

immunoglobulin heavy chain and the first and second sialidase, respectively, in an N- to C- terminal orientation.

[0027] In certain embodiments, the antibody conjugate comprises: (a) a first polypeptide comprising a first sialidase, a first immunoglobulin Fc domain, and a first single chain variable fragment (scFv); and (b) a second polypeptide comprising a second sialidase, a second immunoglobulin Fc domain, and an optional second single chain variable fragment (scFv);

wherein the first and second polypeptides are covalently linked together, and wherein the first scFv defines a first anti-PD-Ll antigen-binding site, and the second scFv, when present, defines a second anti-PD-Ll antigen-binding site. The first polypeptide may, for example comprise the first sialidase, the first immunoglobulin Fc domain, and the first scFv in an N- to C-terminal orientation. The second polypeptide may, for example, comprise the second sialidase, the second immunoglobulin Fc domain, and the optional second scFv in an N- to C-terminal orientation. The first polypeptide may, for example, comprise SEQ ID NO: 114, and/or the second polypeptide may, for example, comprise SEQ ID NO: 114. [0028] In certain embodiments, the antibody conjugate comprises: (a) a first polypeptide comprising an immunoglobulin light chain; (b) a second polypeptide comprising an

immunoglobulin heavy chain and a single chain variable fragment (scFv); and (c) a third polypeptide comprising an immunoglobulin Fc domain and a sialidase, wherein the first and second polypeptides are covalently linked together and the second and third polypeptides are covalently linked together, and wherein the immunoglobulin light chain and immunoglobulin heavy chain together define a first anti-PD-Ll antigen-binding site and the scFv defines a second anti-PD-Ll antigen-binding site. The second polypeptide may, for example comprise the immunoglobulin heavy chain and the scFv in an N- to C-terminal orientation. The third polypeptide may, for example, comprise the sialidase and the immunoglobulin Fc domain in an N- to C-terminal orientation. The first polypeptide may, for example, comprise SEQ ID NO: 65, the second polypeptide may, for example, comprise SEQ ID NO: 110, and/or the third polypeptide may, for example, comprise any one of SEQ ID NOs: 78 or 106.

[0029] In another aspect, the invention provides an isolated nucleic acid comprising a nucleotide sequence encoding any of the foregoing fusion proteins or at least a portion of any of the foregoing antibody conjugates. In another aspect, the invention provides an expression vector comprising any of the foregoing nucleic acids. In another aspect, the invention provides a host cell comprising any of the foregoing expression vectors.

[0030] In another aspect, the invention provides a pharmaceutical composition comprising any of the foregoing fusion proteins or any of the foregoing antibody conjugates.

[0031] In another aspect, the invention provides a method of treating cancer in a subject in need thereof. The method comprises administering to the subject an effective amount of any of the foregoing fusion proteins, any of the foregoing antibody conjugates, or any of the foregoing pharmaceutical compositions.

[0032] In certain embodiments, the cancer is selected from non-small cell lung cancer (NSCLC), melanoma, bladder, breast, cervical, esophageal, gastric, kidney, lung, ovary, metastatic Merkel cell carcinoma (MCC), metastatic urothelial carcinoma (UC), and pancreatic cancer. For example, in certain embodiments, the cancer is NSCLC or melanoma.

[0033] These and other aspects and features of the invention are described in the following detailed description and claims. DESCRIPTION OF THE DRAWINGS

[0034] The invention can be more completely understood with reference to the following drawings.

[0035] FIGURE 1 depicts an SDS-PAGE gel showing recombinant human Neul, Neu2, Neu3, and Salmonella typhimurium (St-sialidase) under non-reducing and reducing conditions.

Monomer and dimer species are indicated.

[0036] FIGURE 2 is a bar graph showing the enzymatic activity of recombinant human Neul, Neu2, and Neu3.

[0037] FIGURE 3 is a line graph showing enzymatic activity as a function of substrate concentration for recombinant human Neu2 and Neu3 at the indicated pH.

[0038] FIGURE 4 depicts a schematic representation of an exemplary sialic acid biotinylated probe that can be used in phage display or yeast display screening for Neu2 variants.

[0039] FIGURE 5 depicts an exemplary protocol that facilitates phage display screening of Neu2 variants.

[0040] FIGURE 6 depicts an exemplary protocol that facilitates yeast display screening of Neu2 variants.

[0041] FIGURE 7A depicts an SDS-PAGE gel showing recombinant Neu2-Fc (wildtype) and Neu2-M106-Fc under non-reducing and reducing conditions. FIGURE 7B is an SEC-HPLC trace of Neu2-Fc (wildtype) and Neu2-M106-Fc. The monomer species has a retention time of 21 minutes.

[0042] FIGURE 8 is a line graph depicting the enzymatic activity of Neu2 variant M106.

[0043] FIGURE 9A depicts an SDS-PAGE gel showing Neu2-M173-Fc under non-reducing and reducing conditions. FIGURE 9B is an SEC-HPLC trace of Neu2-M173-Fc. The monomer species has a retention time of 6.367 minutes. The monomer species has a purity of

approximately 90% after purification by Protein A and CHT chromatography.

[0044] FIGURE 10 depicts the enzyme activity of Neu2-M173-Fc, using 4-MU-Neu5Ac as the substrate, and fixing enzyme concentration to 2 pg/well.

[0045] FIGURE 11A depicts an SDS-PAGE gel showing Neu2-M106 under non-reducing (NR) and reducing (R) conditions. FIGURE 11B depicts a schematic representation of the Neu2 structure with the position of the R243 cleavage site indicated. [0046] FIGURE 12 depicts a reducing SDS-PAGE gel showing Neu2-M106 produced by a large or small scale expression with (+) or without (-) trypsin treatment.

[0047] FIGURE 13 depicts an SDS-PAGE gel showing Neu2-M106 following incubation with trypsin and one of the protease inhibitors iron citrate (Fe Cit), aprotinin, AEBSF, leupeptin, or E- 64 at the indicated concentrations.

[0048] FIGURE 14 is a table depicting different mutations and combinations of mutations surrounding the trypsin cleavage site in Neu2.

[0049] FIGURE 15A depicts a reducing SDS-PAGE analysis of Neu2 variants with the indicated mutation at position A242 with or without trypsin treatment. Trypsin digestion was for 5 minutes at 4 °C using a 5,000% dilution of trypsin. The digestion was quenched by addition of SDS, and 2 pg of protein was loaded on the gel. FIGURE 15B depicts the enzymatic activity of Neu2 variants with the indicated mutation at position A242. FIGURE 15C is an SEC-HPLC trace of Neu2 variants with the indicated mutation at position A242. Neu2-M106 (the mutational background in which the mutations at position A242 were tested) is shown as a control.

[0050] FIGURE 16 depicts a reducing SDS-PAGE analysis of the indicated Neu2 variants with or without trypsin treatment. Neu2-M106 is shown as a control. For example, Neu2-M255 was shown to have a greater than 10 fold improved trypsin resistance relative to Neu2-M106.

[0051] FIGURES 17A-17I depict schematic representations of certain antibody conjugate constructs containing a sialidase enzyme, e.g ., a human sialidase enzyme, and an anti-PD-Ll antigen binding site. For each antibody conjugate construct that contains more than one (e.g, two) sialidase, each sialidase may be the same or different. For each antibody conjugate construct that contains more than one (e.g, two) anti-PD-Ll antigen binding site, each anti-PD- Ll antigen binding site may be the same or different. For each antibody conjugate construct that contains an Fc domain, it is understood that the Fc domain can be a wild type Fc domain or can be an engineered Fc domain. For example, the Fc domain may be engineered to contain either a “knob” mutation, e.g, T366Y, or a“hole” mutation, e.g, Y407T, or both, to promote

heterodimerization, or the Fc domain may be engineered to contain one or more modifications, e.g. , point mutations, to provide any other modified Fc domain functionality.

[0052] FIGURE 18 depicts schematic representations of certain antibody conjugate constructs containing a sialidase enzyme, e.g. , a human sialidase enzyme, and an antigen binding site. For each antibody conjugate construct that contains more than one (e.g, two) antigen binding site, each antigen binding site may be the same or different. For each antibody conjugate construct that contains an Fc domain, it is understood that the Fc domain can be a wild type Fc domain or can be an engineered Fc domain. For example, the Fc domain may be engineered to contain either a“knob” mutation, e.g., T366Y, or a“hole” mutation, e.g, Y407T, or both, to promote heterodimerization, or the Fc domain may be engineered to contain one or more modifications, e.g. , point mutations, to provide any other modified Fc domain functionality.

[0053] FIGURES 19A-19D are schematic representations of exemplary fusion protein conjugates referred to as a Raptor antibody sialidase conjugate (FIGURE 19A), a Janus antibody sialidase conjugate (FIGURE 19B), a Lobster antibody sialidase conjugate (FIGURE 19C), and a Bunk antibody sialidase conjugate (FIGURE 19D).

[0054] FIGURE 20 depicts an SDS-PAGE gel showing purified recombinant human Janus # 1 (“Janus”) under non-reducing and reducing conditions.

[0055] FIGURE 21 shows an SEC-HPLC trace of purified Janus #1, showing approximately 85% monomer purity.

[0056] FIGURE 22 is a line graph showing the enzyme activity of Janus #1 using 4-MU- Neu5Ac as the substrate and measured as the level of fluorescence (AU) generated.

Specifically, when Janus #1 is incubated with the fluorogenic substrate 4-MU-Neu5Ac, it cleaves the substrate, generating fluorescence which is indicative of the sialidase activity of the construct.

[0057] FIGURE 23A is an Octet binding graph showing the binding of avelumab to the PD-L1 antigen and FIGURE 23B is an octet binding graph showing the binding of Janus #1 (“Ave- Janus”) to the PD-L1 antigen. Kinetic binding experiments were carried out using ForteBio Octet. FIGURE 23C is a table showing equilibrium dissociation constant (KD), k _on , and k _diS for avelumab and Janus #1 (“Ave- Janus”).

[0058] FIGURE 24 depicts schematic representations of certain antibody conjugate constructs containing a sialidase enzyme and an anti-PD-Ll antigen binding site. Individual components of the constructs, including a Salmonella typhimurium sialidase (St-sia), a human Neu2 sialidase (Neu2), an immunoglobulin Fc domain including a T366Y knob mutation (Fc-knob), an immunoglobulin Fc domain including a Y407T hole mutation (Fc-hole), an anti-PD-Ll antigen binding fragment (Fab), an anti-PD-Ll single-chain variable fragment (scFv) and a histidine tag (his-tag) are indicated. Constructs that correspond to Janus #1, Janus #2, Janus #3, Janus #4, Bunk #1, Bunk #2 and Lobster #1, as described in Examples 5 and 6, are indicated. [0059] FIGURE 25 is a line graph depicting the enzymatic activity of Janus #1, Janus #2, Lobster #1, Bunk #1, Bunk #2, and Neu2-M106-Fc (“Ml 06 FC”).

[0060] FIGURE 26 depicts size exclusion chromatography (SEC) profiles of the indicated avelumab-based ASCs as well as the monomer purity of each.

[0061] FIGURE 27 is an Octet binding graph showing the binding of avelumab and the indicated avelumab-based ASCs to PD-L1 antigen.

[0062] FIGURE 28 is an Octet binding graph showing the binding of PD-L1 to the indicated avelumab-based ASCs.

[0063] FIGURE 29 is a schematic representation of a cell-based PD-1/PD-L1 blockade bioassay.

[0064] FIGURE 30 depicts the ability of the indicated avelumab-based ASCs to block the interaction of PD-L1 with PD-1 as measured using the assay depicted in FIGURE 29. Antibody blockade is indicated by an increase in luminescence. Relative light units (RLU) were calculated by subtracting background (substrate and media only) from assay wells. Fold induction was calculated by dividing RLU (induced minus background) by RLU (no antibody control minus background). The EC50 for each ASC and avelumab is shown based on curve fitting fold induction data as determined by Prism.

[0065] FIGURE 31 depicts the in vivo efficacy of the indicated avelumab-based ASCs at the indicated dose in a mouse A20 syngeneic subcutaneous tumor model. Tumor growth curves for each mouse are depicted. Observed partial responses (PR) and complete responses (CR) are also indicated.

[0066] FIGURE 32 depicts the in vivo efficacy of the indicated avelumab-based ASCs in a mouse A20 syngeneic subqutaneous tumor model. Tumor growth curves for each mouse are depicted. Triangles indicate dosing.

DETAILED DESCRIPTION

[0067] Various features and aspects of the invention are discussed in more detail below.

[0068] The invention relates to fusion proteins and/or antibody conjugates comprising a sialidase enzyme and an anti-PD-Ll antibody or portion thereof, e.g. , an immunoglobulin Fc domain and/or an antigen-binding domain. The sialidase enzyme portion of the fusion protein and/or antibody conjugate may comprise at least one mutation relative to a wild-type sialidase. The mutations, or combination of mutations, can improve the expression, activity or both the expression and activity of the sialidase to improve its use in cancer diagnosis and/or treatment.

[0069] The invention further relates to pharmaceutical compositions and methods of using fusion proteins and/or antibody conjugates to treat cancer.

I. Sialidase anti-PD-Ll Fusion Proteins

[0070] To promote the selective removal of sialic acids on hypersialylated cancer cells, e.g., PD- L1 expressing cancer cells, and/or in the tumor microenvironment, it may be helpful to target a sialidase as described herein to such a cell or to such a tumor microenvironment. Additionally, in order to promote the removal of sialic acid by a sialidase in a subject, it may be helpful to extend the plasma half-life of the sialidase in the subject. These can be achieved by including the sialidase in a fusion protein and/or antibody conjugate (e.g, a chemically conjugated conjugate).

[0071] Accordingly, the invention further provides fusion proteins comprising a sialidase enzyme, or a functional fragment thereof, and a portion or fragment of an anti-PD-Ll antibody, such as an immunoglobulin Fc domain (also referred to herein as an Fc domain), or an immunoglobulin antigen-binding domain (also referred to herein as an antigen-binding domain). In certain embodiments, the sialidase and anti-PD-Ll antibody or portion thereof (e.g, immunoglobulin Fc domain or antigen-binding domain) are linked by a peptide bond or an amino acid linker.

[0072] As used herein, unless otherwise indicated, the term“fusion protein” is understood to refer to a single polypeptide chain comprising amino acid sequences based upon two or more separate proteins or polypeptide chains, where the two amino acid sequences may be fused together directly or via an intervening linker sequence, e.g, via an intervening amino acid linker. A nucleotide sequence encoding such a fusion protein can, for example, be created using conventional recombinant DNA technologies.

[0073] In certain embodiments, a fusion protein comprises a tag, such as a Strep tag (e.g, a Strep II tag), a His tag (e.g, a lOx His tag), a myc tag, or a FLAG tag. The tag can be located on the C-terminus or the N-terminus of the fusion protein.

a. Sialidase Portion

[0074] As used herein, the term“sialidase” refers to any enzyme, or a functional fragment thereof, that cleaves a terminal sialic acid residue from a substrate, for example, a glycoprotein or a glycolipid. The term sialidase includes variants having one or more amino acid substitutions, deletions, or insertions relative to a wild-type sialidase sequence, and/or fusion proteins or conjugates including a sialidase. Sialidases are also called neuraminidases, and, unless indicated otherwise, the two terms are used interchangeably herein. As used herein, the term“functional fragment” of a sialidase refers to fragment of a full-length sialidase that retains, for example, at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or 100% of the enzymatic activity of the corresponding full-length, naturally occurring sialidase. Sialidase enzymatic activity may be assayed by any method known in the art, including, for example, by measuring the release of sialic acid from the fluorogenic substrate 4-methylumbelliferyl-N-acetylneuraminic acid (4MU- NeuAc). In certain embodiments, the functional fragment comprises at least 100, 150, 200, 250, 300, 310, 320, 330, 340, 350, 360, or 370 consecutive amino acids present in a full-length, naturally occurring sialidase.

[0075] In certain embodiments, a sialidase portion of a sialidase-anti-PD-Ll fusion protein is derived from a eukaryotic sialidase, e.g., a mammalian sialidase, e.g, a human or mouse sialidase.

[0076] Four sialidases are encoded in the human genome: Neul, Neu2, Neu3 and Neu4. Human Neul is a lysosomal neuraminidase enzyme which functions in a complex with beta- galactosidase and cathepsin A. The amino acid sequence of human Neul is depicted in SEQ ID NO: 7, and a nucleotide sequence encoding human Neul is depicted in SEQ ID NO: 23.

[0077] Human Neu2 is a cytosolic sialidase enzyme. The amino acid sequence of human Neu2 is depicted in SEQ ID NO: 1, and a nucleotide sequence encoding human Neu2 is depicted in SEQ ID NO: 24. Unless stated otherwise, as used herein, wild-type human Neu2 refers to human Neu2 having the amino acid sequence of SEQ ID NO: 1.

[0078] Human Neu3 is a plasma membrane sialidase with an activity specific for gangliosides. Human Neu3 has two isoforms: isoform 1 and isoform 2. The amino acid sequence of human Neu3, isoform 1 is depicted in SEQ ID NO: 8, and a nucleotide sequence encoding human Neu3, isoform 1 is depicted in SEQ ID NO: 25. The amino acid sequence of human Neu3, isoform 2 is depicted in SEQ ID NO: 9, and a nucleotide sequence encoding human Neu3, isoform 2 is depicted in SEQ ID NO: 34.

[0079] Human Neu4 has two isoforms: isoform l is a peripheral membrane protein and isoform 2 localizes to the lysosome lumen. The amino acid sequence of human Neu4, isoform 1 is depicted in SEQ ID NO: 10, and a nucleotide sequence encoding human Neu4, isoform 1 is depicted in SEQ ID NO: 26. The amino acid sequence of human Neu4, isoform 2 is depicted in SEQ ID NO: 11, and a nucleotide sequence encoding human Neu4, isoform 2 is depicted in SEQ ID NO: 35.

[0080] Four sialidases have also been found in the mouse genome and are referred to as Neul, Neu2, Neu3 and Neu4. The amino acid sequence of mouse Neul is depicted in SEQ ID NO: 38, and a nucleotide sequence encoding mouse Neul is depicted in SEQ ID NO: 42. The amino acid sequence of mouse Neu2 is depicted in SEQ ID NO: 39 and a nucleotide sequence encoding mouse Neu2 is depicted in SEQ ID NO: 43. The amino acid sequence of mouse Neu3 is depicted in SEQ ID NO: 40, and a nucleotide sequence encoding mouse Neu3 is depicted in SEQ ID NO: 44. The amino acid sequence of mouse Neu4 is depicted in SEQ ID NO: 41, and a nucleotide sequence encoding mouse Neu4 is depicted in SEQ ID NO: 45.

[0081] In certain embodiments, a sialidase portion of a sialidase-anti-PD-Ll fusion protein is derived from a prokaryotic sialidase. Exemplary prokaryotic sialidases include sialidases from Salmonella typhimurium and Vibrio cholera. The amino acid sequence of Salmonella typhimurium sialidase (St-sialidase) is depicted in SEQ ID NO: 30, and a nucleotide sequence encoding Salmonella typhimurium sialidase is depicted in SEQ ID NO: 6. The amino acid sequence of Vibrio cholera sialidase is depicted in SEQ ID NO: 36, and a nucleotide sequence encoding Vibrio cholera sialidase is depicted in SEQ ID NO: 37.

[0082] In certain embodiments, the sialidase portion of a sialidase-anti-PD-Ll fusion protein is a mutant sialidase, e.g ., a recombinant mutant human sialidase. In certain embodiments, the recombinant mutant human sialidase has about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, about 100%, or more than 100% of the enzymatic activity of a corresponding (or template) wild-type human sialidase.

[0083] In certain embodiments, the recombinant mutant human sialidase has the same substrate specificity as the corresponding wild-type human sialidase. In other embodiments, the recombinant mutant human sialidase has a different substrate specificity than the corresponding wild-type human sialidase. For example, in certain embodiments the recombinant mutant human sialidase can cleave a2,3, a2,6, and/or a2,8 linkages. In certain embodiments the sialidase can cleave a2,3 and a2,8 linkages.

[0084] In certain embodiments, the expression yield of the recombinant mutant human sialidase in mammalian cells, e.g. , HEK293 cells, CHO cells, murine myeloma cells (NS0, Sp2/0), or human fibrosarcoma cells (HT-1080), e.g, HEK293 cells, is greater than about 10%, about 20%, about 50%, about 75%, about 100%, about 150%, about 200%, about 250%, about 300%, about 400%, about 500%, about 600%, about 700%, about 800%, about 900%, or about 1,000% of the expression yield of the corresponding wild-type human sialidase.

[0085] In certain embodiments, the recombinant mutant human sialidase has about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, about 100%, or more than 100% of the enzymatic activity of a corresponding wild-type human sialidase, and the expression yield of the recombinant mutant human sialidase in mammalian cells, e.g., HEK293 cells, is greater than about 10%, about 20%, about 50%, about 75%, about 100%, about 150%, about 200%, about 250%, about 300%, about 400%, about 500%, about 600%, about 700%, about 800%, about 900%, or about 1,000% of the expression yield of a corresponding wild-type human sialidase.

[0086] In certain embodiments, the amino acid sequence of the recombinant mutant human sialidase has at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to the amino acid sequence of a corresponding wild-type human sialidase.

1. Substitution of Cysteine Residues

[0087] In certain embodiments, the recombinant mutant human sialidase comprises a

substitution of at least one cysteine (cys, C) residue. It has been discovered that certain cysteine residues in sialidases may inhibit expression of functional protein as a result of protein aggregation. Accordingly, in certain embodiments, the recombinant mutant human sialidase contains at least one mutation to remove a free cysteine (e.g, for Neul (SEQ ID NO: 7), a mutation of, for example, one or more of Cl l l, 017, 071, 083, C218, C240, C242, and C252; for Neu2 (SEQ ID NO: 1), a mutation of, for example, one or more of 025, 096, C219, Clll, C332, and C352; for Neu3 (SEQ ID NO: 8), a mutation of, for example, one or more of Cl, C90, C99, 006, 027, 036, 089, 094, C226, C242, C250, Clll, C119, C295, C356, C365, C368, C384, C383, C394, and C415; and for Neu4 (SEQ ID NO: 10), a mutation of, for example, one or more of C88, 025, 026, 086, 091, C211, C223, C239, C276, C437, C453, C480, and C481). Free cysteines can be substituted with any amino acid. In certain

embodiments, the free cysteine is substituted with serine (ser, S), isoleucine (iso, I), valine (val, V), phenylalanine (phe, F), leucine (leu, L), or alanine (ala, A). Exemplary cysteine

substitutions in Neu2 include C125A, 0251, C125S, C125V, C196A, C196L, C196V, C272S, CHIN , C332A, C332S, C332V, C352L, and C352V. [0088] In certain embodiments, the recombinant mutant human sialidase comprises two or more cysteine substitutions. Exemplary double or triple cysteine substitutions in Neu2 include: C125S and C332S; C272V and C332A; C272V and C332S; C332A and C352L; C125S and C196L; C196L and C352L; C196L and C332A; C332A and C352L; and C196L, C332A and C352L.

[0089] In certain embodiments, the recombinant mutant human sialidase is a Neu2 sialidase and comprises the substitutions C322A and C352L (SEQ ID NO: 5).

[0090] In certain embodiments, the sialidase contains an amino acid substitution at 2, 3, 4, 5, or 6 cysteines typically present in a human sialidase, e.g., Neu2 or Neu3.

[0091] In certain embodiments, the recombinant mutant human sialidase comprises a substitution or combination of substitutions corresponding to a substitution or combination of substitutions listed in TABLE 1 (amino acid positions corresponding to wild-type human Neu2 (SEQ ID NO: 1)).

TABLE 1

2. Substitutions of Residues to Increase pi and/or Decrease Hydrophobicitv

[0092] The isoelectric point (pi) of a protein is the pH at which the net charge is zero. The pi also generally indicates the pH at which the protein is least soluble, which may affect the ability to express and purify the protein. Generally, a protein has good solubility if its pi is greater than 2 units above the pH of the solution. Human Neu2 has a predicted pi of 7.5. Thus, human Neu2 is least soluble around neutral pH, which is undesirable because expression and physiological systems are at neutral pH. In contrast, the sialidase from Salmonella typhimurium (St-sialidase), which exhibits good solubility and recombinant expression, has a pi of 9.6. Accordingly, to increase expression of human Neu2 or the other human sialidases, a recombinant mutant human sialidase may be designed to contain one or more amino acid substitution(s) wherein the substitution(s) increase(s) the pi of the sialidase relative to a sialidase without the substitution. Additionally, decreasing the number of hydrophobic amino acids on the surface of a sialidase may improve expression of sialidase by, for example, reducing aggregation. Accordingly, to increase expression of human Neu2 or the other human sialidases, a recombinant mutant human sialidase may be designed to contain one or more amino acid substitution(s) wherein the substitution(s) decrease(s) the hydrophobicity of a surface of the sialidase relative to a sialidase without the substitution(s).

[0093] Accordingly, in certain embodiments, the recombinant mutant human sialidase comprises at least one amino acid substitution, wherein the substitution increases the isoelectric point (pi) of the sialidase and/or decreases the hydrophobicity of the sialidase relative to a sialidase without the substitution. This may be achieved by introducing one or more charged amino acids, for example, positively or negatively charged amino acids, into the recombinant sialidase. In certain embodiments, the amino acid substitution is to a charged amino acid, for example, a positively charged amino acid such as lysine (lys, K), histidine (his, H), or arginine (arg, R), or a negatively charged amino acid such as aspartic acid (asp, D) or glutamic acid (glu, E). In certain embodiments, the amino acid substitution is to a lysine residue. In certain embodiments, the substitution increases the pi of the sialidase to about 7.75, about 8, about 8.25, about 8.5, about 8.75, about 9, about 9.25, about 9.5, or about 9.75.

[0094] In certain embodiments, the amino acid substitution occurs at a surface exposed D or E amino acid, in a helix or loop, or in a position that has a K or R in the corresponding position of St-sialidase. In certain embodiments, the amino acid substitution occurs at an amino acid that is remote from the catalytic site or otherwise not involved in catalysis, an amino acid that is not conserved with the other human Neu proteins or with St-Sialidase or Clostridium NanH, or an amino acid that is not located in a domain important for function (e.g, an Asp-box or beta strand).

[0095] Exemplary amino acid substitutions in Neu2 that increase the isoelectric point (pi) of the sialidase and/or decrease the hydrophobicity of the sialidase relative to a sialidase without the substitution include A2E, A2K, D215K, V325E, V325K, E257K, and E319K. In certain embodiments, the recombinant mutant human sialidase comprises two or more amino acid substitutions, including, for example, A2K and V325E, A2K and V325K, E257K and V325K, A2K and E257K, and E257K and A2K and V325K.

[0096] In certain embodiments, the recombinant mutant human sialidase comprises a substitution or combination of substitutions corresponding to a substitution or combination of substitutions listed in TABLE 2 (amino acid positions corresponding to wild-type human Neu2 (SEQ ID NO: 1)).

TABLE 2

3. Addition of N-terminal Peptides and N- or C-terminal Substitutions

[0097] It has been discovered that the addition of a peptide sequence of two or more amino acids to the N-terminus of a human sialidase can improve expression and/or activity of the sialidase.

In certain embodiments, the peptide is at least 2 amino acids in length, for example, from 2 to 20, from 2 to 10, from 2 to 5, or 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 amino acids in length. In certain embodiments, the peptide may form, or have a propensity to form, an a-helix.

[0098] In mice, a Neu2 isoform (type B) found in thymus contains six amino acids not present in the canonical isoform of Neu2 found in skeletal muscle. In certain embodiments herein, the N- terminal six amino acids of the mouse thymus Neu2 isoform, MEDLRP (SEQ ID NO: 4), or variations thereof, can be added onto a human Neu, e.g., human Neu2. In certain embodiments, the recombinant mutant human sialidase comprises a peptide at least two amino acid residues in length covalently associated with an N-terminal amino acid of the sialidase. In certain embodiments the recombinant mutant human sialidase comprises the peptide MEDLRP (SEQ ID NO: 4) or EDLRP (SEQ ID NO: 3) covalently associated with an N-terminal amino acid of the sialidase. In certain embodiments, the sialidase may further comprise a cleavage site, e.g ., a proteolytic cleavage site, located between the peptide, e.g, MEDLRP (SEQ ID NO: 4) or EDLRP (SEQ ID NO: 3), and the remainder of the sialidase. In certain embodiments, the peptide, e.g., MEDLRP (SEQ ID NO: 4) or EDLRP (SEQ ID NO: 3), may be post- translationally cleaved from the remainder of the sialidase.

[0099] Alternatively to, or in combination with, the N-terminal addition, 1-5 amino acids of the 12 amino acid N-terminal region of the recombinant mutant human sialidase may be removed, e.g., the N-terminal methionine can be removed. In certain embodiments, if the recombinant mutant human sialidase is Neu2, the N-terminal methionine can be removed, the first five amino acids (MASLP; SEQ ID NO: 12) can be removed, or the second through fourth amino acids (ASLP; SEQ ID NO: 13) can be removed.

[00100] In certain embodiments, 1-5 amino acids of the 12 amino acid N-terminal region of the recombinant mutant human sialidase are substituted with MEDLRP (SEQ ID NO: 4), EDLRP (SEQ ID NO: 3), or TVEKSVVF (SEQ ID NO: 14). For example, in certain embodiments, if the recombinant mutant human sialidase is Neu2, the amino acids MASLP (SEQ ID NO: 12), ASLP (SEQ ID NO: 13) or M are substituted with MEDLRP (SEQ ID NO:

4), EDLRP (SEQ ID NO: 3) or TVEKSVVF (SEQ ID NO: 14).

[00101] Human sialidases have a b-propeller structure, characterized by 6 blade-shaped b- sheets arranged toroidally around a central axis. Generally, hydrophobic interactions between the blades of a b-propeller, including between the N- and C-terminal blades, enhance stability. Accordingly, in order to increase expression of human Neu2 or the other human sialidases, a recombinant mutant human sialidase can be designed comprising an amino acid substitution that increases hydrophobic interactions and/or hydrogen bonding between the N- and C-terminal b- propeller blades of the sialidase.

[00102] Accordingly, in certain embodiments, the recombinant mutant human sialidase comprises a substitution of at least one wild-type amino acid residue, wherein the substitution increases hydrophobic interactions and/or hydrogen bonding between the N- and C-termini of the sialidase relative to a sialidase without the substitution. In certain embodiments, the wild- type amino acid is substituted with asparagine (asn, N), lysine (lys, K), tyrosine (tyr, Y), phenylalanine (phe, F), or tryptophan (trp, W). Exemplary substitutions in Neu2 that increase hydrophobic interactions and/or hydrogen bonding between the N- and C-termini include L4N, L4K, V6Y, L7N, L4N and L7N, L4N and V6Y and L7N, V12N, V12Y, V12L, V6Y, V6F, or V6W. In certain embodiments, the sialidase comprises the V6Y substitution.

[00103] In certain embodiments, the recombinant mutant human sialidase comprises a combination of the above substitutions. For example, a recombinant mutant human Neu2 sialidase can comprise the additional amino acids MEDLRP (SEQ ID NO: 4), EDLRP (SEQ ID NO: 3), or TVEKSVVF (SEQ ID NO: 14) at the N-terminus and, in combination, can comprise at least one L4N, L4K, V6Y, L7N, L4N and L7N, L4N and V6Y and L7N, V12N, V12Y, V12L, V6Y, V6F, or V6W substitution. In certain embodiments, the amino acids MASLP (SEQ ID NO: 12), ASLP (SEQ ID NO: 13) or M of a recombinant mutant human Neu2 sialidase are replaced with MEDLRP (SEQ ID NO: 4), EDLRP (SEQ ID NO: 3) or TVEKSVVF (SEQ ID NO: 14) and the recombinant mutant human Neu2 sialidase also comprises at least one L4N, L4K, V6Y, L7N, L4N and L7N, L4N and V6Y and L7N, V12N, V12Y, V12L, V6Y, V6F, or V6W substitution.

[00104] In certain embodiments, the recombinant mutant human sialidase comprises a mutation or combination of mutations corresponding to a mutation or combination of mutations listed in TABLE 3 (amino acid positions corresponding to wild-type human Neu2 (SEQ ID NO: 1))·

TABLE 3

[00105] Additionally, in certain embodiments, the sialidase comprises a substitution or deletion of an N-terminal methionine at the N-terminus of the sialidase. For example, in certain embodiments, the sialidase comprises a substitution of a methionine residue at a position corresponding to position 1 of wild-type human Neu2 (SEQ ID NO: 1), e.g, the methionine at a position corresponding to position 1 of wild-type human Neu2 is substituted by alanine (MIA) or aspartic acid (MID). In other embodiments, the sialidase comprises a deletion of a methionine residue at a position corresponding to position 1 (DM1) of wild-type human Neu2 (SEQ ID NO: 1).

[00106] In certain embodiments, the recombinant mutant human sialidase comprises a substitution or combination of substitutions corresponding to a substitution or combination of substitutions listed in TABLE 4 (amino acid positions corresponding to wild-type human Neu2 (SEQ ID NO: 1)).

TABLE 4

4. Substitutions of Residues to Decrease Proteolytic Cleavage

[00107] It has been discovered that certain sialidases ( e.g ., human Neu2) are susceptible to cleavage by a protease (e.g., trypsin). As a result, proteolytic cleavage of the sialidase may occur during recombinant protein production, harvesting, purification, or formulation, during administration to a subject, or after administration to a subject. Accordingly, in certain embodiments, the recombinant mutant human sialidase comprises a substitution of at least one wild-type amino acid residue, wherein the substitution decreases cleavage of the sialidase by a protease (e.g, trypsin) relative to a sialidase without the substitution.

[00108] In certain embodiments, incubation of the recombinant mutant human sialidase with a protease (e.g, trypsin) results in from about 1% to about 50%, from about 1% to about 40%, from about 1%, to about 30%, from about 1% to about 20%, from about 1% to about 10%, from about 1% to about 5%, from about 5% to about 50%, from about 5% to about 40%, from about 5% to about 30%, from about 5% to about 20%, from about 5% to about 10%, from about 10% to about 50%, from about 10% to about 40%, from about 10% to about 30%, from about

10% to about 20%, from about 20% to about 50%, from about 20% to about 40%, from about

20% to about 30%, from about 30% to about 50%, from about 30% to about 40%, or from about

40% to about 50% of the proteolytic cleavage of a corresponding wild-type sialidase when incubated with the protease under the same conditions. In certain embodiments, incubation of the recombinant mutant human sialidase with a protease ( e.g trypsin) results in less than 50%, less than 40%, less than 30%, less than 10%, less than 5%, less than 3%, less than 1%, or less than 0.5% of the proteolytic cleavage of a corresponding wild-type sialidase when incubated with the protease under the same conditions. Proteolytic cleavage can be assayed by any method known in the art, including for example, by SDS-PAGE as described in Example 4 herein.

[00109] Exemplary substitutions that increase resistance to proteolytic cleavage include:

(i) a substitution of an alanine residue at a position corresponding to position 242 of wild-type human Neu2 (SEQ ID NO: 1), e.g., a substitution by cysteine (A242C), phenylalanine (A242F), glycine (A242G), histidine (A242H), isoleucine (A242I), lysine (A242K), leucine (A242L), methionine (A242M), asparagine (A242N), glutamine (A242Q), arginine (A242R), serine (A242S), valine (A242V), tryptophan (A242W), or tyrosine (A242Y); (ii) a substitution of an arginine residue at a position corresponding to position 243 of wild-type human Neu2 (SEQ ID NO: 1), e.g., a substitution by glutamic acid (R243E), histidine (R243H), asparagine (R243N), glutamine (R243Q), or lysine (R243K); (iii) a substitution of a valine residue at a position corresponding to position 244 of wild-type human Neu2 (SEQ ID NO: 1), e.g, a substitution by isoleucine (V244I), lysine (V244K), or proline (V244P); or (iv) a combination of any of the foregoing. In certain embodiments, the recombinant mutant human sialidase comprises a substitution selected from A242C, A242F, A242Y, and A242W. In certain embodiments, the recombinant mutant human sialidase comprises a substitution or a combination of substitutions corresponding to a substitution or combination of substitutions listed in TABLE 5 (amino acid positions corresponding to wild-type human Neu2 (SEQ ID NO: 1)). TABLE 5

[00110] Additional exemplary substitutions that increase resistance to proteolytic cleavage (and/or increase expression yield and/or enzymatic activity) include: (i) a substitution of a leucine residue at a position corresponding to position 240 of wild-type human Neu2 (SEQ ID NO: 1), e.g. , a substitution by aspartic acid (L240D), asparagine (L240N), or tyrosine (L240Y); (ii) a substitution of an alanine residue at a position corresponding to position 213 of wild-type human Neu2 (SEQ ID NO: 1), e.g., a substitution by cysteine (A213C), asparagine (A213N), serine (A213S), or threonine (A213T); (iii) a substitution of an arginine residue at a position corresponding to position 241 of wild-type human Neu2 (SEQ ID NO: 1), e.g, a substitution by alanine (R241A), aspartic acid (R241D), leucine (R241L), glutamine (R241Q). or tyrosine (R241 Y); (iv) a substitution of a serine residue at a position corresponding to position 258 of wild-type human Neu2 (SEQ ID NO: 1), e.g, a substitution by cysteine (S258C); (v) a substitution of a leucine residue at a position corresponding to position 260 of wild-type human Neu2 (SEQ ID NO: 1), e.g, a substitution by aspartic acid (L260D), phenylalanine (L260F), glutamine (L260Q), or threonine (L260T); (vi) a substitution of a valine residue at a position corresponding to position 265 of wild-type human Neu2 (SEQ ID NO: 1), e.g, a substitution by phenylalanine (V265F); or (vii) a combination of any of the foregoing. It is contemplated that, in certain embodiments, a substitution or a combination of substitutions at these positions may improve hydrophobic and/or aromatic interaction between secondary structure elements in the sialidase (e.g, between an a-helix and the nearest b-sheet) thereby stabilizing the structure and improving resistance to proteolytic cleavage.

[00111] In certain embodiments, the recombinant mutant sialidase comprises a mutation at position L240. In certain embodiments, the recombinant mutant sialidase comprises a combination of mutations at positions (i) A213 and A242, (ii) A213, A242, and S258, (iii) L240 and L260, (iv) R241 and A242, (v) A242 and L260, (vi) A242 and V265, or (vii) L240 and A242. In certain embodiments, the recombinant mutant human sialidase comprises a

combination of substitutions selected from (i) A213C, A242F, and S258C, (ii) A213C and A242F, (iii) A213T and A242F, (iv) R241Y and A242F, and (v) L240Y and A242F. In certain embodiments, the recombinant mutant human sialidase comprises a substitution or combination of substitutions corresponding to a substitution or combination of substitutions listed in TABLE 6 (amino acid positions corresponding to wild-type human Neu2 (SEQ ID NO: 1)).

TABLE 6

5. Other Substitutions

[00112] In certain embodiments, the recombinant mutant human sialidase comprises at least one of the following substitutions: I187K, A328E, K370N, or H210N. In certain embodiments, a recombinant mutant human Neu2 comprises the substitution of the amino acids GDYDAPTHQVQW (SEQ ID NO: 15) with the amino acids SMDQGSTW (SEQ ID NO: 16) or STDGGKTW (SEQ ID NO: 17). In certain embodiments, a recombinant mutant human Neu2 comprises the substitution of the amino acids PRPPAPEA (SEQ ID NO: 18) with the amino acids QTPLEAAC (SEQ ID NO: 19). In certain embodiments, a recombinant mutant human Neu2 comprises the substitution of the amino acids NPRPPAPEA (SEQ ID NO: 20) with the amino acids SQNDGES (SEQ ID NO: 21).

[00113] In certain embodiments, the recombinant mutant human sialidase comprises at least one substitution at a position corresponding to V212, A213, Q214, D215, T216, L217, E218, C219, Q220, V221, A222, E223, V224, E225, or T225.

[00114] In certain embodiments, the recombinant mutant human sialidase comprises an amino acid substitution at a position identified in TABLE 7 (amino acid positions corresponding to wild-type human Neu2 (SEQ ID NO: 1). In certain embodiments, the sialidase comprises an amino acid substitution identified in TABLE 7. In certain embodiments, the sialidase comprises a combination of any amino acid substitutions identified in TABLE 7.

TABLE 7

[00115] For example, in certain embodiments, the recombinant mutant human sialidase comprises: (a) a substitution of a proline residue at a position corresponding to position 5 of wild-type human Neu2 (P5); (b) a substitution of a lysine residue at a position corresponding to position 9 of wild-type human Neu2 (K9); (c) a substitution of a lysine residue at a position corresponding to position 44 of wild-type human Neu2 (K44); (d) a substitution of a lysine residue at a position corresponding to position 45 of wild-type human Neu2 (K45); (e) a substitution of a leucine residue at a position corresponding to position 54 of wild-type human Neu2 (L54); (f) a substitution of a proline residue at a position corresponding to position 62 of wild-type human Neu2 (P62); (g) a substitution of a glutamine residue at a position

corresponding to position 69 of wild-type human Neu2 (Q69); (h) a substitution of an arginine residue at a position corresponding to position 78 of wild-type human Neu2 (R78); (i) a substitution of an aspartic acid residue at a position corresponding to position 80 of wild-type human Neu2 (D80); (j) a substitution of an alanine residue at a position corresponding to position 93 of wild-type human Neu2 (A93); (k) a substitution of a glycine residue at a position corresponding to position 107 of wild-type human Neu2 (G107); (1) a substitution of a glutamine residue at a position corresponding to position 108 of wild-type human Neu2 (Q108); (m) a substitution of a glutamine residue at a position corresponding to position 112 of wild-type human Neu2 (Q112); (n) a substitution of a cysteine residue at a position corresponding to position 125 of wild-type human Neu2 (C125); (o) a substitution of a glutamine residue at a position corresponding to position 126 of wild-type human Neu2 (Q126); (p) a substitution of an alanine residue at a position corresponding to position 150 of wild-type human Neu2 (A150); (q) a substitution of a cysteine residue at a position corresponding to position 164 of wild-type human Neu2 (Cl 64); (r) a substitution of an arginine residue at a position corresponding to position 170 of wild-type human Neu2 (R170); (s) a substitution of an alanine residue at a position corresponding to position 171 of wild-type human Neu2 (A171); (t) a substitution of a glutamine residue at a position corresponding to position 188 of wild-type human Neu2 (Q188); (u) a substitution of an arginine residue at a position corresponding to position 189 of wild-type human Neu2 (R189); (v) a substitution of an alanine residue at a position corresponding to position 213 of wild-type human Neu2 (A213); (w) a substitution of a leucine residue at a position corresponding to position 217 of wild-type human Neu2 (L217); (x) a substitution of a glutamic acid residue at a position corresponding to position 225 of wild-type human Neu2 (E225); (y) a substitution of a histidine residue at a position corresponding to position 239 of wild-type human Neu2 (H239); (z) a substitution of a leucine residue at a position corresponding to position 240 of wild-type human Neu2 (L240); (aa) a substitution of an arginine residue at a position corresponding to position 241 of wild-type human Neu2 (R241); (bb) a substitution of an alanine residue at a position corresponding to position 242 of wild-type human Neu2 (A242); (cc) a substitution of a valine residue at a position corresponding to position 244 of wild-type human Neu2 (V244); (dd) a substitution of a threonine residue at a position corresponding to position 249 of wild-type human Neu2 (T249); (ee) a substitution of an aspartic acid residue at a position corresponding to position 251 of wild-type human Neu2 (D251); (ff) a substitution of a glutamic acid residue at a position corresponding to position 257 of wild-type human Neu2 (E257); (gg) a substitution of a serine residue at a position corresponding to position 258 of wild-type human Neu2 (S258); (hh) a substitution of a leucine residue at a position

corresponding to position 260 of wild-type human Neu2 (L260); (ii) a substitution of a valine residue at a position corresponding to position 265 of wild-type human Neu2 (V265); (jj) a substitution of a glutamine residue at a position corresponding to position 270 of wild-type human Neu2 (Q270); (kk) a substitution of a tryptophan residue at a position corresponding to position 292 of wild-type human Neu2 (W292); (11) a substitution of a serine residue at a position corresponding to position 301 of wild-type human Neu2 (S301); (mm) a substitution of a tryptophan residue at a position corresponding to position 302 of wild-type human Neu2 (W302); (nn) a substitution of a valine residue at a position corresponding to position 363 of wild-type human Neu2 (V363); or (oo) a substitution of a leucine residue at a position corresponding to position 365 of wild-type human Neu2 (L365); or a combination of any of the foregoing substitutions. For example, the sialidase may comprise a substitution of K9, P62, A93, Q216, A242, Q270, S301, W302, V363, or L365, or a combination of any of the foregoing substitutions.

[00116] In certain embodiments, in the sialidase: (a) the proline residue at a position corresponding to position 5 of wild-type human Neu2 is substituted by histidine (P5H); (b) the lysine residue at a position corresponding to position 9 of wild-type human Neu2 is substituted by aspartic acid (K9D); (c) the lysine residue at a position corresponding to position 44 of wild- type human Neu2 is substituted by arginine (K44R) or glutamic acid (K44E); (d) the lysine residue at a position corresponding to position 45 of wild-type human Neu2 is substituted by alanine (K45 A), arginine (K45R), or glutamic acid (K45E); (e) the leucine residue at a position corresponding to position 54 of wild-type human Neu2 is substituted by methionine (L54M); (f) the proline residue at a position corresponding to position 62 of wild-type human Neu2 is substituted by asparagine (P62N), aspartic acid (P62D), histidine (P62H), glutamic acid (P62E), glycine (P62G), serine (P62S), or threonine (P62T); (g) the glutamine residue at a position corresponding to position 69 of wild-type human Neu2 is substituted by histidine (Q69H); (h) the arginine residue at a position corresponding to position 78 of wild-type human Neu2 is substituted by lysine (R78K); (i) the aspartic acid residue at a position corresponding to position 80 of wild-type human Neu2 is substituted by proline (D80P); (j) the alanine residue at a position corresponding to position 93 of wild-type human Neu2 is substituted by glutamic acid (A93E) or lysine (A93K); (k) the glycine residue at a position corresponding to position 107 of wild-type human Neu2 is substituted by aspartic acid (G107D); (1) the glutamine residue at a position corresponding to position 108 of wild-type human Neu2 is substituted by histidine (Q108H); (m) the glutamine residue at a position corresponding to position 112 of wild-type human Neu2 is substituted by arginine (Q112R) or lysine (Q112K); (n) the cysteine residue at a position corresponding to position 125 of wild-type human Neu2 is substituted by leucine (C125L); (o) the glutamine residue at a position corresponding to position 126 of wild-type human Neu2 is substituted by leucine (Q126L), glutamic acid (Q126E), phenylalanine (Q126F), histidine (Q126H), isoleucine (Q126I), or tyrosine (Q126Y); (p) the alanine residue at a position corresponding to position 150 of wild-type human Neu2 is substituted by valine (A150V); (q) the cysteine residue at a position corresponding to position 164 of wild-type human Neu2 is substituted by glycine (C164G); (r) the arginine residue at a position corresponding to position 170 of wild-type human Neu2 is substituted by proline (R170P); (s) the alanine residue at a position corresponding to position 171 of wild-type human Neu2 is substituted by glycine (A171G); (t) the glutamine residue at a position corresponding to position 188 of wild-type human Neu2 is substituted by proline (Q188P); (u) the arginine residue at a position

corresponding to position 189 of wild-type human Neu2 is substituted by proline (R189P); (v) the alanine residue at a position corresponding to position 213 of wild-type human Neu2 is substituted by cysteine (A213C), asparagine (A213N), serine (A213S), or threonine (A213T); (w) the leucine residue at a position corresponding to position 217 of wild-type human Neu2 is substituted by alanine (L217A) or valine (L217V); (x) the threonine residue at a position corresponding to position 249 of wild-type human Neu2 is substituted by alanine (T249A); (y) the aspartic acid residue at a position corresponding to position 251 of wild-type human Neu2 is substituted by glycine (D251G); (z) the glutamic acid residue at a position corresponding to position 225 of wild-type human Neu2 is substituted by proline (E225P); (aa) the histidine residue at a position corresponding to position 239 of wild-type human Neu2 is substituted by proline (H239P); (bb) the leucine residue at a position corresponding to position 240 of wild- type human Neu2 is substituted by aspartic acid (L240D), asparagine (L240N), or tyrosine (L240Y); (cc) the arginine residue at a position corresponding to position 241 of wild-type human Neu2 is substituted by alanine (R241 A), aspartic acid (R241D), leucine (R241L), glutamine (R241Q). or tyrosine (R241Y); (dd) the alanine residue at a position corresponding to position 242 of wild-type human Neu2 is substituted by cysteine (A242C), phenylalanine (A242F), glycine (A242G), histidine (A242H), isoleucine (A242I), lysine (A242K), leucine (A242L), methionine (A242M), asparagine (A242N), glutamine (A242Q), arginine (A242R), serine (A242S), valine (A242V), tryptophan (A242W), or tyrosine (A242Y); (ee) the valine residue at a position corresponding to position 244 of wild-type human Neu2 is substituted by isoleucine (V244I), lysine (V244K), or proline (V244P); (ff) the glutamic acid residue at a position corresponding to position 257 of wild-type human Neu2 is substituted by proline (E257P); (gg) the serine residue at a position corresponding to position 258 is substituted by cysteine (S258C); (hh) the leucine residue at a position corresponding to position 260 of wild- type human Neu2 is substituted by aspartic acid (L260D), phenylalanine (L260F), glutamine (L260Q), or threonine (L260T); (ii) the valine residue at a position corresponding to position 265 of wild-type human Neu2 is substituted by phenylalanine (V265F); (jj) the glutamine residue at a position corresponding to position 270 of wild-type human Neu2 is substituted by alanine (Q270A), histidine (Q270H), phenylalanine (Q270F), proline (Q270P), serine (Q270S), or threonine (Q270T); (kk) the tryptophan residue at a position corresponding to position 292 of wild-type human Neu2 is substituted by arginine (W292R); (11) the serine residue at a position corresponding to position 301 of wild-type human Neu2 is substituted by alanine (S301 A), aspartic acid (S301D), glutamic acid (S301E), phenylalanine (S301F), glycine (S301G), histidine (S301H), isoleucine (S301I), lysine (S301K), leucine (S301L), methionine (S301M), asparagine (S301N), proline (S301P), glutamine (S301Q), arginine (S301R), threonine (S301T), valine (S301 V), tryptophan (S301W), or tyrosine (S301 Y); (mm) the tryptophan residue at a position corresponding to position 302 of wild-type human Neu2 is substituted by alanine (W302A), aspartic acid (W302D), glutamic acid (W302E), phenylalanine (W302F), glycine (W302G), histidine (W302H), isoleucine (W302I), lysine (W302K), leucine (W302L), methionine (W302M), asparagine (W302N), proline (W302P), glutamine (W302Q), arginine (W302R), serine (W302S), threonine (W302T), valine (W302V), or tyrosine (W302Y); (nn) the valine residue at a position corresponding to position 363 of wild-type human Neu2 is substituted by arginine (V363R); or (oo) the leucine residue at a position corresponding to position 365 of wild-type human Neu2 is substituted by glutamine (L365Q), histidine (L365H), isoleucine (L365I), lysine (L365K) or serine (L365S); or the sialidase comprises a combination of any of the foregoing substitutions. For example, the sialidase may comprise a substitution selected from K9D, P62G, P62N, P62S, P62T, D80P, A93E, Q126H, Q126Y, R189P, H239P, A242T, Q270A, Q270S, Q270T, S301A, S301R, W302K, W302R, V363R, and L365I, or a combination of any of the foregoing substitutions.

[00117] In certain embodiments, the recombinant mutant human sialidase comprises a deletion of a leucine residue at a position corresponding to position 184 of wild-type human Neu2 (AL l 84), a deletion of a histidine residue at a position corresponding to position 185 of wild-type human Neu2 (DH185), a deletion of a proline residue at a position corresponding to position 186 of wild-type human Neu2 (DR186), a deletion of an isoleucine residue at a position corresponding to position 187 of wild-type human Neu2 (DI187), and a deletion of a glutamine residue at a position corresponding to position 184 of wild-type human Neu2 (AQ l 88), or a combination of any of the foregoing deletions.

[00118] In certain embodiments, the recombinant mutant human sialidase comprises an insertion between a threonine residue at a position corresponding to position 216 of wild-type human Neu2 and a leucine residue at a position corresponding to position 217 of wild-type human Neu2, for example, an insertion of an amino acid selected from S, T, Y, L, F, A, P, V, I, N, D, and H.

[00119] Additional exemplary sialidase mutations, and combinations of sialidase mutations, are described in International (PCT) Patent Application No. PCT/US2019/012207, filed January 3, 2019, including in the Detailed Description in the section entitled“I.

Recombinant Human Sialidases,” and in the Examples in Examples 1, 2, 3, 4, 5, and 6.

6. Combinations of Substitutions

[00120] In certain embodiments, the recombinant mutant human sialidase comprises a combination of any of the mutations contemplated herein. For example, the recombinant mutant sialidase enzyme may comprise a combination of 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or more of the mutations contemplated herein. It is contemplated that the recombinant mutant sialidase enzyme may comprise 1-15, 1-10, 1-7, 1-6, 1-5, 1-4, 1-3, 1-2, 2-15, 2-10, 2-7, 2-6, 2-5, 2-4, 2-3, 3-15, 3-10, 3-7, 3-6, 3-5, or 3-4 of the mutations contemplated herein. [00121] For example, the recombinant mutant sialidase enzyme may comprise a Ml deletion (DM1), MIA substitution, MID substitution, V6Y substitution, K9D substitution, P62G substitution, P62N substitution, P62S substitution, P62T substitution, A93E substitution, I187K substitution, Q270A substitution, S301R substitution, W302K substitution, C332A substitution, V363R substitution, L365I substitution, or a combination of any of the foregoing.

[00122] In certain embodiments, the recombinant mutant sialidase enzyme comprises a Ml deletion (DM1), MIA substitution, MID substitution, V6Y substitution, I187K substitution, C332A substitution, or a combination of any of the foregoing. For example, the recombinant mutant sialidase enzyme may comprise a combination of mutations selected from: MIA and V6Y; MIA and I187K; MIA and C332A; MID and V6Y; MID and I187K; MID and C332A; DM1 and V6Y; DM1 and I187K; DM1 and C332A; V6Y and I187K; V6Y and C332A; I187K and C332A; MIA, V6Y, and I187K; MIA, V6Y, and C332A; MIA, I187K, and C332A; MID, V6Y, and I187K; MID, V6Y, and C332A; MID, I187K, and C332A; DM1, V6Y, and I187K; DM1, V6Y, and C332A; DM1, 1187K, and C332A; V6Y, I187K, and C332A; MIA, V6Y, I187K, and C332A; MID, V6Y, I187K, and C332A; and DM1, V6Y, I187K, and C332A.

[00123] In certain embodiments, the recombinant mutant sialidase enzyme comprises (i) an amino acid substitution identified in TABLE 7, or a combination of any amino acid substitutions identified in TABLE 7, and (ii) an Ml deletion (DM1), MIA substitution, MID substitution, V6Y substitution, I187K substitution, C332A substitution, or a combination of any of the foregoing. For example, the recombinant mutant sialidase enzyme may comprise (i) an amino acid substitution identified in TABLE 7, or a combination of any amino acid substitutions identified in TABLE 7, and (ii) a combination of mutations selected from: MIA and V6Y; MIA and I187K; MIA and C332A; MID and V6Y; MID and I187K; MID and C332A; DM1 and V6Y; DM1 and I187K; DM1 and C332A; V6Y and I187K; V6Y and C332A; I187K and C332A; MIA, V6Y, and I187K; MIA, V6Y, and C332A; MIA, I187K, and C332A; MID, V6Y, and I187K; MID, V6Y, and C332A; MID, I187K, and C332A; DM1, V6Y, and I187K; DM1, V6Y, and C332A; DM1, 1187K, and C332A; V6Y, I187K, and C332A; MIA, V6Y, I187K, and C332A; MID, V6Y, I187K, and C332A; and DM1, V6Y, I187K, and C332A.

[00124] In certain embodiments, the recombinant mutant sialidase enzyme comprises: (a) the MID, V6Y, P62G, A93E, I187K, and C332A substitutions; (b) the MID, V6Y, K9D, A93E, I187K, C332A, V363R, and L365I substitutions; (c) the MID, V6Y, P62N, I187K, and C332A substitutions; (d) the MID, V6Y, I187K, Q270A, S301R, W302K, and C332A substitutions; (e) the MID, V6Y, P62S, I187K, Q270A, S301R, W302K, and C332A substitutions; (f) the MID, V6Y, P62T, I187K, Q270A, S301R, W302K, and C332A substitutions; (g) the MID, V6Y, P62N, I187K, Q270A, S301R, W302K, and C332A substitutions; (h) the MID, V6Y, P62G, A93E, I187K, S301A, W302R, and C332A substitutions; (i) the MID, V6Y, P62G, A93E, Q126Y, I187K, Q270T, and C332A substitutions; G) the MID, V6Y, P62G, A93E, Q126Y, I187K, and C332A substitutions; or (k) the MID, V6Y, P62G, A93E, Q126Y, I187K, A242F,

Q270T, and C332A substitutions.

[00125] In certain embodiments, the recombinant mutant human sialidase comprises a substitution of a serine residue at a position corresponding to position 301 of wild-type human Neu2 (S301) in combination with a substitution of a tryptophan residue at a position

corresponding to position 302 of wild-type human Neu2 (W302). For example, the recombinant mutant human sialidase may comprise a combination of substitutions corresponding to a combination of substitutions listed in a row of TABLE 8 (amino acid positions corresponding to wild-type human Neu2 (SEQ ID NO: 1)). For example, the recombinant mutant human sialidase may comprise: the S301K and W302R substitutions; the S301K and W302K substitutions; or the S301A and W302S substitutions.

TABLE 8

[00126] In certain embodiments, the recombinant mutant human sialidase comprises a combination of substitutions corresponding to a combination of substitutions listed in a row of TABLE 9 (amino acid positions corresponding to wild-type human Neu2 (SEQ ID NO: 1)).

TABLE 9

[00127] In certain embodiments, the recombinant mutant human sialidase comprises the amino acid sequence of any one of SEQ ID NOs: 48-62, 94, 97, 100, or 126, or an amino acid sequence that has at least 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to any one of SEQ ID NOs: 48-62, 94, 97, 100, or 126.

[00128] In certain embodiments, the recombinant mutant human sialidase comprises the amino acid sequence of

X ₁ X ₂ SX ₃ X ₄ X ₅ LQX ₆ ESVFQSGAHAYRI PALLYLPGQQSLLAFAEQRASX ₇ X ₈ DEHAEL IVX ₉ RRGD

YDAX10THQVQWX11AQEWAQAX12LDGHRSMNPCPLYDX13QTGTLFLFFIAI PX14X15VTEX16Q

QLQTRANVTRLX17X18VTS TDHGRTWS S PRDLTDAAI GPX19YREWS T FAVGPGHX20LQLHDRX21 RSLWPAYAYRKLHPX ₂₂ QRP I PSAFX ₂₃ FLSHDHGRTWARGHFVAQDTX ₂₄ ECQVAEVETGEQRV

VTLNARSHLRARVQAQSX ₂₅ NX ₂₆ GLDFQX ₂₇ SQLVKKLVEPPPX ₂₈ GX ₂₉ QGSVI S FPS PRSGPGS P

AQX ₃₀ LLYTHPTHX ₃₁ X ₃₂ QRADLGAYLNPRPPAPEAWSEPX ₃₃ LLAKGSX ₃₄ AYSDLQSMGTGPDGS

PLFGX ₃₅ LYEANDYEE IX ₃₆ FX ₃₇ MFTLKQAFPAEYLPQ

(SEQ ID NO: 47), wherein Xi is Ala, Arg, Asn, Asp, Gin, Glu, Gly, His, Leu, Lys, Met, Phe, Thr, Val, or not present, X ₂ is Ala or Lys, X ₃ is Asn or Leu, X ₄ is Pro or His, X ₅ is Phe, Trp, Tyr or Val, X ₍ , is Lys or Asp, X ₇ is Lys, Arg, or Glu. Xx is Lys, Ala, Arg, or Glu, X ₉ is Leu or Met,

X ₁₀ is Pro, Asn, Asp, His, Glu, Gly, Ser or Thr, Xu is Gin or His, X ₁₂ is Arg or Lys, X ₁₃ is Ala, Glu or Lys, X ₁₄ is Gly or Asp, X ₁₅ is Gin or His, X½ is Gin, Arg, or Lys, X ₁₇ is Ala, Cys, lie, Ser, Val, or Leu, Xis is Gin or Leu, X ₁₉ is Ala or Val, X ₂₀ is Cys or Gly, X ₂₁ is Ala or Gly, X ₂₂ is Arg, lie, or Lys, X ₂₃ is Ala, Cys, Leu, or Val, X ₂₄ is Leu, Ala, or Val, X ₂₅ is Thr or Ala, X ₂₆ is Asp or Gly, X ₂₇ is Glu or Lys, X ₂₈ is Gin, Ala, His, Phe, or Pro, X ₂₉ is Cys or Val, X ₃₀ is Trp or Arg, X ₃₁ is Ser or Arg, X ₃₂ is Trp or Lys, X ₃₃ is Lys or Val, X ₃₄ is Ala, Cys, Ser, or Val, X ₃₅ is Cys, Leu, or Val, X _{36 IS} Val or Arg, and X _{37 IS} Leu, Gin, His, He, Lys, or Ser, and the sialidase comprises at least one mutation relative to wild-type human Neu2 (SEQ ID NO: 1).

[00129] In certain embodiments, the recombinant mutant human sialidase comprises the amino acid sequence of

X1ASLPX2LQX3ESVFQSGAHAYRI PALLYLPGQQSLLAFAEQRASKKDEHAEL IVLRRGDYDAX4

THQVQWQAQEWAQARLDGHRSMNPCPLYDX ₅ QTGTLFLFFIAI PGQVTEQQQLQTRANVTRLCQ

VT S TDHGRTWS S PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPXeQRP

I PSAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQS TNDGLD

FQESQLVKKLVEPPPX ₇ GCQGSVI S FPS PRSGPGS PAQWLLYTHPTHX ₈ X ₉ QRADLGAYLNPRPP

APEAWSEPVLLAKGSX ₁₀ AYSDLQSMGTGPDGS PLFGCLYEANDYEE IX ₁₁ FX ₁₂ MFTLKQAFPAE

YLPQ

(SEQ ID NO: 46), wherein Xi is Ala, Arg, Asn, Asp, Gin, Glu, Gly, His, Leu, Lys, Met, Phe, Thr, Val, or not present, X ₂ is Phe, Trp, Tyr or Val, X ₃ is Lys or Asp, X ₄ is Pro, Asn, Asp, His, Glu, Gly, Ser or Thr, X ₅ is Ala, Glu, or Lys, C _ό is Arg, He, or Lys, X ₇ is Gin, Ala, His, Phe, or Pro, X ₈ is Ser or Arg, X ₉ is Trp or Lys, X ₁₀ is Ala, Cys, Ser, or Val, Xu is Val or Arg, and X ₁₂ is Leu, Gin, His, He, Lys, or Ser, and the sialidase comprises at least one mutation relative to wild- type human Neu2 (SEQ ID NO: 1). In certain embodiments, Xi is Ala, Asp, Met, or not present, X ₂ is Tyr or Val, X ₃ is Lys or Asp, X ₄ is Pro, Asn, Gly, Ser or Thr, X ₅ is Ala or Glu, C _ό is He or Lys, X ₇ is Gin or Ala, Xs is Ser or Arg, X ₉ is Trp or Lys, X ₁₀ is Ala or Cys, Xu is Val or Arg, and X _{12 IS} Leu or He.

[00130] In certain embodiments, the recombinant mutant human sialidase comprises the amino acid sequence of

X ₁ X ₂ SX ₃ X ₄ X ₅ LQX ₆ ESVFQSGAHAYRI PALLYLPGQQSLLAFAEQRASX ₇ X ₈ DEHAEL IVX ₉ RRGD

YDAX10THQVQWX11AQEWAQAX12LX13GHRSMNPCPLYDX14QTGTLFLFFIAI PX15X16VTEX17

QQLQTRANVTRLX18X19VTS TDHGRTWS S PRDLTDAAI GPX20YREWS T FAVGPGHX21LQLHDX22 X ₂₃ RSLWPAYAYRKLHPX ₂₄ X ₂₅ X ₂₆ PI PSAFX ₂₇ FLSHDHGRTWARGHFVX ₂₈ QDTX ₂₉ ECQVAEVX

₃₀ TGEQRWTLNARSX ₃₁ X ₃₂ X ₃₃ X ₃₄ RX ₃₅ QAQSX ₃₆ NX ₃₇ GLDFQX ₃₈ X ₃₉ QX ₄₀ VKKL

X ₄₁ EPPPX ₄₂ GX ₄₃ QGSVI S FPS PRSGPGS PAQX ₄₄ LLYTHPTHX ₄₅ X ₄₆ QRADLGAYLNPRPPAPEA

WSEPX ₄₇ LLAKGSX ₄₈ AYSDLQSMGTGPDGS PLFGX ₄₉ LYEANDYEE IX ₅₀ FX ₅₁ MFTLKQAFPAEYL

PQ

(SEQ ID NO: 120), wherein Xi is Ala, Arg, Asn, Asp, Gin, Glu, Gly, His, Leu, Lys, Met, Phe, Thr, Val, or not present, X ₂ is Ala or Lys, X ₃ is Asn or Leu, X ₄ is Pro or His, X ₅ is Phe, Trp, Tyr or Val, X ₍ , is Lys or Asp, X ₇ is Lys, Arg, or Glu, Xx is Lys, Ala, Arg, or Glu, X ₉ is Leu or Met,

X ₁₀ is Pro, Asn, Asp, His, Glu, Gly, Ser or Thr, Xu is Gin or His, X ₁₂ is Arg or Lys, X ₁₃ is Asp or Pro, Xi ₄ is Ala, Glu or Lys, X ₁₅ is Gly or Asp, X½ is Gin or His, X ₁₇ is Gin, Arg, or Lys, Xis is Ala, Cys, lie, Ser, Val, or Leu, X ₁₉ is Gin, Leu, Glu, Phe, His, He, Leu, or Tyr, X ₂₀ is Ala or Val, X ₂₁ is Cys or Gly, X ₂₂ is Arg or Pro, X ₂₃ is Ala or Gly, X ₂₄ is Arg, He, or Lys, X ₂₅ is Gin or Pro, X ₂₆ is Arg or Pro, X ₂₇ is Ala, Cys, Leu, or Val, X ₂₈ is Ala, Cys, Asn, Ser, or Thr, X ₂₉ is Leu, Ala, or Val, X ₃₀ is Glu or Pro, X ₃₁ is His or Pro, X ₃₂ is Leu, Asp, Asn, or Tyr, X ₃₃ is Arg, Ala, Asp, Leu, Gin, or Tyr, X ₃₄ is Ala, Cys, Phe, Gly, His, He, Lys, Leu, Met, Asn, Gin, Arg, Ser, Val, Trp, or Tyr, X ₃₅ is Val, He, or Lys, X ₃₆ is Thr or Ala, X ₃₇ is Asp or Gly, X ₃₈ is Glu, Lys, or Pro, X ₃₉ is Ser or Cys, X ₄₀ is Leu, Asp, Phe, Gin, or Thr, X ₄₁ is Val or Phe, X ₄₂ is Gin, Ala, His, Phe, Pro, Ser, or Thr, X ₄₃ is Cys or Val, X ₄₄ is Trp or Arg, X ₄₅ is Ser, Arg, Ala, Asp, Glu, Phe, Gly, His,

He, Lys, Leu, Met, Asn, Pro, Gin, Thr, Val, Trp, or Tyr, X _{46 IS} Trp, Lys, Ala, Asp, Glu, Phe, Gly, His, He, Lys, Leu, Met, Asn, Pro, Gin, Arg, Ser, Thr, Val, or Tyr, X47 IS Lys or Val, X48 IS Ala, Cys, Ser, or Val, X ₄₉ is Cys, Leu, or Val, X ₅₀ is Val or Arg, and X ₅₁ is Leu, Gin, His, He, Lys, or Ser, and the sialidase comprises at least one mutation relative to wild-type human Neu2 (SEQ ID NO: 1).

[00131] In certain embodiments, the recombinant mutant human sialidase comprises the amino acid sequence of

X1ASLPX2LQX3ESVFQSGAHAYRI PALLYLPGQQSLLAFAEQRASKKDEHAEL IVLRRGDYDAX4

THQVQWQAQEWAQARLDGHRSMNPCPLYDX ₅ QTGTLFLFFIAI PGQVTEQQQLQTRANVTRLCX

₆ VT S TDHGRTWS S PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPX ₇ QR

P I PSAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRXsRVQAQS TNDGL

DFQESQLVKKLVEPPPX ₉ GCQGSVI S FPS PRSGPGS PAQWLLYTHPTHX ₁₀ X ₁₁ QRADLGAYLNPR

PPAPEAWSEPVLLAKGSX ₁₂ AYSDLQSMGTGPDGS PLFGCLYEANDYEE IX ₁₃ FX ₁₄ MFTLKQAFP

AEYLPQ

(SEQ ID NO: 119), wherein Xi is Ala, Arg, Asn, Asp, Gin, Glu, Gly, His, Leu, Lys, Met, Phe,

Thr, Val, or not present, X ₂ is Phe, Trp, Tyr or Val, X ₃ is Lys or Asp, X ₄ is Pro, Asn, Asp, His,

Glu, Gly, Ser or Thr, X ₅ is Ala, Glu, or Lys, C _ό is Gin, Leu, Glu, Phe, His, He, Leu, or Tyr, X ₇ is

Arg, He, or Lys, Xs is Ala, Cys, Phe, Gly, His, He, Lys, Leu, Met, Asn, Gin, Arg, Ser, Val, Trp, or Tyr, X9 IS Gin, Ala, His, Phe, Pro, Ser, or Thr, Xio is Ser, Arg, Ala, Asp, Glu, Phe, Gly, His,

He, Lys, Leu, Met, Asn, Pro, Gin, Thr, Val, Trp, or Tyr, Xu is Trp, Lys, Ala, Asp, Glu, Phe, Gly, His, He, Lys, Leu, Met, Asn, Pro, Gin, Arg, Ser, Thr, Val, or Tyr, Xo is Ala, Cys, Ser, or Val, Xi ₃ is Val or Arg, and Xi4 is Leu, Gin, His, He, Lys, or Ser, and the sialidase comprises at least one mutation relative to wild-type human Neu2 (SEQ ID NO: 1). In certain embodiments, Xi is Ala, Asp, Met, or not present, X2 is Tyr or Val, X3 is Lys or Asp, X4 is Pro, Asn, Gly, Ser or Thr, X5 is Ala or Glu, Xr, is Gin or Tyr, X7 is He or Lys, Xx is Ala or Thr, X9 is Gin, Ala, or Thr, X10 is Ser, Arg, or Ala, Xu is Trp, Lys, or Arg, X12 is Ala or Cys, X13 is Val or Arg, and X14 is Leu or He.

[00132] In certain embodiments, the recombinant mutant human sialidase comprises a conservative substitution relative to a recombinant mutant human sialidase sequence disclosed herein. As used herein, the term“conservative substitution” refers to a substitution with a structurally similar amino acid. For example, conservative substitutions may include those within the following groups: Ser and Cys; Leu, He, and Val; Glu and Asp; Lys and Arg; Phe, Tyr, and Trp; and Gin, Asn, Glu, Asp, and His. Conservative substitutions may also be defined by the BLAST (Basic Local Alignment Search Tool) algorithm, the BLOSUM substitution matrix ( e.g ., BLOSUM 62 matrix), or the PAM substitution^ matrix (e.g, the PAM 250 matrix).

[00133] Sequence identity may be determined in various ways that are within the skill of a person skilled in the art, e.g. , using publicly available computer software such as BLAST, BLAST-2, ALIGN or Megalign (DNASTAR) software. BLAST (Basic Local Alignment Search Tool) analysis using the algorithm employed by the programs blastp, blastn, blastx, tblastn and tblastx (Karlin et a/., (1990) PROC. NATL. ACAD. SCI. USA 87:2264-2268; Altschul, (1993) J. MOL. EVOL. 36:290-300; Altschul e /., (1997) NUCLEIC ACIDS RES. 25:3389-3402,

incorporated by reference herein) are tailored for sequence similarity searching. For a discussion of basic issues in searching sequence databases see Altschul el a/., (1994) NATURE GENETICS 6: 119-129, which is fully incorporated by reference herein. Those skilled in the art can determine appropriate parameters for measuring alignment, including any algorithms needed to achieve maximal alignment over the full length of the sequences being compared. The search parameters for histogram, descriptions, alignments, expect (i.e., the statistical significance threshold for reporting matches against database sequences), cutoff, matrix and filter are at the default settings. The default scoring matrix used by blastp, blastx, tblastn, and tblastx is the BLOSUM62 matrix (Henikoff et a/., (1992) PROC. NATL. ACAD. SCI. USA 89:10915-10919, fully incorporated by reference herein). Four blastn parameters may be adjusted as follows: Q=10 (gap creation penalty); R=10 (gap extension penalty); wink=l (generates word hits at every wink.sup.th position along the query); and gapw=16 (sets the window width within which gapped alignments are generated). The equivalent blastp parameter settings may be Q=9; R=2; wink=l; and gapw=32. Searches may also be conducted using the NCBI (National Center for Biotechnology Information) BLAST Advanced Option parameter ( e.g . : -G, Cost to open gap [Integer]: default = 5 for nucleotides/ 11 for proteins; -E, Cost to extend gap [Integer]: default =

2 for nucleotides/ 1 for proteins; -q, Penalty for nucleotide mismatch [Integer]: default = -3; -r, reward for nucleotide match [Integer]: default = 1; -e, expect value [Real]: default = 10; -W, wordsize [Integer]: default = 11 for nucleotides/ 28 for megablast/ 3 for proteins; -y, Dropoff (X) for blast extensions in bits: default = 20 for blastn/ 7 for others; -X, X dropoff value for gapped alignment (in bits): default = 15 for all programs, not applicable to blastn; and -Z, final X dropoff value for gapped alignment (in bits): 50 for blastn, 25 for others). ClustalW for pairwise protein alignments may also be used (default parameters may include, e.g., Blosum62 matrix and Gap Opening Penalty = 10 and Gap Extension Penalty = 0.1). A Bestfit comparison between sequences, available in the GCG package version 10.0, uses DNA parameters GAP=50 (gap creation penalty) and LEN=3 (gap extension penalty). The equivalent settings in Bestfit protein comparisons are GAP=8 and LEN=2.

b. Antibody Portion

[00134] As used herein, unless otherwise indicated, the term“antibody” is understood to mean an intact antibody (e.g, an intact monoclonal antibody), or a fragment thereof, such as a Fc fragment of an antibody (e.g, an Fc fragment of a monoclonal antibody), or an antigen-binding fragment of an antibody (e.g, an antigen-binding fragment of a monoclonal antibody), including an intact antibody, antigen-binding fragment, or Fc fragment that has been modified, engineered, or chemically conjugated. Examples of antigen-binding fragments include Fab, Fab’, (Fab’)2,

Fv, single chain antibodies (e.g, scFv), minibodies, and diabodies. Examples of antibodies that have been modified or engineered include chimeric antibodies, humanized antibodies, and multispecific antibodies (e.g, bispecific antibodies). An example of a chemically conjugated antibody is an antibody conjugated to a toxin moiety.

[00135] In certain embodiments, the fusion protein comprises an immunoglobulin Fc domain. As used herein, unless otherwise indicated, the term“immunoglobulin Fc domain” refers to a fragment of an immunoglobulin heavy chain constant region which, either alone or in

combination with a second immunoglobulin Fc domain, is capable of binding to an Fc receptor. An immunoglobulin Fc domain may include, e.g., immunoglobulin CH2 and CH3 domains. An immunoglobulin Fc domain may include, e.g, immunoglobulin CH2 and CH3 domains and an immunoglobulin hinge region. Boundaries between immunoglobulin hinge regions, CH2, and CH3 domains are well known in the art, and can be found, e.g ., in the PRO SITE database (available on the world wide web at prosite.expasy.org).

[00136] In certain embodiments, the immunoglobulin Fc domain is derived from a human IgGl, IgG2, IgG3, IgG4, IgAl, IgA2, IgD, IgE, and IgM Fc domain. A single amino acid substitution (S228P according to Rabat numbering; designated IgG4Pro) may be introduced to abolish the heterogeneity observed in recombinant IgG4 antibody. See Angal, S. et al. (1993) MOL.

IMMUNOL. 30: 105-108.

[00137] In certain embodiments, the immunoglobulin Fc domain is derived from a human IgGl isotype or another isotype that elicits antibody-dependent cell-mediated cytotoxicity (ADCC) and/or complement mediated cytotoxicity (CDC). In certain embodiments, the immunoglobulin Fc domain is derived from a human IgGl isotype (e.g., SEQ ID NO: 31 or SEQ ID NO: 5).

[00138] In certain embodiments, the immunoglobulin Fc domain is derived from a human IgG4 isotype or another isotype that elicits little or no antibody-dependent cell-mediated cytotoxicity (ADCC) and/or complement mediated cytotoxicity (CDC). In certain embodiments, the immunoglobulin Fc domain is derived from a human IgG4 isotype.

[00139] In certain embodiments, the immunoglobulin Fc domain comprises either a“knob” mutation, e.g, T366Y, or a“hole” mutation, e.g, Y407T, for heterodimerization with a second polypeptide (residue numbers according to EU numbering, Rabat, E.A., et al. (1991) SEQUENCES OF PROTEINS OF IMMUNOLOGICAL INTEREST, FIFTH EDITION, U.S. Department of Health and Human Services, NIH Publication No. 91-3242).

[00140] In certain embodiments, the fusion protein comprises an immunoglobulin antigen binding domain. The inclusion of such a domain may improve targeting of a fusion protein to a sialylated cancer cell, e.g., a PD-L1 expressing cancer cell, and/or to the tumor

microenvironment. As used herein, unless otherwise indicated, the term“immunoglobulin antigen-binding domain” refers to a polypeptide that, alone or in combination with another immunoglobulin antigen-binding domain, defines an antigen-binding site. Exemplary immunoglobulin antigen-binding domains include, for example, immunoglobulin heavy chain variable region and an immunoglobulin light chain variable region, where the variable regions together define an antigen binding site, e.g, an anti-PD-Ll antigen binding site.

[00141] In certain embodiments, the immunoglobulin antigen-binding domain is derived from an anti-PD-Ll antibody. Exemplary anti-PD-Ll antibodies are described, for example, in U.S.

Patent Nos. 9,273,135, 7,943,743, 9,175,082, 8,741,295, 8,552,154, and 8,217,149. Exemplary anti-PD-Ll antibodies include, atezolizumab (Tecentriq®, Genentech), durvalumab (AstraZeneca), MEDI4736, avelumab, CSIOOI (CStone Therapeutics), KL-A167, CK-301 (Checkpoint Therapeutics), TQB2450, KN035, SHR-1316, STI-A1014, BGB-A333, MSB2311, HLX-20 and BMS-936559 by Bristol-Myers Squibb.

[00142] In certain embodiments, the immunoglobulin antigen-binding domain is derived from avelumab. The avelumab heavy chain amino acid sequence is depicted in SEQ ID NO: 63, and the avelumab light chain amino acid sequence is depicted in SEQ ID NO: 64. The amino acid sequence of an exemplary scFv derived from avelumab is depicted in SEQ ID NO: 125.

c. Linker

[00143] In certain embodiments, the sialidase portion of the fusion protein can be linked or fused directly to the anti-PD-Ll antibody portion ( e.g immunoglobulin Fc domain and/or immunoglobulin antigen-binding domain) of the fusion protein. In other embodiments, the sialidase portion can be covalently bound to the anti-PD-Ll antibody portion by a linker.

[00144] The linker may couple, with one or more natural amino acids, the sialidase, or functional fragment thereof, and the antibody portions or fragments, where the amino acid (for example, a cysteine amino acid) may be introduced by site-directed mutagenesis. The linker may include one or more unnatural amino acids. It is contemplated that, in certain

circumstances, a linker containing for example, one or more sulfhydryl reactive groups (e.g., a maleimide) may covalently link a cysteine in the sialidase portion or the antibody portion that is a naturally occurring cysteine residue or is the product of site-specific mutagenesis.

[00145] The linker may be a cleavable linker or a non-cleavable linker. Optionally or in addition, the linker may be a flexible linker or an inflexible linker.

[00146] The linker should be a length sufficiently long to allow the sialidase and the antibody portions to be linked without steric hindrance from one another and sufficiently short to retain the intended activity of the fusion protein. The linker preferably is sufficiently hydrophilic to avoid or minimize instability of the fusion protein. The linker preferably is sufficiently hydrophilic to avoid or minimize insolubility of the fusion protein. The linker should be sufficiently stable in vivo (e.g, it is not cleaved by serum, enzymes, etc.) to permit the fusion protein to be operative in vivo.

[00147] The linker may be from about 1 angstroms (A) to about 150 A in length, or from about 1 A to about 120 A in length, or from about 5 A to about 110 A in length, or from about 10 A to about 100 A in length. The linker may be greater than about 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 27, 30 or greater angstroms in length and/or less than about 110,

100, 90, 85, 80, 75, 70, 65, 60, 55, 50, 45, 43, 42, 41, 40, 39, 38, 37, 36, 35, 34, 33, 32, 31, or fewer A in length. Furthermore, the linker may be about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110, and 120 A in length.

[00148] In certain embodiments, the linker comprises a polypeptide linker that connects or fuses the sialidase portion of the fusion protein to the anti-PD-Ll antibody portion ( e.g ., immunoglobulin Fc domain and/or immunoglobulin antigen-binding domain) of the fusion protein. For example, it is contemplated that a gene encoding a sialidase portion linked directly or indirectly (for example, via an amino acid containing linker) to an antibody portion can be created and expressed using conventional recombinant DNA technologies. For example, the amino terminus of a sialidase portion can be linked to the carboxy terminus of either the light or the heavy chain of an antibody portion. For example, for a Fab fragment, the amino terminus or carboxy terminus of the sialidase can be linked to the first constant domain of the heavy antibody chain (CHI). When a linker is employed, the linker may comprise hydrophilic amino acid residues, such as Gin, Ser, Gly, Glu, Pro, His and Arg. In certain embodiments, the linker is a peptide containing 1-25 amino acid residues, 1-20 amino acid residues, 2-15 amino acid residues, 3-10 amino acid residues, 3-7 amino acid residues, 4-25 amino acid residues, 4-20 amino acid residues, 4-15 amino acid residues, 4-10 amino acid residues, 5-25 amino acid residues, 5-20 amino acid residues, 5-15 amino acid residues, or 5-10 amino acid residues.

Exemplary linkers include glycine and serine-rich linkers, e.g., (GlyGlyPro) _n , or

(GlyGlyGlyGlySer) _n , where n is 1-5. In certain embodiments, the linker comprises, consists, or consists essentially of GGGGS (SEQ ID NO: 121). In certain embodiments, the linker comprises, consists, or consists essentially of GGGGSGGGGS (SEQ ID NO: 90). In certain embodiments, the linker comprises, consists, or consists essentially of EPKSS (SEQ ID NO: 91). Additional exemplary linker sequences are disclosed, e.g, in George et al. (2003) PROTEIN ENGINEERING 15:871-879, and U.S. Patent Nos. 5,482,858 and 5,525,491.

[00149] In certain embodiments, the fusion protein comprises the amino acid sequence of any one of SEQ ID NOs: 65-75, 78, 81-89, 95, 96, 98, 99, 101, 102, 104, 106, 108, 110, 112, 114, 122-124, 127, or 128, or an amino acid sequence that has at least 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to any one of SEQ ID NOs: 65-75, 78, 81-89, 95, 96, 98, 99, 101, 102, 104, 106, 108, 110, 112, 114, 122-124, 127, or 128. d. Antibody Conjugates

[00150] The invention further provides antibody conjugates containing one or more of the fusion proteins disclosed herein. As used herein, unless otherwise indicated, the term“antibody conjugate” is understood to refer to an antibody, or a functional fragment thereof, that comprises antigen-binding activity ( e.g ., anti-PD-Ll antigen-binding activity) and/or Fc receptor-binding activity, conjugated (e.g., covalently coupled) to an additional functional moiety. In certain embodiments, the antibody or functional antibody fragment is conjugated to a sialidase enzyme, e.g, a recombinant mutant human sialidase enzyme disclosed herein. In certain embodiments, an antibody conjugate comprises a single polypeptide chain. In certain embodiments, an antibody conjugate comprises two, three, four, or more polypeptide chains that are covalently or non-covalently associated together to produce a multimeric complex, e.g, a dimeric, trimeric or tetrameric complex. For example, an antibody conjugate may comprise a first polypeptide (fusion protein) comprising a recombinant mutant human sialidase enzyme and an

immunoglobulin heavy chain, and a second polypeptide comprising an immunoglobulin light chain, where, for example, the immunoglobulin heavy and light chains together define a single anti gen -binding site, e.g, an anti-PD-Ll anti gen -binding site.

[00151] In certain embodiments, the antibody conjugate can include a single sialidase. In other embodiments, the antibody conjugate can include more than one (e.g, two) sialidases. If more than one sialidase is included, the sialidases can be the same or different. In certain

embodiments, the antibody conjugate can include a single anti-PD-Ll antigen-binding site. In other embodiments, the antibody conjugate can include more than one (e.g, two) anti-PD-Ll antigen-binding sites. If two antigen-binding sites are used, they can be the same or different. In certain embodiments, the antibody conjugate comprises an immunoglobulin Fc fragment.

[00152] In certain embodiments, the antibody conjugate comprises one or two immunoglobulin heavy chains, or a functional fragment thereof. In certain embodiments, the antibody conjugate comprises one or two immunoglobulin light chains, or a functional fragment thereof. In certain embodiments, the antibody conjugate comprises a sialidase fused to the N- or C-terminus of an immunoglobulin heavy chain or an immunoglobulin light chain.

[00153] FIGURE 17 depicts exemplary antibody conjugate constructs containing one or more sialidase enzymes. For example, in FIGURE 17A, a first anti-PD-Ll antigen-binding site is depicted as 10, a second anti-PD-Ll antigen-binding site is depicted as 20, a sialidase is depicted as 30, and a Fab is depicted as 40. In each of the constructs depicted in FIGURES 17A-17I it is understood that the Fc may optionally be modified in some manner, e.g. using Knobs-into-Holes type technology, e.g, as depicted by 50 in FIGURE 17B. Throughout FIGURE 17 similar structures are depicted by similar schematic representations.

[00154] FIGURE 17A depicts antibody conjugate constructs comprising a first polypeptide comprising a first immunoglobulin light chain; a second polypeptide comprising a first immunoglobulin heavy chain; a third polypeptide comprising a second immunoglobulin heavy chain; and a fourth polypeptide comprising a second immunoglobulin light chain. The first and second polypeptides can be covalently linked together, the third and fourth polypeptides can be covalently linked together, and the second and third polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. In certain embodiments, the first polypeptide and the second polypeptide together define a first anti-PD-Ll antigen-binding site as depicted as 10, and the third polypeptide and the fourth polypeptide together define a second anti-PD-Ll antigen-binding site as depicted as 20. A sialidase enzyme as depicted as 30 can be conjugated to the N- or C-terminus of the first and second immunoglobulin light chain or the first and second immunoglobulin heavy chain.

[00155] FIGURE 17B depicts antibody conjugate constructs comprising a first polypeptide comprising a first immunoglobulin light chain; a second polypeptide comprising a first immunoglobulin heavy chain; a third polypeptide comprising a second immunoglobulin heavy chain; and a fourth polypeptide comprising a second immunoglobulin light chain. The first and second polypeptides can be covalently linked together, the third and fourth polypeptides can be covalently linked together, and the second and third polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. In certain embodiments, the first polypeptide and the second polypeptide together define a first anti-PD-Ll antigen-binding site, and the third polypeptide and the fourth polypeptide together define a second anti-PD-Ll antigen-binding site. A sialidase enzyme can be conjugated to the N- or C-terminus of the first immunoglobulin light chain or the first immunoglobulin heavy chain.

[00156] FIGURE 17C depicts antibody conjugate constructs comprising a first polypeptide comprising an immunoglobulin light chain; a second polypeptide comprising an

immunoglobulin heavy chain; and a third polypeptide comprising an immunoglobulin Fc domain. The first and second polypeptides can be covalently linked together and the second and third polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. In certain embodiments, the first polypeptide and the second polypeptide together define an anti-PD-Ll antigen-binding site. A sialidase enzyme can be conjugated to the N- or C- terminus of the first immunoglobulin light chain or the first immunoglobulin heavy chain. [00157] FIGURE 17D depicts antibody conjugate constructs comprising a first polypeptide comprising an immunoglobulin light chain; a second polypeptide comprising an

immunoglobulin heavy chain; and a third polypeptide comprising an immunoglobulin Fc domain and a first sialidase enzyme. The first and second polypeptides can be covalently linked together and the second and third polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. The third polypeptide comprises the sialidase and the immunoglobulin Fc domain in an N- to C-terminal orientation. In certain embodiments, the first polypeptide and the second polypeptide together define an anti-PD-Ll antigen-binding site. An optional second sialidase enzyme can be conjugated to the N- or C-terminus of the first immunoglobulin light chain or the first immunoglobulin heavy chain.

[00158] FIGURE 17E depicts antibody conjugate constructs comprising a first polypeptide comprising an immunoglobulin light chain; a second polypeptide comprising an

immunoglobulin heavy chain; and a third polypeptide comprising an immunoglobulin Fc domain and a first sialidase enzyme. The first and second polypeptides can be covalently linked together and the second and third polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. The third polypeptide comprises the immunoglobulin Fc domain and the sialidase in an N- to C-terminal orientation. In certain embodiments, the first polypeptide and the second polypeptide together define an anti-PD-Ll antigen-binding site. An optional second sialidase enzyme can be conjugated to the N- or C-terminus of the first immunoglobulin light chain or the first immunoglobulin heavy chain.

[00159] FIGURE 17F depicts antibody conjugate constructs comprising a first polypeptide comprising a first immunoglobulin Fc domain, and a second polypeptide comprising a second immunoglobulin Fc domain. The first and second polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. A sialidase enzyme can be conjugated to the N- or C-terminus of the first immunoglobulin Fc domain or to the N- or C-terminus of the second immunoglobulin Fc domain. An optional second sialidase enzyme can be conjugated to the N- or C-terminus of the first immunoglobulin Fc domain or to the N- or C-terminus of the second immunoglobulin Fc domain.

[00160] FIGURE 17G depicts antibody conjugate constructs comprising a first polypeptide comprising an immunoglobulin light chain; and a second polypeptide comprising an

immunoglobulin heavy chain variable region. The first and second polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. In certain

embodiments, the first polypeptide and the second polypeptide together define an anti-PD-Ll antigen-binding site. The sialidase enzyme can be conjugated to the N- or C-terminus of the immunoglobulin light chain or the immunoglobulin heavy chain variable region.

[00161] FIGURE 17H depicts antibody conjugate constructs comprising a first polypeptide comprising a first immunoglobulin Fc domain, and a second polypeptide comprising a second immunoglobulin Fc domain. The first and second polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. A sialidase enzyme can be conjugated to the N-terminus of the first immunoglobulin Fc domain or the second immunoglobulin Fc domain. An optional second sialidase enzyme can be conjugated to the N-terminus of the second immunoglobulin Fc domain or the first immunoglobulin Fc domain, respectively. A single chain variable fragment (scFv) can be conjugated to the C-terminus of the first immunoglobulin Fc domain or the second immunoglobulin Fc domain. An optional second single chain variable fragment (scFv) can be conjugated to the C-terminus of the first immunoglobulin Fc domain or the second immunoglobulin Fc domain, respectively.

[00162] FIGURE 171 depicts antibody conjugate constructs similar to those depicted in

FIGURE 17H except that each scFv is replaced with an immunoglobulin antigen binding fragment, e.g ., an Fab. For example, FIGURE 171 depicts antibody conjugate constructs comprising a first polypeptide comprising a first immunoglobulin Fc domain, and a second polypeptide comprising a second immunoglobulin Fc domain. The first and second polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. A sialidase enzyme can be conjugated to the N-terminus of the first immunoglobulin Fc domain or the second immunoglobulin Fc domain. An optional second sialidase enzyme can be conjugated to the N-terminus of the second immunoglobulin Fc domain or the first immunoglobulin Fc domain, respectively. An antibody fragment (Fab) can be conjugated or fused to the C-terminus of the first immunoglobulin Fc domain or the second immunoglobulin Fc domain. An optional second antibody fragment (Fab) can be conjugated or fused to the C-terminus of the second immunoglobulin Fc domain or the first immunoglobulin Fc domain, respectively. In the case of a fusion, the C terminus of the Fc domain is linked (either by a bond or an amino acid linker) to a first polypeptide chain defining an anti-PD-Ll immunoglobulin antigen binding fragment. In the case of antibodies that have an antigen binding site defined by a single variable region, then this may be sufficient to impart binding affinity to a target antigen, e.g. , PD-L1. In other instances, e.g. , in the case of a human antibody, the first polypeptide chain defining an immunoglobulin antigen binding fragment can be conjugated (e.g, covalently conjugated, e.g, via a disulfide bond) to a second polypeptide chain defining an immunoglobulin antigen binding fragment, there the two antigen binding fragments together define an antigen binding site for binding the target antigen, e.g ., PD-L1.

[00163] FIGURE 18 depicts additional antibody conjugate constructs. For example,

FIGURE 18 depicts an antibody conjugate construct comprising a first polypeptide comprising an immunoglobulin light chain; a second polypeptide comprising an immunoglobulin heavy chain and an scFv; and a third polypeptide comprising an immunoglobulin Fc domain and a first sialidase enzyme. The first and second polypeptides can be covalently linked together and the second and third polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. The second polypeptide comprises the heavy chain and the scFv in an N- to C- terminal orientation. The third polypeptide comprises the sialidase and the immunoglobulin Fc domain in an N- to C-terminal orientation. In certain embodiments, the first polypeptide and the second polypeptide together define a first antigen-binding site. In certain embodiments, the scFv defines a second antigen-binding site. FIGURE 18 depicts an additional antibody construct comprising a first polypeptide comprising an immunoglobulin light chain; a second polypeptide comprising an immunoglobulin heavy chain; and a third polypeptide comprising an immunoglobulin Fc domain and a first sialidase enzyme, wherein a Fab fragment is conjugated to the N-terminus of the immunoglobulin heavy chain. The first and second polypeptides can be covalently linked together and the second and third polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. The third polypeptide comprises the sialidase and the immunoglobulin Fc domain in an N- to C-terminal orientation. In certain embodiments, the first polypeptide and the second polypeptide together define a first antigen binding site. In certain embodiments, the Fab fragment defines a second antigen-binding site.

In each of the constructs depicted in FIGURE 18 it is understood that an scFv, when present, may be replaced with a Fab fragment, or a Fab fragment, when present, may be replaced with an scFv. In each of the constructs depicted in FIGURE 18, it is understood that the Fc may optionally be modified in some manner.

[00164] In certain embodiments, the antibody conjugate comprises a first polypeptide comprising a first immunoglobulin light chain; a second polypeptide comprising a first immunoglobulin heavy chain and a first sialidase; a third polypeptide comprising a second immunoglobulin heavy chain and a second sialidase; and a fourth polypeptide comprising a second immunoglobulin light chain. An example of this embodiment is shown in FIGURE 19A. The first and second polypeptides can be covalently linked together, the third and fourth polypeptides can be covalently linked together, and the second and third polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. In certain embodiments, the first polypeptide and the second polypeptide together define a first anti-PDL-1 antigen-binding site, and the third polypeptide and the fourth polypeptide together define a second anti-PD-Ll antigen-binding site. In certain embodiments, the second and third polypeptides comprise the first and second immunoglobulin heavy chain and the first and second sialidase, respectively, in an N- to C-terminal orientation. In certain embodiments, the second and third polypeptides comprise the first and second sialidase and the first and second immunoglobulin heavy chain, respectively, in an N- to C-terminal orientation.

[00165] In certain embodiments, the antibody conjugate comprises a first polypeptide comprising an immunoglobulin light chain; a second polypeptide comprising an

immunoglobulin heavy chain; and a third polypeptide comprising an immunoglobulin Fc domain and a sialidase. An example of this embodiment is shown in FIGURE 19B. The first and second polypeptides can be covalently linked together and the second and third polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. In certain embodiments, the first polypeptide and the second polypeptide together define an anti-PD-Ll antigen-binding site. In certain embodiments, the third polypeptide comprises the sialidase and the immunoglobulin Fc domain in an N- to C-terminal orientation, or the immunoglobulin Fc domain and the sialidase in an N- to C-terminal orientation.

[00166] In certain embodiments, the first polypeptide comprises the amino acid sequence of SEQ ID NO: 65, or an amino acid sequence that has at least 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO: 65. In certain embodiments, the second polypeptide comprises the amino acid sequence of any one of SEQ ID NOs: 66, 104, or 124, or an amino acid sequence that has at least 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to any one of SEQ ID NOs: 66, 104, or 124. In certain embodiments, the third polypeptide comprises the amino acid sequence of any one of SEQ ID NOs: 67-73, 78, 81-87, 95, 96, 98, 99, 101, 102, 106, 108, 112, 122, 123, 127, or 128, or an amino acid sequence that has at least 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to any one of SEQ ID NOs: 67-73, 78, 81-87, 95, 96, 98, 99, 101, 102, 106, 108, 112, 122, 123, 127, or 128.

[00167] In certain embodiments, the third polypeptide comprises the amino acid sequence of

X ₁ X ₂ SX ₃ X ₄ X ₅ LQX ₆ ESVFQSGAHAYRI PALLYLPGQQSLLAFAEQRASX ₇ X ₈ DEHAEL IVX ₉ RRGD

YDAX10THQVQWX11AQEWAQAX12LDGHRSMNPCPLYDX13QTGTLFLFFIAI PX14X15VTEX16Q

QLQTRANVTRLX17X18VTS TDHGRTWS S PRDLTDAAI GPX19YREWS T FAVGPGHX20LQLHDRX21

RSLWPAYAYRKLHPX ₂₂ QRP I PSAFX ₂₃ FLSHDHGRTWARGHFVAQDTX ₂₄ ECQVAEVETGEQRV

VTLNARSHLRARVQAQSX ₂₅ NX ₂₆ GLDFQX ₂₇ SQLVKKLVEPPPX ₂₈ GX ₂₉ QGSVI S FPS PRSGPGS P

AQX ₃₀ LLYTHPTHX ₃₁ X ₃₂ QRADLGAYLNPRPPAPEAWSEPX ₃₃ LLAKGSX ₃₄ AYSDLQSMGTGPDGS PLFGX ₃₅ LYEANDYEE IX ₃₆ FX ₃₇ MFTLKQAFPAEYLPQGGGGSGGGGSDKTHTCPPCPAPELLGG

PSVFLFPPKPKDTLMI SRTPEVTCVWDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNS TYR

WSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKT I SKAKGQPREPQVYTLPPSREEMTKNQVSL

TCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGS FFLTSKLTVDKSRWQQGNVFSCSVMH

EALHNHYTQKSLSLS PGK

(SEQ ID NO: 75), wherein Xi is Ala, Arg, Asn, Asp, Gin, Glu, Gly, His, Leu, Lys, Met, Phe, Thr, Val, or not present, X ₂ is Ala or Lys, X ₃ is Asn or Leu, X ₄ is Pro or His, X ₅ is Phe, Trp, Tyr or Val, X ₍ , is Lys or Asp, X ₇ is Lys, Arg, or Glu. Xx is Lys, Ala, Arg, or Glu, X ₉ is Leu or Met,

X ₁₀ is Pro, Asn, Asp, His, Glu, Gly, Ser or Thr, Xu is Gin or His, X ₁₂ is Arg or Lys, X ₁₃ is Ala, Glu or Lys, X ₁₄ is Gly or Asp, X ₁₅ is Gin or His, X½ is Gin, Arg, or Lys, X ₁₇ is Ala, Cys, lie, Ser, Val, or Leu, Xis is Gin or Leu, X ₁₉ is Ala or Val, X ₂₀ is Cys or Gly, X ₂₁ is Ala or Gly, X ₂₂ is Arg, lie, or Lys, X ₂₃ is Ala, Cys, Leu, or Val, X ₂₄ is Leu, Ala, or Val, X ₂₅ is Thr or Ala, X ₂₆ is Asp or Gly, X ₂₇ is Glu or Lys, X ₂₈ is Gin, Ala, His, Phe, or Pro, X ₂₉ is Cys or Val, X ₃₀ is Trp or Arg, X ₃₁ is Ser or Arg, X ₃₂ is Trp or Lys, X ₃₃ is Lys or Val, X ₃₄ is Ala, Cys, Ser, or Val, X ₃₅ is Cys, Leu, or Val, X _{36 IS} Val or Arg, and X _{37 IS} Leu, Gin, His, He, Lys, or Ser, and the sialidase comprises at least one mutation relative to wild-type human Neu2 (SEQ ID NO: 1).

[00168] In certain embodiments, the third polypeptide comprises the amino acid sequence of

X1ASLPX2LQX3ESVFQSGAHAYRI PALLYLPGQQSLLAFAEQRASKKDEHAEL IVLRRGDYDAX4

THQVQWQAQEWAQARLDGHRSMNPCPLYDX ₅ QTGTLFLFFIAI PGQVTEQQQLQTRANVTRLCQ

VT S TDHGRTWS S PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPXeQRP

I PSAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQS TNDGLD

FQESQLVKKLVEPPPX ₇ GCQGSVI S FPS PRSGPGS PAQWLLYTHPTHX ₈ X ₉ QRADLGAYLNPRPP

APEAWSEPVLLAKGSX ₁₀ AYSDLQSMGTGPDGS PLFGCLYEANDYEE IX ₁₁ FX ₁₂ MFTLKQAFPAE

YLPQGGGGSGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMI SRTPEVTCWVDVSHED

PEVKFNWYVDGVEVHNAKTKPREEQYNS TYRWSVLTVLHQDWLNGKEYKCKVSNKALPAP IEK

T I SKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPP VL

DSDGS FFLTSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLS PGK

(SEQ ID NO: 74), wherein Xi is Ala, Arg, Asn, Asp, Gin, Glu, Gly, His, Leu, Lys, Met, Phe,

Thr, Val, or not present, X ₂ is Phe, Trp, Tyr or Val, X ₃ is Lys or Asp, X ₄ is Pro, Asn, Asp, His,

Glu, Gly, Ser or Thr, X ₅ is Ala, Glu, or Lys, C _ό is Arg, He, or Lys, X ₇ is Gin, Ala, His, Phe, or

Pro, X ₈ is Ser or Arg, X ₉ is Trp or Lys, X ₁₀ is Ala, Cys, Ser, or Val, Xu is Val or Arg, and X ₁₂ is

Leu, Gin, His, He, Lys, or Ser, and the sialidase comprises at least one mutation relative to wild- type human Neu2 (SEQ ID NO: 1). In certain embodiments, Xi is Ala, Asp, Met, or not present,

X ₂ is Tyr or Val, X ₃ is Lys or Asp, X ₄ is Pro, Asn, Gly, Ser or Thr, X ₅ is Ala or Glu, C _ό is He or

Lys, X ₇ is Gin or Ala, Xs is Ser or Arg, X ₉ is Trp or Lys, X ₁₀ is Ala or Cys, Xu is Val or Arg, and

X12 is Leu or He.

[00169] In certain embodiments, the third polypeptide comprises the amino acid sequence of

X ₁ X ₂ SX ₃ X ₄ X ₅ LQX ₆ ESVFQSGAHAYRI PALLYLPGQQSLLAFAEQRASX ₇ X ₈ DEHAEL IVX ₉ RRGD

YDAX10THQVQWX11AQEWAQAX12LDGHRSMNPCPLYDX13QTGTLFLFFIAI PX14X15VTEX16Q QLQTRANVTRLX17X18VTS TDHGRTWS S PRDLTDAAI GPX19YREWS T FAVGPGHX20LQLHDRX21

RSLWPAYAYRKLHPX ₂₂ QRP I PSAFX ₂₃ FLSHDHGRTWARGHFVAQDTX ₂₄ ECQVAEVETGEQRV

VTLNARSHLRARVQAQSX ₂₅ NX ₂₆ GLDFQX ₂₇ SQLVKKLVEPPPX ₂₈ GX ₂₉ QGSVI S FPS PRSGPGS P

AQX ₃₀ LLYTHPTHX ₃₁ X ₃₂ QRADLGAYLNPRPPAPEAWSEPX ₃₃ LLAKGSX ₃₄ AYSDLQSMGTGPDGS

PLFGX ₃₅ LYEANDYEE IX ₃₆ FX ₃₇ MFTLKQAFPAEYLPQX ₃₈ DKTHTCPPCPAPELLGGPSVFLFPP

KPKDTLMI SRTPEVTCVWDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNS TYRWSVLTVL

HQDWLNGKEYKCKVSNKALPAP IEKT I SKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFY

PSDIAVEWESNGQPENNYKTTPPVLDSDGS FFLTSKLTVDKSRWQQGNVFSCSVMHEALHNHYT

QKSLSLS PGK

(SEQ ID NO: 89), wherein Xi is Ala, Arg, Asn, Asp, Gin, Glu, Gly, His, Leu, Lys, Met, Phe, Thr, Val, or not present, X ₂ is Ala or Lys, X ₃ is Asn or Leu, X ₄ is Pro or His, X ₅ is Phe, Trp, Tyr or Val, X ₍ , is Lys or Asp, X ₇ is Lys, Arg, or Glu. Xx is Lys, Ala, Arg, or Glu, X ₉ is Leu or Met,

X ₁₀ is Pro, Asn, Asp, His, Glu, Gly, Ser or Thr, Xu is Gin or His, X ₁₂ is Arg or Lys, X ₁₃ is Ala, Glu or Lys, X ₁₄ is Gly or Asp, X ₁₅ is Gin or His, X½ is Gin, Arg, or Lys, X ₁₇ is Ala, Cys, lie, Ser, Val, or Leu, Xis is Gin or Leu, X ₁₉ is Ala or Val, X ₂₀ is Cys or Gly, X ₂₁ is Ala or Gly, X ₂₂ is Arg, lie, or Lys, X ₂₃ is Ala, Cys, Leu, or Val, X ₂₄ is Leu, Ala, or Val, X ₂₅ is Thr or Ala, X ₂₆ is Asp or Gly, X ₂₇ is Glu or Lys, X ₂₈ is Gin, Ala, His, Phe, or Pro, X ₂₉ is Cys or Val, X ₃₀ is Trp or Arg, X ₃₁ is Ser or Arg, X ₃₂ is Trp or Lys, X ₃₃ is Lys or Val, X ₃₄ is Ala, Cys, Ser, or Val, X ₃₅ is Cys, Leu, or Val, X ₃₆ is Val or Arg, X ₃₇ is Leu, Gin, His, He, Lys, or Ser, and X ₃₈ is GGGGSGGGGS (SEQ ID NO: 90) or EPKSS (SEQ ID NO: 91), and the sialidase comprises at least one mutation relative to wild-type human Neu2 (SEQ ID NO: 1).

[00170] In certain embodiments, the third polypeptide comprises the amino acid sequence of

X1ASLPX2LQX3ESVFQSGAHAYRI PALLYLPGQQSLLAFAEQRASKKDEHAEL IVLRRGDYDAX4

THQVQWQAQEWAQARLDGHRSMNPCPLYDX ₅ QTGTLFLFFIAI PGQVTEQQQLQTRANVTRLCQ

VT S TDHGRTWS S PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPXeQRP

I PSAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQS TNDGLD

FQESQLVKKLVEPPPX ₇ GCQGSVI S FPS PRSGPGS PAQWLLYTHPTHX ₈ X ₉ QRADLGAYLNPRPP

APEAWSEPVLLAKGSX ₁₀ AYSDLQSMGTGPDGS PLFGCLYEANDYEE IX ₁₁ FX ₁₂ MFTLKQAFPAE

YLPQGGGGSGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMI SRTPEVTCWVDVSHED

PEVKFNWYVDGVEVHNAKTKPREEQYNS TYRWSVLTVLHQDWLNGKEYKCKVSNKALPAP IEK

T I SKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPP VL

DSDGS FFLTSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLS PGK

(SEQ ID NO: 88), wherein Xi is Ala, Arg, Asn, Asp, Gin, Glu, Gly, His, Leu, Lys, Met, Phe,

Thr, Val, or not present, X ₂ is Phe, Trp, Tyr or Val, X ₃ is Lys or Asp, X ₄ is Pro, Asn, Asp, His,

Glu, Gly, Ser or Thr, X ₅ is Ala, Glu, or Lys, C _ό is Arg, He, or Lys, X ₇ is Gin, Ala, His, Phe, or

Pro, X ₈ is Ser or Arg, X ₉ is Trp or Lys, X ₁₀ is Ala, Cys, Ser, or Val, Xu is Val or Arg, X ₁₂ is Leu,

Gin, His, He, Lys, or Ser, and X ₁₃ is GGGGSGGGGS (SEQ ID NO: 90) or EPKSS (SEQ ID NO:

91), and the sialidase comprises at least one mutation relative to wild-type human Neu2 (SEQ ID

NO: 1). In certain embodiments, Xi is Ala, Asp, Met, or not present, X ₂ is Tyr or Val, X ₃ is Lys or Asp, X4 is Pro, Asn, Gly, Ser or Thr, X5 is Ala or Glu, Xe is He or Lys, X7 is Gin or Ala, Xs is Ser or Arg, X9 is Trp or Lys, X10 is Ala or Cys, Xu is Val or Arg, and X12 is Leu or He.

[00171] In certain embodiments, the third polypeptide comprises the amino acid sequence of

X ₁ X ₂ SX ₃ X ₄ X ₅ LQX ₆ ESVFQSGAHAYRI PALLYLPGQQSLLAFAEQRASX ₇ X ₈ DEHAEL IVX ₉ RRGD

YDAX10THQVQWX11AQEWAQAX12LX13GHRSMNPCPLYDX14QTGTLFLFFIAI PX15X16VTEX17

QQLQTRANVTRLX18X19VTS TDHGRTWS S PRDLTDAAI GPX20YREWS T FAVGPGHX21LQLHDX22

X ₂₃ RSLWPAYAYRKLHPX ₂₄ X ₂₅ X ₂₆ PI PSAFX ₂₇ FLSHDHGRTWARGHFVX ₂₈ QDTX ₂₉ ECQVAEVX

₃₀ TGEQRWTLNARSX ₃₁ X ₃₂ X ₃₃ X ₃₄ RX ₃₅ QAQSX ₃₆ NX ₃₇ GLDFQX ₃₈ X ₃₉ QX ₄₀ VKKL

X ₄₁ EPPPX ₄₂ GX ₄₃ QGSVI S FPS PRSGPGS PAQX ₄₄ LLYTHPTHX ₄₅ X ₄₆ QRADLGAYLNPRPPAPEA

WSEPX ₄₇ LLAKGSX ₄₈ AYSDLQSMGTGPDGS PLFGX ₄₉ LYEANDYEE IX ₅₀ FX ₅₁ MFTLKQAFPAEYL

PQX ₅₂ DKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMI SRTPEVTCWVDVSHEDPEVKFNWYVD

GVEVHNAKTKPREEQYNS TYRWSVLTVLHQDWLNGKEYKCKVSNKALPAP IEKT I SKAKGQPR

EPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSD GS FFLTS

KLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLS PGK

(SEQ ID NO: 117), wherein Xi is Ala, Arg, Asn, Asp, Gin, Glu, Gly, His, Leu, Lys, Met, Phe, Thr, Val, or not present, X2 is Ala or Lys, X3 is Asn or Leu, X4 is Pro or His, X5 is Phe, Trp, Tyr or Val, X ₍ , is Lys or Asp, X7 is Lys, Arg, or Glu, Xx is Lys, Ala, Arg, or Glu, X9 is Leu or Met,

X ₁₀ is Pro, Asn, Asp, His, Glu, Gly, Ser or Thr, Xu is Gin or His, X ₁₂ is Arg or Lys, X ₁₃ is Asp or Pro, Xi ₄ is Ala, Glu or Lys, X ₁₅ is Gly or Asp, X½ is Gin or His, X ₁₇ is Gin, Arg, or Lys, Xis is Ala, Cys, lie, Ser, Val, or Leu, X ₁₉ is Gin, Leu, Glu, Phe, His, He, Leu, or Tyr, X ₂₀ is Ala or Val, X ₂₁ is Cys or Gly, X ₂₂ is Arg or Pro, X ₂₃ is Ala or Gly, X ₂₄ is Arg, He, or Lys, X ₂₅ is Gin or Pro, X ₂₆ is Arg or Pro, X ₂₇ is Ala, Cys, Leu, or Val, X ₂₈ is Ala, Cys, Asn, Ser, or Thr, X ₂₉ is Leu, Ala, or Val, X ₃₀ is Glu or Pro, X ₃₁ is His or Pro, X ₃₂ is Leu, Asp, Asn, or Tyr, X ₃₃ is Arg, Ala, Asp, Leu, Gin, or Tyr, X ₃₄ is Ala, Cys, Phe, Gly, His, He, Lys, Leu, Met, Asn, Gin, Arg, Ser, Val, Trp, or Tyr, X ₃₅ is Val, He, or Lys, X ₃₆ is Thr or Ala, X ₃₇ is Asp or Gly, X ₃₈ is Glu, Lys, or Pro, X ₃₉ is Ser or Cys, X ₄₀ is Leu, Asp, Phe, Gin, or Thr, X ₄₁ is Val or Phe, X ₄₂ is Gin, Ala, His, Phe, Pro, Ser, or Thr, X ₄₃ is Cys or Val, X ₄₄ is Trp or Arg, X ₄₅ is Ser, Arg, Ala, Asp, Glu, Phe, Gly, His,

He, Lys, Leu, Met, Asn, Pro, Gin, Thr, Val, Trp, or Tyr, X46 IS Trp, Lys, Ala, Asp, Glu, Phe, Gly, His, He, Lys, Leu, Met, Asn, Pro, Gin, Arg, Ser, Thr, Val, or Tyr, X47 IS Lys or Val, X48 IS Ala, Cys, Ser, or Val, X49 is Cys, Leu, or Val, X50 is Val or Arg, X51 is Leu, Gin, His, He, Lys, or Ser, X52 is GGGGS (SEQ ID NO: 121), GGGGSGGGGS (SEQ ID NO: 90), or EPKSS (SEQ ID NO: 91), and the sialidase comprises at least one mutation relative to wild-type human Neu2 (SEQ ID NO: 1).

[00172] In certain embodiments, the third polypeptide comprises the amino acid sequence of

X1ASLPX2LQX3ESVFQSGAHAYRI PALLYLPGQQSLLAFAEQRASKKDEHAEL IVLRRGDYDAX4 THQVQWQAQEWAQARLDGHRSMNPCPLYDX ₅ QTGTLFLFFIAI PGQVTEQQQLQTRANVTRLCX ₆ VT S TDHGRTWS S PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPX ₇ QR P I PSAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRXsRVQAQS TNDGL DFQESQLVKKLVEPPPX ₉ GCQGSVI S FPS PRSGPGS PAQWLLYTHPTHX ₁₀ X ₁₁ QRADLGAYLNPR PPAPEAWSEPVLLAKGSX ₁₂ AYSDLQSMGTGPDGS PLFGCLYEANDYEE IX ₁₃ FX ₁₄ MFTLKQAFP

AEYLPQX ₁₅ DKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMI SRTPEVTCWVDVSHEDPEVKFN

WYVDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEK TISKAK

GQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPV LDSDGSF

FLTSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

(SEQ ID NO: 116), wherein Xi is Ala, Arg, Asn, Asp, Gin, Glu, Gly, His, Leu, Lys, Met, Phe, Thr, Val, or not present, X2 is Phe, Trp, Tyr or Val, X3 is Lys or Asp, X4 is Pro, Asn, Asp, His, Glu, Gly, Ser or Thr, X5 is Ala, Glu, or Lys, C _ό is Gin, Leu, Glu, Phe, His, lie, Leu, or Tyr, X7 is Arg, lie, or Lys, Xs is Ala, Cys, Phe, Gly, His, He, Lys, Leu, Met, Asn, Gin, Arg, Ser, Val, Trp, or Tyr, X9 IS Gin, Ala, His, Phe, Pro, Ser, or Thr, Xio is Ser, Arg, Ala, Asp, Glu, Phe, Gly, His, He, Lys, Leu, Met, Asn, Pro, Gin, Thr, Val, Trp, or Tyr, Xu is Trp, Lys, Ala, Asp, Glu, Phe, Gly, His, He, Lys, Leu, Met, Asn, Pro, Gin, Arg, Ser, Thr, Val, or Tyr, Xo is Ala, Cys, Ser, or Val,

Xi ₃ is Val or Arg, X14 is Leu, Gin, His, He, Lys, or Ser, X15 is GGGGS (SEQ ID NO: 121), GGGGSGGGGS (SEQ ID NO: 90), or EPKSS (SEQ ID NO: 91), and the sialidase comprises at least one mutation relative to wild-type human Neu2 (SEQ ID NO: 1). In certain embodiments, Xi is Ala, Asp, Met, or not present, X2 is Tyr or Val, X3 is Lys or Asp, X4 is Pro, Asn, Gly, Ser or Thr, X5 is Ala or Glu, Xr, is Gin or Tyr, X7 is He or Lys, Xx is Ala or Thr, X9 is Gin, Ala, or Thr, X10 is Ser, Arg, or Ala, Xu is Trp, Lys, or Arg, X12 is Ala or Cys, X13 is Val or Arg, and X14 is Leu or He.

[00173] In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 67. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 68. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 69. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 70. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 71. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 72. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 73. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 78. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 81. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 82. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 83. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 84. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 85. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 86. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 87. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 95. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 96. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 98. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 99. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 101. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 102. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 106. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 112. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 127. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 66, and the third polypeptide comprises SEQ ID NO: 128. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 104, and the third polypeptide comprises SEQ ID NO: 108. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 124, and the third polypeptide comprises SEQ ID NO: 122. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 124, and the third polypeptide comprises SEQ ID NO: 123.

[00174] In certain embodiments, the antibody conjugate comprises a first polypeptide comprising a first sialidase, a first immunoglobulin Fc domain, and a first single chain variable fragment (scFv) (it is also understood that the scFv may be replaced by a first polypeptide chain of an immunoglobulin antigen binding fragment, e.g ., Fab fragment); and a second polypeptide comprising a second sialidase, a second immunoglobulin Fc domain, and a second single chain variable fragment (scFv) (it is also understood that the scFv may be replaced by a second polypeptide chain of an immunoglobulin antigen binding fragment, e.g. , Fab fragment). An example of this embodiment is shown in FIGURE 19C. The first and second polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. In certain embodiments, the first scFv defines a first anti-PD-Ll antigen-binding site, and the second scFv defines a second anti-PD-Ll antigen-binding site. In certain embodiments, the first polypeptide comprises the first sialidase, the first immunoglobulin Fc domain, and the first scFv in an N- to C -terminal orientation. In certain embodiments, the first polypeptide comprises the first scFv, the first immunoglobulin Fc domain, and the first sialidase in an N- to C-terminal orientation. In certain embodiments, the second polypeptide comprises the second sialidase, the second immunoglobulin Fc domain, and the second scFv in an N- to C-terminal orientation. In certain embodiments, the second polypeptide comprises the second scFv, the second immunoglobulin Fc domain, and the second sialidase in an N- to C-terminal orientation.

[00175] In certain embodiments, the first polypeptide comprises the amino acid sequence of SEQ ID NO: 114, or an amino acid sequence that has at least 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO: 114. In certain embodiments, the second polypeptide comprises the amino acid sequence of SEQ ID NO: 114, or an amino acid sequence that has at least 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO: 114. In certain embodiments, the first and second polypeptide comprise SEQ ID NO: 114.

[00176] In certain embodiments, the antibody conjugate comprises: a first polypeptide comprising an immunoglobulin light chain; a second polypeptide comprising an

immunoglobulin heavy chain and a single chain variable fragment (scFv) (it is also understood that the scFv may be replaced by a first polypeptide chain of an immunoglobulin antigen binding fragment, e.g. , Fab fragment); and a third polypeptide comprising an immunoglobulin Fc domain and a sialidase. An example of this embodiment is shown in FIGURE 19D. The first and second polypeptides can be covalently linked together and the second and third polypeptides can be covalently linked together. The covalent linkages can be disulfide bonds. In certain embodiments, the first polypeptide and the second polypeptide together define a first anti-PD-Ll antigen-binding site (i.e., the immunoglobulin light chain and immunoglobulin heavy chain together define a first anti-PD-Ll antigen-binding site). In certain embodiments, the scFv defines a second anti-PD-Ll antigen-binding site. In certain embodiments, the second polypeptide comprises the immunoglobulin heavy chain and the scFv in an N- to C-terminal orientation, or the scFv and the immunoglobulin heavy chain in an N- to C-terminal orientation. In certain embodiments, the third polypeptide comprises the sialidase and the immunoglobulin Fc domain in an N- to C-terminal orientation, or the sialidase and the immunoglobulin Fc domain in an N- to C-terminal orientation.

[00177] In certain embodiments, the first polypeptide comprises the amino acid sequence of SEQ ID NO: 65, or an amino acid sequence that has at least 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO: 65. In certain embodiments, the second polypeptide comprises the amino acid sequence of SEQ ID NO: 110, or an amino acid sequence that has at least 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO: 110. In certain embodiments, the third polypeptide comprises the amino acid sequence of any one of SEQ ID NOs: 78 or 106, or an amino acid sequence that has at least 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to any one of SEQ ID NOs: 78 or 106. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 110, and the third polypeptide comprises SEQ ID NO: 78. In certain embodiments, the first polypeptide comprises SEQ ID NO: 65, the second polypeptide comprises SEQ ID NO: 110, and the third polypeptide comprises SEQ ID NO: 106.

[00178] In certain embodiments, the antibody conjugate has a molecular weight from about 135 kDa to about 165 kDa, e.g., about 140 kDa. In other embodiments, the antibody conjugate has a molecular weight from about 215 kDa to about 245 kDa, e.g, about 230 kDa.

[00179] In certain embodiments, the antibody conjugate comprises two polypeptides that each comprise an immunoglobulin Fc domain, and the first polypeptide has either a“knob” mutation, e.g, T366Y, or a“hole” mutation, e.g, Y407T, for heterodimerization with the second polypeptide, and the second polypeptide has either a respective“knob” mutation, e.g, T366Y, or a“hole” mutation, e.g., Y407T, for heterodimerization with the first polypeptide (residue numbers according to EU numbering, Kabat, E.A., et al. (1991) supra). For example, in certain embodiments, the antibody comprises two polypeptides that each comprise an immunoglobulin Fc domain derived from human IgGl Fc domain, and the first polypeptide comprises a Y407T mutation (e.g, the first polypeptide comprises SEQ ID NO: 32 or SEQ ID NO: 92), and the second polypeptide comprises a T366Y mutation (e.g, the second polypeptide comprises SEQ ID NO: 33 or SEQ ID NO: 93).

[00180] As used herein, the term“multispecific antibody” is understood to mean an antibody that specifically binds to at least two different antigens, i.e., an antibody that comprises at least two antigen-binding sites that bind to at least two different antigens. As used herein, the term “bispecific antibody” is understood to mean an antibody that specifically binds to two different antigens, i.e., an antibody that comprises two antigen-binding sites each of which bind to separate and distinct antigens. In other words, a first binding site binds a first antigen and a second binding site binds a second, different antigen. A multispecific or bispecific antibody may, for example, be a human or humanized antibody, and/or be a full length antibody or an antibody fragment (e.g, a F(ab’) ₂ bispecific antibody).

[00181] The present invention encompasses antibody conjugates comprising antibody fragments, which may be generated by traditional means, such as enzymatic digestion, or by recombinant techniques. For a review of certain antibody fragments, see Hudson et al. (2003) supra.

[00182] In certain embodiments, the antibody conjugate or fusion protein can be covalently or non-covalently associated with a biological modifier, wherein the biological modifier can be used to enhance the solubility of the antibody, increase binding specificity, decrease

immunogenicity or toxicity or modify the pharmacokinetic profile of the antibody. For example, the biological modifier can be used to increase the molecular weight of the antibody to increase its circulating half-life.

[00183] It is contemplated that the antibody conjugate or fusion protein may be covalently bound to one or more (for example, 2, 3, 4, 5, 6, 8, 9, 10 or more) biological modifiers that may comprise linear or branched polymers. Exemplary biological modifiers may include, for example, a variety of polymers, such as those described in U.S. Patent No. 7,842,789.

Particularly useful are polyalkylene ethers such as polyethylene glycol (PEG) and derivatives thereof (for example, alkoxy polyethylene glycol, for example, methoxypolyethylene glycol, ethoxypolyethylene glycol and the like); block copolymers of polyoxyethylene and polyoxypropylene (Pluronics); polymethacrylates; carbomers; and branched or unbranched polysaccharides which comprise the saccharide monomers such as D-mannose, D- and L- galactose, fucose, fructose, D-xylose, L-arabinose, and D-glucuronic acid.

[00184] In other embodiments, the biological modifier can be a hydrophilic polyvinyl polymer such as polyvinyl alcohol and polyvinylpyrrolidone (PVP)-type polymers. The biological modifier can be a functionalized polyvinylpyrrolidone, for example, carboxy or amine functionalized on one (or both) ends of the polymer (as available from PolymerSource).

Alternatively, the biological modifier can include Poly N-(2-hydroxypropyl)methacrylamide (HPMA), or functionalized HPMA (amine, carboxy, etc.), Poly(N-isopropylacrylamide) or functionalized poly(N-isopropylacrylamide). Alternatively, the biological modifier can include Poly N-(2-hydroxypropyl)methacrylamide (HPMA), or functionalized HPMA (amine, carboxy, etc.), Poly(N-isopropylacrylamide) or functionalized poly(N-isopropylacrylamide). The modifier prior to conjugation need not be, but preferably is, water soluble, but the final conjugate should be water soluble.

[00185] In general, the biological modifier may have a molecular weight from about 2 kDa to about 5 kDa, from about 2 kDa to about 10 kDa, from about 2 kDa to about 20 kDa, from about 2 kDa to about 30 kDa, from about 2 kDa to about 40 kDa, from about 2 kDa to about 50 kDa, from about 2 kDa to about 60 kDa, from about 2 kDa to about 70 kDa, from about 2 kDa to about 80 kDa, from about 2 kDa to about 90 kDa, from about 2 kDa to about 100 kDa, from about 2 kDa to about 150 kDa, from about 5 kDa to about 10 kDa, from about 5 kDa to about 20 kDa, from about 5 kDa to about 30 kDa, from about 5 kDa to about 40 kDa, from about 5 kDa to about 50 kDa, from about 5 kDa to about 60 kDa, from about 5 kDa to about 70 kDa, from about 5 kDa to about 80 kDa, from about 5 kDa to about 90 kDa, from about 5 kDa to about 100 kDa, from about 5 kDa to about 150 kDa, from about 10 kDa to about 20 kDa, from about 10 kDa to about 30 kDa, from about 10 kDa to about 40 kDa, from about 10 kDa to about 50 kDa, from about 10 kDa to about 60 kDa, from about 10 kDa to about 70 kDa, from about 10 kDa to about 80 kDa, from about 10 kDa to about 90 kDa, from about 10 kDa to about 100 kDa, from about 10 kDa to about 150 kDa, from about 20 kDa to about 30 kDa, from about 20 kDa to about 40 kDa, from about 20 kDa to about 50 kDa, from about 20 kDa to about 60 kDa, from about 20 kDa to about 70 kDa, from about 20 kDa to about 80 kDa, from about 20 kDa to about 90 kDa, from about 20 kDa to about 100 kDa, from about 20 kDa to about 150 kDa, from about 30 kDa to about 40 kDa, from about 30 kDa to about 50 kDa, from about 30 kDa to about 60 kDa, from about 30 kDa to about 70 kDa, from about 30 kDa to about 80 kDa, from about 30 kDa to about 90 kDa, from about 30 kDa to about 100 kDa, from about 30 kDa to about 150 kDa, from about 40 kDa to about 50 kDa, from about 40 kDa to about 60 kDa, from about 40 kDa to about 70 kDa, from about 40 kDa to about 80 kDa, from about 40 kDa to about 90 kDa, from about 40 kDa to about 100 kDa, from about 40 kDa to about 150 kDa, from about 50 kDa to about 60 kDa, from about 50 kDa to about 70 kDa, from about 50 kDa to about 80 kDa, from about 50 kDa to about 90 kDa, from about 50 kDa to about 100 kDa, from about 50 kDa to about 150 kDa, from about 60 kDa to about 70 kDa, from about 60 kDa to about 80 kDa, from about 60 kDa to about 90 kDa, from about 60 kDa to about 100 kDa, from about 60 kDa to about 150 kDa, from about 70 kDa to about 80 kDa, from about 70 kDa to about 90 kDa, from about 70 kDa to about 100 kDa, from about 70 kDa to about 150 kDa, from about 80 kDa to about 90 kDa, from about 80 kDa to about 100 kDa, from about 80 kDa to about 150 kDa, from about 90 kDa to about 100 kDa, from about 90 kDa to about 150 kDa, or from about 100 kDa to about 150 kDa.

[00186] It is contemplated that the antibody conjugate or fusion protein is attached to about 10 or fewer polymer molecules ( e.g 9, 8, 7, 6, 5, 4, 3, 2, or 1), each polymer molecule having a molecular weight of at least about 20,000 D, or at least about 30,000 D, or at least about 40,000 D.

[00187] Although a variety of polymers can be used as biological modifiers, it is contemplated that the antibody conjugates or fusion proteins described herein may be attached to polyethylene glycol (PEG) polymers. In one embodiment, the antibody conjugate or fusion protein described herein is covalently attached to at least one PEG having an actual MW of at least about 20,000 D. In another embodiment, the antibody conjugate or fusion protein described herein is covalently attached to at least one PEG having an actual MW of at least about 30,000 D. In another embodiment, the antibody conjugate or fusion protein described herein is covalently attached to at least one PEG having an actual MW of at least about 40,000 D. In certain embodiments, the PEG is methoxyPEG(5000)-succinimidylpropionate (mPEG-SPA), methoxyPEG(5000)-succinimidylsuccinate (mPEG-SS). Such PEGS are commercially available from Nektar Therapeutics or SunBiowest.

[00188] Attachment sites on an antibody conjugate or fusion protein for a biological modifier include the N-terminal amino group and epsilon amino groups found on lysine residues, as well as other amino, imino, carboxyl, sulfhydryl, hydroxyl or other hydrophilic groups. The polymer may be covalently bonded directly to the antibody conjugate or fusion protein with or without the known use of a multifunctional (ordinarily bifunctional) crosslinking agent using chemistries and used in the art. For example, sulfhydryl groups can be derivatized by coupling to maleimido-substituted PEG (e.g. alkoxy-PEG amine plus sulfosuccinimidyl 4-(N- maleimidomethyl)cyclohexane-l-carboxylate), or PEG-maleimide commercially available from Shearwater Polymers, Inc., Huntsville, Ala.).

II. Methods of Making a Fusion Protein or Antibody Conjugate

[00189] Methods for producing fusion proteins, e.g, those disclosed herein, antibodies, or antibody conjugates, e.g, those disclosed herein, are known in the art. For example, DNA molecules encoding light chain variable regions and/or heavy chain variable regions can be synthesized chemically or by recombinant DNA methodologies. For example, the sequences of the antibodies can be cloned from hybridomas by conventional hybridization techniques or polymerase chain reaction (PCR) techniques, using the appropriate synthetic nucleic acid primers. The resulting DNA molecules encoding the variable regions of interest can be ligated to other appropriate nucleotide sequences, including, for example, constant region coding sequences, and expression control sequences, to produce conventional gene expression constructs (i.e., expression vectors) encoding the desired antibodies. Production of defined gene constructs is within routine skill in the art.

[00190] Nucleic acids encoding desired fusion proteins, and/or antibody conjugates can be incorporated (ligated) into expression vectors, which can be introduced into host cells through conventional transfection or transformation techniques. Exemplary host cells are E. coli cells, Chinese hamster ovary (CHO) cells, human embryonic kidney 293 (HEK 293) cells, HeLa cells, baby hamster kidney (BHK) cells, monkey kidney cells (COS), human hepatocellular carcinoma cells (e.g, Hep G2), and myeloma cells that do not otherwise produce IgG protein. Transformed host cells can be grown under conditions that permit the host cells to express the genes that encode the immunoglobulin light and/or heavy chain variable regions.

[00191] Specific expression and purification conditions will vary depending upon the expression system employed. For example, if a gene is to be expressed in E. coli , it is first cloned into an expression vector by positioning the engineered gene downstream from a suitable bacterial promoter, e.g, Trp or Tac, and a prokaryotic signal sequence. The expressed protein may be secreted. The expressed protein may accumulate in refractile or inclusion bodies, which can be harvested after disruption of the cells by French press or sonication. The refractile bodies then are solubilized, and the protein may be refolded and/or cleaved by methods known in the art.

[00192] If the engineered gene is to be expressed in eukaryotic host cells, e.g, CHO cells, it is first inserted into an expression vector containing a suitable eukaryotic promoter, a secretion signal, a poly A sequence, and a stop codon. Optionally, the vector or gene construct may contain enhancers and introns. In embodiments involving fusion proteins comprising an antibody or portion thereof, the expression vector optionally contains sequences encoding all or part of a constant region, enabling an entire, or a part of, a heavy or light chain to be expressed. The gene construct can be introduced into eukaryotic host cells using conventional techniques.

[00193] The host cells express a fusion protein and/or antibody conjugate comprising a sialidase and VL or VH fragments, VL-VH heterodimers, VH-VL or VL-VH single chain polypeptides, complete heavy or light immunoglobulin chains, or portions thereof, each of which may be attached to a moiety having another function ( e.g ., cytotoxicity). In some embodiments involving fusion proteins and/or antibody conjugates, a host cell is transfected with a single vector expressing a polypeptide expressing a sialidase and an entire, or part of, a heavy chain (e.g., a heavy chain variable region) or a sialidase and a light chain (e.g, a light chain variable region), or a polypeptide expressing an entire, or part of, a heavy chain (e.g, a heavy chain variable region) or a light chain (e.g, a light chain variable region). In some embodiments, a host cell is transfected with a single vector encoding (a) a polypeptide comprising a heavy chain variable region and a polypeptide comprising a light chain variable region, or (b) an entire immunoglobulin heavy chain and an entire immunoglobulin light chain, wherein in (a) or in (b), the polypeptide may also comprise a sialidase. In some embodiments, a host cell is co transfected with more than one expression vector (e.g, one expression vector expressing a polypeptide comprising an entire, or part of, a heavy chain or heavy chain variable region, optionally comprising a sialidase fused thereto, and another expression vector expressing a polypeptide comprising an entire, or part of, a light chain or light chain variable region, optionally comprising a sialidase fused thereto).

[00194] A polypeptide comprising a fusion protein, e.g, a fusion protein comprising an immunoglobulin heavy chain variable region or light chain variable region, can be produced by growing (culturing) a host cell transfected with an expression vector encoding such a variable region, under conditions that permit expression of the polypeptide. Following expression, the polypeptide can be harvested and purified or isolated using techniques known in the art, e.g, affinity tags such as glutathione-S-transferase (GST) or histidine tags.

[00195] In embodiments in which a fusion protein and/or antibody conjugate is produced, a sialidase fused to a monoclonal antibody, Fc domain, or an antigen-binding domain of the antibody, can be produced by growing (culturing) a host cell transfected with: (a) an expression vector that encodes a complete or partial immunoglobulin heavy chain, and a separate expression vector that encodes a complete or partial immunoglobulin light chain; or (b) a single expression vector that encodes both chains ( e.g ., complete or partial heavy and light chains), under conditions that permit expression of both chains. The sialidase will be fused to one or more of the chains. The intact fusion protein and/or antibody conjugate can be harvested and purified or isolated using techniques known in the art, e.g., Protein A, Protein G, affinity tags such as glutathione-S-transferase (GST) or histidine tags. It is within ordinary skill in the art to express the heavy chain and the light chain from a single expression vector or from two separate expression vectors.

[00196] In certain embodiments, in order to express a protein, e.g, a fusion protein, as a secreted protein, a native N-terminal signal sequence of the protein is replaced, e.g, with MDMRVPAQLLGLLLLWLPGARC (SEQ ID NO: 28). In certain embodiments, to express a protein, e.g, a fusion protein, as a secreted protein, an N-terminal signal sequence, e.g,

MDMRVPAQLLGLLLLWLPGARC (SEQ ID NO: 28), is added. Additional exemplary N- terminal signal sequences include signal sequences from interleukin-2, CD-5, IgG kappa light chain, trypsinogen, serum albumin, and prolactin. In certain embodiments, in order to express a protein, e.g, a fusion protein, as a secreted protein, a C terminal lysosomal signal motif, e.g, YGTL (SEQ ID NO: 29) is removed.

[00197] Methods for reducing or eliminating the antigenicity of antibodies and antibody fragments are known in the art. When the antibodies are to be administered to a human, the antibodies preferably are“humanized” to reduce or eliminate antigenicity in humans.

Preferably, each humanized antibody has the same or substantially the same affinity for the antigen as the non-humanized mouse antibody from which it was derived.

[00198] In one humanization approach, chimeric proteins are created in which mouse immunoglobulin constant regions are replaced with human immunoglobulin constant regions. See, e.g., Morrison et al, 1984, PROC. NAT. ACAD. SCI. 81 :6851-6855, Neuberger et al, 1984, NATURE 312:604-608; U.S. Patent Nos. 6,893,625 (Robinson); 5,500,362 (Robinson); and 4,816,567 (Cabilly).

[00199] In an approach known as CDR grafting, the CDRs of the light and heavy chain variable regions are grafted into frameworks from another species. For example, murine CDRs can be grafted into human FRs. In some embodiments, the CDRs of the light and heavy chain variable regions of an antibody are grafted into human FRs or consensus human FRs. To create consensus human FRs, FRs from several human heavy chain or light chain amino acid sequences are aligned to identify a consensus amino acid sequence. CDR grafting is described in U.S. Patent Nos. 7,022,500 (Queen); 6,982,321 (Winter); 6,180,370 (Queen); 6,054,297 (Carter); 5,693,762 (Queen); 5,859,205 (Adair); 5,693,761 (Queen); 5,565,332 (Hoogenboom); 5,585,089 (Queen); 5,530,101 (Queen); Jones et al. (1986) NATURE 321 : 522-525; Riechmann et al. (1988) NATURE 332: 323-327; Verhoeyen et al. (1988) SCIENCE 239: 1534-1536; and Winter (1998) FEBS LETT 430: 92-94.

[00200] In an approach called“SUPERHUMANIZATION'' ¹ ,” human CDR sequences are chosen from human germline genes, based on the structural similarity of the human CDRs to those of the mouse antibody to be humanized. See, e.g ., U.S. Patent No. 6,881,557 (Foote); and Tan et al. , 2002, J. IMMUNOL. 169: 1 1 19-1 125.

[00201] Other methods to reduce immunogenicity include“reshaping,”“hyperchimerization,” and“veneering/resurfacing.” See, e.g. , Vaswami et al, 1998, ANNALS OF ALLERGY, ASTHMA, & IMMUNOL. 81 : 105; Roguska et al., 1996, PROT. ENGINEER 9: 895-904; and U.S. Patent No.

6,072,035 (Hardman). In the veneering/resurfacing approach, the surface accessible amino acid residues in the murine antibody are replaced by amino acid residues more frequently found at the same positions in a human antibody. This type of antibody resurfacing is described, e.g, in U.S. Patent No. 5,639,641 (Pedersen).

[00202] Another approach for converting a mouse antibody into a form suitable for medical use in humans is known as ACTIVMAB ^™ technology (Vaccinex, Inc., Rochester, NY), which involves a vaccinia virus-based vector to express antibodies in mammalian cells. High levels of combinatorial diversity of IgG heavy and light chains can be produced. See, e.g, U.S. Patent Nos. 6,706,· 477 (Zauderer); 6,800,442 (Zauderer); and 6,872,518 (Zauderer). Another approach for converting a mouse antibody into a form suitable for use in humans is technology practiced commercially by KaloBios Pharmaceuticals, Inc. (Palo Alto, CA). This technology involves the use of a proprietary human“acceptor” library to produce an“epitope focused” library for antibody selection. Another approach for modifying a mouse antibody into a form suitable for medical use in humans is HUMAN ENGINEERING ^™ technology, which is practiced commercially by XOMA (US) LLC. See, e.g, International (PCT) Publication No. WO

93/11794 and U.S. Patent Nos. 5,766,886 (Studnicka); 5,770,196 (Studnicka); 5,821,123 (Studnicka); and 5,869,619 (Studnicka).

[00203] Any suitable approach, including any of the above approaches, can be used to reduce or eliminate human immunogenicity of an antibody.

[00204] In addition, it is possible to create fully human antibodies in mice. Fully human mAbs lacking any non-human sequences can be prepared from human immunoglobulin transgenic mice by techniques referenced in, e.g., Lonberg et al., NATURE 368:856-859, 1994; Fishwild et al., NATURE BIOTECHNOLOGY 14:845-851, 1996; and Mendez et al, NATURE GENETICS 15: 146-156, 1997. Fully human monoclonal antibodies can also be prepared and optimized from phage display libraries by techniques referenced in, e.g. , Knappik et al., J. MOL. BIOL. 296:57- 86, 2000; and Krebs et al. , J. IMMUNOL. METH. 254:67-84 2001).

[00205] The present invention encompasses fusion proteins comprising antibody fragments, which may be generated by traditional means, such as enzymatic digestion, or by recombinant techniques. For a review of certain antibody fragments, see Hudson et al. (2003) NAT. MED. 9: 129-134.

[00206] Various techniques have been developed for the production of antibody fragments. Traditionally, these fragments were derived via proteolytic digestion of intact antibodies (see, e.g, Morimoto et al. (1992) JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS 24:107- 117; and Brennan et al. (1985) SCIENCE 229:81). However, these fragments can now be produced directly by recombinant host cells. Fab, Fv and ScFv antibody fragments can all be expressed in and secreted from E. coli, thus allowing the facile production of large amounts of these fragments. Antibody fragments can be isolated from the antibody phage libraries.

Alternatively, Fab’-SH fragments can be directly recovered from E. coli and chemically coupled to form F(ab’) ₂ fragments (Carter et al. (1992) BIO/TECHNOLOGY 10: 163-167). According to another approach, F(ab’) ₂ fragments can be isolated directly from recombinant host cell culture. Fab and F(ab’) ₂ fragments with increased in vivo half-life comprising salvage receptor binding epitope residues are described in U.S. Patent No. 5,869,046. Other techniques for the production of antibody fragments will be apparent to the skilled practitioner. In certain embodiments, an antibody is a single chain Fv fragment (scFv). See U.S. Patent Nos. 5,571,894 and 5,587,458.

[00207] Methods for making bispecific antibodies are known in the art. See Milstein and Cuello (1983) NATURE 305:537, International (PCT) Publication No. WO93/08829, and Traunecker et al. (1991) EMBO J., 10:3655. For further details of generating bispecific antibodies see, for example, Suresh el al. (1986) METHODS ENZYMOL. 121 :210. Bispecific antibodies include cross-linked or“heteroconjugate” or“heterodimer” antibodies. For example, one of the antibodies in the heterodimer can be coupled to avidin, the other to biotin. Heterodimer antibodies may be made using any convenient cross-linking method. Suitable cross-linking agents are well known in the art, and are disclosed in U.S. Patent No. 4,676,980, along with a number of cross-linking techniques. [00208] Examples of heterodimeric or asymmetric IgG-like molecules include but are not limited to those obtained with the following technologies or using the following formats:

Triomab/Quadroma, Knobs-into-Holes, CrossMabs, electrostatically-matched antibodies, LUZ- Y, Strand Exchange Engineered Domain body, Biclonic and DuoBody.

[00209] Advantages of using antibody fragments ( e.g ., F(ab) and F(ab’)2 fragments) include the elimination of non-specific binding between Fc portions of antibodies and Fc receptors on cells (such as macrophages, dendritic cells, neutrophils, NK cells and B cells). In addition, they may be able to penetrate tissues more efficiently due to their smaller size.

[00210] Heterodimeric antibodies, or asymmetric antibodies, allow for greater flexibility and new formats for attaching a variety of drugs to the antibody arms. One of the general formats for creating a heterodimeric antibody is the“knobs-into-holes” format. This format is specific to the heavy chain part of the constant region in antibodies. The“knobs” part is engineered by replacing a small amino acid with a larger one, which fits into a“hole”, which is engineered by replacing a large amino acid with a smaller one. What connects the“knobs” to the“holes” are the disulfide bonds between each chain. The“knobs-into-holes” shape facilitates antibody dependent cell mediated cytotoxicity. Single chain variable fragments (scFv) are connected to the variable domain of the heavy and light chain via a short linker peptide. The linker is rich in glycine, which gives it more flexibility, and serine/threonine, which gives it specificity. Two different scFv fragments can be connected together, via a hinge region, to the constant domain of the heavy chain or the constant domain of the light chain. This gives the antibody bispecificity, allowing for the binding specificities of two different antigens. The“knobs-into-holes” format enhances heterodimer formation but doesn’t suppress homodimer formation.

[00211] Several approaches to support heterodimerization have been described, for example in International (PCT) Publication Nos. WO96/27011, W098/050431, W02007/110205,

W02007/147901, W02009/089004, W02010/129304, WO2011/90754, WO2011/143545, WO2012/058768, WO2013/157954, and WO2013/096291, and European Patent Publication No. EP 1870459. Typically, in the approaches known in the art, the C¾ domain of the first heavy chain and the C¾ domain of the second heavy chain are both engineered in a complementary manner so that the heavy chain comprising one engineered C¾ domain can no longer homodimerize with another heavy chain of the same structure (e.g. a CH3-engineered first heavy chain can no longer homodimerize with another CH3-engineered first heavy chain; and a CH3- engineered second heavy chain can no longer homodimerize with another CH3-engineered second heavy chain). Thereby the heavy chain comprising one engineered CH3 domain is forced to heterodimerize with another heavy chain comprising the CH ₃ domain, which is engineered in a complementary manner. As a result, the CH ₃ domain of the first heavy chain and the CH ₃ domain of the second heavy chain are engineered in a complementary manner by amino acid substitutions, such that the first heavy chain and the second heavy chain are forced to

heterodimerize, whereas the first heavy chain and the second heavy chain can no longer homodimerize (e.g, for steric reasons).

III. Pharmaceutical Compositions

[00212] For therapeutic use, a fusion protein and/or antibody conjugate preferably is combined with a pharmaceutically acceptable carrier. The term“pharmaceutically acceptable” as used herein refers to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.

[00213] The term“pharmaceutically acceptable carrier” as used herein refers to buffers, carriers, and excipients suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio. Pharmaceutically acceptable carriers include any of the standard pharmaceutical carriers, such as a phosphate buffered saline solution, water, emulsions (e.g, such as an oil/water or water/oil emulsions), and various types of wetting agents. The compositions also can include stabilizers and preservatives. For examples of carriers, stabilizers and adjuvants, see, e.g, Martin, Remington’s Pharmaceutical Sciences, 15th Ed., Mack Publ. Co., Easton, PA [1975] Pharmaceutically acceptable carriers include buffers, solvents, dispersion media, coatings, isotonic and absorption delaying agents, and the like, that are compatible with pharmaceutical administration. The use of such media and agents for pharmaceutically active substances is known in the art.

[00214] In certain embodiments, a pharmaceutical composition may contain formulation materials for modifying, maintaining or preserving, for example, the pH, osmolarity, viscosity, clarity, color, isotonicity, odor, sterility, stability, rate of dissolution or release, adsorption or penetration of the composition. In such embodiments, suitable formulation materials include, but are not limited to, amino acids (such as glycine, glutamine, asparagine, arginine or lysine); antimicrobials; antioxidants (such as ascorbic acid, sodium sulfite or sodium hydrogen-sulfite); buffers (such as borate, bicarbonate, Tris-HCl, citrates, phosphates or other organic acids);

bulking agents (such as mannitol or glycine); chelating agents (such as ethylenediamine tetraacetic acid (EDTA)); complexing agents (such as caffeine, polyvinylpyrrolidone, beta- cyclodextrin or hydroxypropyl-beta-cyclodextrin); fillers; monosaccharides; disaccharides; and other carbohydrates (such as glucose, mannose or dextrins); proteins (such as serum albumin, gelatin or immunoglobulins); coloring, flavoring and diluting agents; emulsifying agents;

hydrophilic polymers (such as polyvinylpyrrolidone); low molecular weight polypeptides; salt forming counterions (such as sodium); preservatives (such as benzalkonium chloride, benzoic acid, salicylic acid, thimerosal, phenethyl alcohol, methylparaben, propylparaben, chlorhexidine, sorbic acid or hydrogen peroxide); solvents (such as glycerin, propylene glycol or polyethylene glycol); sugar alcohols (such as mannitol or sorbitol); suspending agents; surfactants or wetting agents (such as pluronics, PEG, sorbitan esters, polysorbates such as polysorbate 20,

polysorbate, triton, tromethamine, lecithin, cholesterol, tyloxapal); stability enhancing agents (such as sucrose or sorbitol); tonicity enhancing agents (such as alkali metal halides, preferably sodium or potassium chloride, mannitol sorbitol); delivery vehicles; diluents; excipients and/or pharmaceutical adjuvants (see, Remington’s Pharmaceutical Sciences , 18th ed. (Mack

Publishing Company, 1990).

[00215] In certain embodiments, a pharmaceutical composition may contain nanoparticles, e.g, polymeric nanoparticles, liposomes, or micelles (See Anselmo et al. (2016) BIOENG. TRANSL. MED. 1 : 10-29).

[00216] In certain embodiments, a pharmaceutical composition may contain a sustained- or controlled-delivery formulation. Techniques for formulating sustained- or controlled-delivery means, such as liposome carriers, bio-erodible microparticles or porous beads and depot injections, are also known to those skilled in the art. Sustained-release preparations may include, e.g. , porous polymeric microparticles or semipermeable polymer matrices in the form of shaped articles, e.g, films, or microcapsules. Sustained release matrices may include polyesters, hydrogels, polylactides, copolymers of L-glutamic acid and gamma ethyl -L-glutamate, poly (2- hydroxyethyl-inethacrylate), ethylene vinyl acetate, or poly-D(-)-3-hydroxybutyric acid.

Sustained release compositions may also include liposomes that can be prepared by any of several methods known in the art.

[00217] Pharmaceutical compositions containing a sialidase fusion protein or an antibody conjugate disclosed herein can be presented in a dosage unit form and can be prepared by any suitable method. A pharmaceutical composition should be formulated to be compatible with its intended route of administration. Examples of routes of administration are intravenous (IV), intradermal, inhalation, transdermal, topical, transmucosal, intrathecal and rectal administration. In certain embodiments, a sialidase fusion protein or an antibody conjugate disclosed herein is administered by IV infusion. In certain embodiments, a sialidase fusion protein or an antibody conjugate disclosed herein is administered by intratumoral injection. Useful formulations can be prepared by methods known in the pharmaceutical art. For example, see Remington’s

Pharmaceutical Sciences, 18th ed. (Mack Publishing Company, 1990). Formulation

components suitable for parenteral administration include a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerin, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as EDTA; buffers such as acetates, citrates or phosphates; and agents for the adjustment of tonicity such as sodium chloride or dextrose.

[00218] For intravenous administration, suitable carriers include physiological saline, bacteriostatic water, Cremophor ELTM (BASF, Parsippany, NJ) or phosphate buffered saline (PBS). The carrier should be stable under the conditions of manufacture and storage, and should be preserved against microorganisms. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol), and suitable mixtures thereof.

[00219] In certain embodiments, a pharmaceutical composition may contain a stabilizing agent. In certain embodiments, the stabilizing agent is a cation, such as a divalent cation. In certain embodiments, the cation is calcium or magnesium. The cation can be in the form of a salt, such as calcium chloride (CaCh) or magnesium chloride (MgCh).

[00220] In certain embodiments, the stabilizing agent is present in an amount from about 0.05 mM to about 5 mM. For example, the stabilizing agent may be present in an amount of from about 0.05 mM to about 4 mM, from about 0.05 mM to about 3 mM, from about 0.05 mM to about 2 mM, from about 0.05 mM to about 1 mM, from about 0.05 mM to about 0.5 mM, from about 0.5 mM to about 4 mM, from about 0.5 mM to about 3 mM, from about 0.5 mM to about 2 mM, from about 0.5 mM to about 1 mM, from about 1 mM to about 4 mM, from about 1 mM to about 3 mM, of from about 1 mM to about 2 mM.

[00221] Pharmaceutical formulations preferably are sterile. Sterilization can be accomplished by any suitable method, e.g. , filtration through sterile filtration membranes. Where the composition is lyophilized, filter sterilization can be conducted prior to or following

lyophilization and reconstitution. [00222] The compositions described herein may be administered locally or systemically.

Administration will generally be parenteral administration. In a preferred embodiment, the pharmaceutical composition is administered subcutaneously and in an even more preferred embodiment intravenously. Preparations for parenteral administration include sterile aqueous or non-aqueous solutions, suspensions, and emulsions.

[00223] Generally, a therapeutically effective amount of active component, for example, a fusion protein and/or antibody conjugate, is in the range of 0.1 mg/kg to 100 mg/kg, e.g ., 1 mg/kg to 100 mg/kg, 1 mg/kg to 10 mg/kg. The amount administered will depend on variables such as the type and extent of disease or indication to be treated, the overall health of the patient, the in vivo potency of the antibody, the pharmaceutical formulation, and the route of

administration. The initial dosage can be increased beyond the upper level in order to rapidly achieve the desired blood-level or tissue-level. Alternatively, the initial dosage can be smaller than the optimum, and the daily dosage may be progressively increased during the course of treatment. Human dosage can be optimized, e.g. , in a conventional Phase I dose escalation study designed to run from 0.5 mg/kg to 20 mg/kg. Dosing frequency can vary, depending on factors such as route of administration, dosage amount, serum half-life of the fusion protein and/or antibody conjugate, and the disease being treated. Exemplary dosing frequencies are once per day, once per week and once every two weeks. A preferred route of administration is parenteral, e.g. , intravenous infusion. In certain embodiments, a fusion protein and/or antibody conjugate is lyophilized, and then reconstituted in buffered saline, at the time of administration.

IV. Therapeutic Uses

[00224] The compositions and methods disclosed herein can be used to treat various forms of cancer in a subject or inhibit cancer growth in a subject. The invention provides a method of treating a cancer in a subject. The method comprises administering to the subject an effective amount of a sialidase anti-PD-Ll fusion protein and/or antibody conjugate, e.g, a fusion protein or antibody conjugate disclosed herein, either alone or in a combination with another therapeutic agent to treat the cancer in the subject. The term“effective amount” as used herein refers to the amount of an active agent (e.g, fusion protein according to the present invention) sufficient to effect beneficial or desired results. An effective amount can be administered in one or more administrations, applications or dosages and is not intended to be limited to a particular formulation or administration route.

[00225] As used herein,“treat”,“treating” and“treatment” mean the treatment of a disease in a subject, e.g, in a human. This includes: (a) inhibiting the disease, i.e., arresting its development; and (b) relieving the disease, i.e., causing regression of the disease state. As used herein, the terms“subject” and“patient” refer to an organism to be treated by the methods and compositions described herein. Such organisms preferably include, but are not limited to, mammals ( e.g ., murines, simians, equines, bovines, porcines, canines, felines, and the like), and more preferably includes humans.

[00226] Examples of cancers include solid tumors, soft tissue tumors, hematopoietic tumors and metastatic lesions. Examples of hematopoietic tumors include, leukemia, acute leukemia, acute lymphoblastic leukemia (ALL), B-cell, T-cell or FAB ALL, acute myeloid leukemia (AML), chronic myelocytic leukemia (CML), chronic lymphocytic leukemia (CLL), e.g., transformed CLL, diffuse large B-cell lymphomas (DLBCL), follicular lymphoma, hairy cell leukemia, myelodyplastic syndrome (MDS), a lymphoma, Hodgkin’s disease, a malignant lymphoma, non- Hodgkin’s lymphoma, Burkitt’s lymphoma, multiple myeloma, or Richter’s Syndrome

(Richter’s Transformation). Examples of solid tumors include malignancies, e.g, sarcomas, adenocarcinomas, and carcinomas, of the various organ systems, such as those affecting head and neck (including pharynx), thyroid, lung (small cell or non-small cell lung carcinoma

(NSCLC)), breast, lymphoid, gastrointestinal (e.g, oral, esophageal, stomach, liver, pancreas, small intestine, colon and rectum, anal canal), genitals and genitourinary tract (e.g, renal, urothelial, bladder, ovarian, uterine, cervical, endometrial, prostate, testicular), CNS (e.g, neural or glial cells, e.g, neuroblastoma or glioma), or skin (e.g, melanoma and metastatic Merkel cell carcinoma (MCC)).

[00227] In certain embodiments the cancer is an epithelial cancer, e.g, an epithelial cancer that upregulates the expression of sialylated glycans. Exemplary epithelial cancers include, but are not limited to, endometrial cancer, colon cancer, ovarian cancer, cervical cancer, vulvar cancer, uterine cancer or fallopian tube cancer, breast cancer, prostate cancer, lung cancer, pancreatic cancer, urinary cancer, bladder cancer, head and neck cancer, oral cancer and liver cancer.

Epithelial cancers also include carcinomas, for example, acinar carcinoma, acinous carcinoma, adenocystic carcinoma, adenoid cystic carcinoma, carcinoma adenomatosum, carcinoma of adrenal cortex, alveolar carcinoma, alveolar cell carcinoma, basal cell carcinoma, carcinoma basocellulare, basaloid carcinoma, baso squamous cell carcinoma, bronchioalveolar carcinoma, bronchiolar carcinoma, bronchogenic carcinoma, cerebriform carcinoma, cholangiocellular carcinoma, chorionic carcinoma, colloid carcinoma, comedo carcinoma, corpus carcinoma, cribriform carcinoma, carcinoma en cuirasse, carcinoma cutaneum, cylindrical carcinoma, cylindrical cell carcinoma, duct carcinoma, carcinoma durum, embryonal carcinoma,

encephaloid carcinoma, epiermoid carcinoma, carcinoma epitheliale adenoides, exophytic carcinoma, carcinoma ex ulcere, carcinoma fibrosum, gelatiniforni carcinoma, gelatinous carcinoma, giant cell carcinoma, carcinoma gigantocellulare, glandular carcinoma, granulosa cell carcinoma, hair-matrix carcinoma, hematoid carcinoma, hepatocellular carcinoma, Hurthle cell carcinoma, hyaline carcinoma, hypemephroid carcinoma, infantile embryonal carcinoma, carcinoma in situ, intraepidermal carcinoma, intraepithelial carcinoma, Krompecher’s carcinoma, Kulchitzky-cell carcinoma, large-cell carcinoma, lenticular carcinoma, carcinoma lenticulare, lipomatous carcinoma, lymphoepithelial carcinoma, carcinoma medullare, medullary carcinoma, melanotic carcinoma, carcinoma molle, mucinous carcinoma, carcinoma muciparum, carcinoma mucocellulare, mucoepidermoid carcinoma, carcinoma mucosum, mucous carcinoma, carcinoma myxomatodes, nasopharyngeal carcinoma, oat cell carcinoma, carcinoma ossificans, osteoid carcinoma, papillary carcinoma, periportal carcinoma, preinvasive carcinoma, prickle cell carcinoma, pultaceous carcinoma, renal cell carcinoma of kidney, reserve cell carcinoma, carcinoma sarcomatodes, Schneiderian carcinoma, scirrhous carcinoma, carcinoma scroti, signet ring cell carcinoma, carcinoma simplex, small-cell carcinoma, solanoid carcinoma, spheroidal cell carcinoma, spindle cell carcinoma, carcinoma spongiosum, squamous carcinoma, squamous cell carcinoma, string carcinoma, carcinoma telangiectaticum, carcinoma telangiectodes, transitional cell carcinoma, carcinoma tuberosum, tuberous carcinoma, verrucous carcinoma, and carcinoma villosum.

[00228] In certain embodiments the cancer is selected from lung bronchioloalveolar carcinoma (BAC), bladder cancer, a female genital tract malignancy ( e.g ., uterine serous carcinoma, endometrial carcinoma, vulvar squamous cell carcinoma, and uterine sarcoma), an ovarian surface epithelial carcinoma (e.g., clear cell carcinoma of the ovary, epithelial ovarian cancer, fallopian tube cancer, and primary peritoneal cancer), breast carcinoma, non-small cell lung cancer (NSCLC), a male genital tract malignancy (e.g, testicular cancer), retroperitoneal or peritoneal carcinoma, gastroesophageal adenocarcinoma, esophagogastric junction carcinoma, liver hepatocellular carcinoma, esophageal and esophagogastric junction carcinoma, cervical cancer, cholangiocarcinoma, pancreatic adenocarcinoma, extrahepatic bile duct adenocarcinoma, a small intestinal malignancy, gastric adenocarcinoma, cancer of unknown primary (CUP), colorectal adenocarcinoma, esophageal carcinoma, prostatic adenocarcinoma, kidney cancer, head and neck squamous carcinoma, thymic carcinoma, non-melanoma skin cancer, thyroid carcinoma (e.g, papillary carcinoma), a head and neck cancer, anal carcinoma, non-epithelial ovarian cancer (non-EOC), metastatic urothelial carcinoma (UC), uveal melanoma, malignant pleural mesothelioma, small cell lung cancer (SCLC), a central nervous system cancer, a neuroendocrine tumor, and a soft tissue tumor. [00229] In certain embodiments, the cancer is melanoma, non-small cell lung cancer, colon cancer, breast cancer, bladder cancer, or kidney cancer.

[00230] In certain embodiments, the cancer is an adenocarcinoma. In certain embodiments, the cancer is a metastatic cancer. In certain embodiments, the cancer is a refractory cancer.

[00231] In certain embodiments, the cancer is resistant to or non-responsive to treatment with an antibody, e.g., an antibody with ADCC activity, e.g, avelumab.

[00232] In certain embodiments, the cancer is a PD-L1 -expressing cancer, e.g. , the cancer comprises cells that express PD-L1. An analysis of 196 tumor specimens from patients with renal cell carcinoma found that high tumor expression of PD-L1 was associated with increased tumor aggressiveness and a 4.5-fold increased risk of death. High expression of PD-L1 is associated with reduced numbers of tumor infiltrating lymphocytes and poor prognosis. In certain embodiments, the PD-L1 status of a cancer can be determined using

immunohistochemistry staining protocols, such as DAKO 22C3 and VENT ANA SP142 FDA approved protocols, which are used as companion diagnostics for anti-PD-Ll antibodies pembrolizumab, durvalumab, atezolizumab, and avelumab.

[00233] The methods and compositions described herein can be used alone or in combination with other therapeutic agents and/or modalities. The term administered“in combination,” as used herein, is understood to mean that two (or more) different treatments are delivered to the subject during the course of the subject’s affliction with the disorder, such that the effects of the treatments on the patient overlap at a point in time. In certain embodiments, the delivery of one treatment is still occurring when the delivery of the second begins, so that there is overlap in terms of administration. This is sometimes referred to herein as“simultaneous” or“concurrent delivery.” In other embodiments, the delivery of one treatment ends before the delivery of the other treatment begins. In certain embodiments of either case, the treatment is more effective because of combined administration. For example, the second treatment is more effective, e.g. , an equivalent effect is seen with less of the second treatment, or the second treatment reduces symptoms to a greater extent, than would be seen if the second treatment were administered in the absence of the first treatment, or the analogous situation is seen with the first treatment. In certain embodiments, delivery is such that the reduction in a symptom, or other parameter related to the disorder is greater than what would be observed with one treatment delivered in the absence of the other. The effect of the two treatments can be partially additive, wholly additive, or greater than additive. The delivery can be such that an effect of the first treatment delivered is still detectable when the second is delivered. [00234] In certain embodiments, a method or composition described herein, is administered in combination with one or more additional therapies, e.g ., surgery, radiation therapy, or administration of another therapeutic preparation. In certain embodiments, the additional therapy may include chemotherapy, e.g. , a cytotoxic agent. In certain embodiments the additional therapy may include a targeted therapy, e.g. a tyrosine kinase inhibitor, a proteasome inhibitor, or a protease inhibitor. In certain embodiments, the additional therapy may include an anti-inflammatory, anti-angiogenic, anti-fibrotic, or anti -proliferative compound, e.g. , a steroid, a biologic immunomodulator, a monoclonal antibody, an antibody fragment, an aptamer, an siRNA, an antisense molecule, a fusion protein, a cytokine, a cytokine receptor, a

bronchodialator, a statin, an anti-inflammatory agent (e.g. methotrexate), or an NSAID. In certain embodiments, the additional therapy may include a combination of therapeutics of different classes.

[00235] In certain embodiments, a method or composition described herein is administered in combination with a second checkpoint inhibitor. The checkpoint inhibitor may, for example, be selected from a PD-1 antagonist, a second PD-L1 antagonist, CTLA-4 antagonist, adenosine A2A receptor antagonist, B7-H3 antagonist, B7-H4 antagonist, BTLA antagonist, KIR antagonist, LAG3 antagonist, TIM-3 antagonist, VISTA antagonist or TIGIT antagonist.

[00236] In certain embodiments, the checkpoint inhibitor is a PD-1 or a second PD-L1 inhibitor. PD-1 is a receptor present on the surface of T-cells that serves as an immune system checkpoint that inhibits or otherwise modulates T-cell activity at the appropriate time to prevent an overactive immune response. Cancer cells, however, can take advantage of this checkpoint by expressing ligands, for example, PD-L1, that interact with PD-1 on the surface of T-cells to shut down or modulate T-cell activity. Exemplary PD-1/PD-L1 based immune checkpoint inhibitors include antibody based therapeutics. Exemplary treatment methods that employ PD- 1/PD-Ll based immune checkpoint inhibition are described in U.S. Patent Nos. 8,728,474 and 9,073,994, and EP Patent No. 1537878B1, and, for example, include the use of anti-PD-1 antibodies. Exemplary anti-PD-1 antibodies are described, for example, in U.S. Patent Nos.

8,952,136, 8,779,105, 8,008,449, 8,741,295, 9,205,148, 9,181,342, 9,102,728, 9,102,727,

8,952,136, 8,927,697, 8,900,587, 8,735,553, and 7,488,802. Exemplary anti-PD-1 antibodies include, for example, nivolumab (Opdivo®, Bristol-Myers Squibb Co.), pembrolizumab

(Keytruda®, Merck Sharp & Dohme Corp.), PDR001 (Novartis Pharmaceuticals), and pidilizumab (CT-011, Cure Tech). Exemplary anti-PD-Ll antibodies are described, for example, in U.S. Patent Nos. 9,273,135, 7,943,743, 9,175,082, 8,741,295, 8,552,154, and 8,217,149. Exemplary anti-PD-Ll antibodies include, atezolizumab (Tecentriq®, Genentech), durvalumab (AstraZeneca), MEDI4736, avelumab, and BMS 936559 (Bristol Myers Squibb Co.).

[00237] In certain embodiments, a method or composition described herein is administered in combination with a CTLA-4 inhibitor. In the CTLA-4 pathway, the interaction of CTLA-4 on a T-cell with its ligands ( e.g ., CD80, also known as B7-1, and CD86) on the surface of an antigen presenting cells (rather than cancer cells) leads to T-cell inhibition. Exemplary CTLA-4 based immune checkpoint inhibition methods are described in U.S. Patent Nos. 5,811,097, 5,855,887, 6,051,227. Exemplary anti-CTLA-4 antibodies are described in U.S. Patent Nos. 6,984,720,

6,682,736, 7,311,910: 7,307,064, 7,109,003, 7,132,281, 6,207,156, 7,807,797, 7,824,679

8,143,379, 8,263,073, 8,318,916, 8,017,114, 8,784,815, and 8,883,984, International (PCT) Publication Nos. W098/42752, WO00/37504, and WOOl/14424, and European Patent No. EP 1212422 Bl. Exemplary CTLA-4 antibodies include ipilimumab or tremelimumab.

[00238] In certain embodiments, a method or composition described herein is administered in combination with a CTLA-4 inhibitor, e.g., a CTLA-4 inhibitor disclosed herein.

[00239] In certain embodiments, a method or composition described herein is administered in combination with an IDO inhibitor. Exemplary IDO inhibitors include 1 -methyl -D-tryptophan (known as indoximod), epacadostat (INCB24360), navoximod (GDC-0919), and BMS-986205.

[00240] Exemplary cytotoxic agents that can be administered in combination with a method or composition described herein include, for example, antimicrotubule agents, topoisomerase inhibitors, antimetabolites, protein synthesis and degradation inhibitors, mitotic inhibitors, alkylating agents, platinating agents, inhibitors of nucleic acid synthesis, histone deacetylase inhibitors (HDAC inhibitors, e.g., vorinostat (SAHA, MK0683), entinostat (MS-275), panobinostat (LBH589), trichostatin A (TSA), mocetinostat (MGCD0103), belinostat

(PXD101), romidepsin (FK228, depsipeptide)), DNA methyltransferase inhibitors, nitrogen mustards, nitrosoureas, ethylenimines, alkyl sulfonates, triazenes, folate analogs, nucleoside analogs, ribonucleotide reductase inhibitors, vinca alkaloids, taxanes, epothilones, intercalating agents, agents capable of interfering with a signal transduction pathway, agents that promote apoptosis and radiation, or antibody molecule conjugates that bind surface proteins to deliver a toxic agent. In one embodiment, the cytotoxic agent that can be administered with a method or composition described herein is a platinum-based agent (such as cisplatin), cyclophosphamide, dacarbazine, methotrexate, fluorouracil, gemcitabine, capecitabine, hydroxyurea, topotecan, irinotecan, azacytidine, vorinostat, ixabepilone, bortezomib, taxanes (e.g, paclitaxel or docetaxel), cytochalasin B, gramicidin D, ethidium bromide, emetine, mitomycin, etoposide, tenoposide, vincristine, vinblastine, vinorelbine, colchicin, anthracyclines ( e.g ., doxorubicin or epirubicin) daunorubicin, dihydroxy anthracin dione, mitoxantrone, mithramycin, actinomycin D, adriamycin, 1 -dehydrotestosterone, glucocorticoids, procaine, tetracaine, lidocaine, propranolol, puromycin, ricin, or maytansinoids.

[00241] The invention also provides a method of increasing the expression of HLA-DR, CD86, CD83, IENg, IL-lb, IL-6, TNFa, IL-17A, IL-2, or IL-6 in a cell, tissue, or subject. The method comprises contacting the cell, tissue, or subject with an effective amount of a fusion protein and/or antibody conjugate, e.g., a fusion protein or antibody conjugate disclosed herein. In certain embodiments, the cell is selected from a dendritic cell and a peripheral blood

mononuclear cell (PBMC).

[00242] In certain embodiments, expression of HLA-DR, CD86, CD83, IFNy, IL-lb, IL-6, TNFa, IL-17A, IL-2, or IL-6 in the cell, tissue, or subject is increased by at least about 10%, at least about 20%, at least about 50%, at least about 75%, at least about 100%, at least about 150%, at least about 200%, at least about 250%, at least about 300%, at least about 400%, at least about 500%, at least about 600%, at least about 700%, at least about 800%, at least about 900%, or at least about 1,000%, relative to a similar or otherwise identical cell or tissue that has not been contacted with the fusion protein or antibody conjugate. Gene expression may be measured by any suitable method known in the art, for example, by ELISA, or by Luminex multiplex assays.

[00243] The invention also provides a method of promoting infiltration of immune cells into a tumor in a subject in need thereof. The method comprises administering to the subject an effective amount of a fusion protein and/or antibody conjugate, e.g, a fusion protein or antibody conjugate disclosed herein. In certain embodiments, the immune cells are T-cells, e.g, CD4+ and/or CD8+ T-cells, e.g., CD69 ⁺ CD8 ⁺ and/or GzmB ⁺ CD8 ⁺ T-cells. In certain embodiments, the immune cells are natural killer (NK) cells.

[00244] In certain embodiments, the infiltration of immune cells into the tumor in the subject is increased by at least about 10%, at least about 20%, at least about 50%, at least about 75%, at least about 100%, at least about 150%, at least about 200%, at least about 250%, at least about 300%, at least about 400%, at least about 500%, at least about 600%, at least about 700%, at least about 800%, at least about 900%, or at least about 1,000%, relative to a similar or otherwise identical tumor and/or subject that has not been administered the fusion protein or antibody conjugate. Infiltration of immune cells into a tumor may be measured by any suitable method known in the art, for example, antibody staining. [00245] The invention also provides a method of increasing the number of circulating natural killer (NK) cells in a subject in need thereof. The method comprises administering to the subject an effective amount of a fusion protein and/or antibody conjugate, e.g., a fusion protein or antibody conjugate disclosed herein, so as to increase the number of circulating NK cells relative to prior to administration of the fusion protein, antibody conjugate or pharmaceutical composition.

[00246] In certain embodiments, the number of circulating NK cells in the subject is increased by at least about 10%, at least about 20%, at least about 50%, at least about 75%, at least about 100%, at least about 150%, at least about 200%, at least about 250%, at least about 300%, at least about 400%, at least about 500%, at least about 600%, at least about 700%, at least about 800%, at least about 900%, or at least about 1,000%, relative to a similar or otherwise identical subject that has not been administered the fusion protein or antibody conjugate. Circulating NK cells in a subject may be measured by any suitable method known in the art, for example, antibody staining.

[00247] The invention also provides a method of increasing the number of T-cells in the draining lymph node in a subject in need thereof. The method comprises administering to the subject an effective amount of a fusion protein and/or antibody conjugate, e.g, a fusion protein or antibody conjugate disclosed herein, so as to increase the number of T-cells in the draining lymph node relative to prior to administration of the fusion protein, antibody conjugate or pharmaceutical composition. In certain embodiments, the immune cells are T-cells, e.g, CD4+ and/or CD8+ T-cells.

[00248] In certain embodiments, the number of T-cells in the draining lymph node in the subject is increased by at least about 10%, at least about 20%, at least about 50%, at least about 75%, at least about 100%, at least about 150%, at least about 200%, at least about 250%, at least about 300%, at least about 400%, at least about 500%, at least about 600%, at least about 700%, at least about 800%, at least about 900%, or at least about 1,000%, relative to a similar or otherwise identical subject that has not been administered the fusion protein or antibody conjugate. T-cells in the draining lymph node in a subject may be measured by any suitable method known in the art, for example, antibody staining.

[00249] The invention also provides a method of increasing expression of Cd3, Cd4, Cd8, Cd274, Ctla4, Icos, Pdcdl, Lag3, 116, II lb, 112, Ifing, Ifnal, Mxl, Gzmb, Cxcl9, Cxcll2, and/or Ccl5 in a cell, tissue, or subject. The method comprises contacting the cell, tissue, or subject with an effective amount of a fusion protein and/or antibody conjugate, e.g, a fusion protein or antibody conjugate disclosed herein, so as to increase the expression of Cd3, Cd4, Cd8, Cd274, Ctla4, Icos, Pdcdl, Lag3, 116, II lb, 112, Ifng, Ifnal, Mxl, Gzmb, Cxcl9, Cxcll2, and/or Ccl5 relative to the cell, tissue or subject prior to contact with the fusion protein, antibody conjugate or pharmaceutical composition.

[00250] In certain embodiments, expression of Cd3, Cd4, Cd8, Cd274, Ctla4, Icos, Pdcdl,

Lag3, 116, II lb, 112, Ifng, Ifnal, Mxl, Gzmb, Cxcl9, Cxcll2, and/or Ccl5 in the cell, tissue, or subject is increased by at least about 10%, at least about 20%, at least about 50%, at least about 75%, at least about 100%, at least about 150%, at least about 200%, at least about 250%, at least about 300%, at least about 400%, at least about 500%, at least about 600%, at least about 700%, at least about 800%, at least about 900%, or at least about 1,000%, relative to a similar or otherwise identical cell, tissue, or subject that has not been contacted with the fusion protein or antibody conjugate. Gene expression may be measured by any suitable method known in the art, for example, by ELISA, Luminex multiplex assays, or Nanostring technology.

[00251] The invention also provides a method of removing sialic acid from a cell or tissue. The method comprises contacting the cell or tissue with an effective amount of a fusion protein and/or antibody conjugate, e.g., a fusion protein or antibody conjugate disclosed herein. The invention also provides a method of removing sialic acid from a cell in a subject, the method comprising administering to the subject an effective amount of a pharmaceutical composition comprising a fusion protein and/or antibody conjugate, e.g, a fusion protein or antibody conjugate disclosed herein, thereby to remove sialic acid from the cell.

[00252] In certain embodiments, the cell is tumor cell, dendritic cell (DC) or monocyte. In certain embodiments, the cell is a monocyte, and the method results in increased expression of an MHC-II molecule (e.g., HLA-DR) on the monocyte. In certain embodiments, expression of an MHC-II molecule in the cell or tissue is increased by at least about 10%, at least about 20%, at least about 50%, at least about 75%, at least about 100%, at least about 150%, at least about 200%, at least about 250%, at least about 300%, at least about 400%, at least about 500%, at least about 600%, at least about 700%, at least about 800%, at least about 900%, or at least about 1,000%, relative to a similar or otherwise identical cell or tissue that has not been contacted with the fusion protein and/or antibody conjugate. Gene expression may be measured by any suitable method known in the art, for example, by ELISA, by Luminex multiplex assays, or by flow cytometry.

[00253] The invention also provides a method of enhancing phagocytosis of a tumor cell. The method comprises contacting the tumor cell with a fusion protein and/or antibody conjugate, e.g., a fusion protein or antibody conjugate disclosed herein, in an amount effective to remove sialic acid from the tumor cell, thereby enhancing phagocytosis of the tumor cell. In certain embodiments, the disclosure relates to a method of increasing phagocytosis of a tumor cell in a subject, the method comprising administering to the subject an effective amount of a

pharmaceutical composition a fusion protein and/or antibody conjugate, e.g, a fusion protein or antibody conjugate disclosed herein, in an amount effective to remove sialic acid from the tumor cell, thereby to increase phagocytosis of the tumor cell.

[00254] In certain embodiments, phagocytosis is increased by at least about 10%, at least about 20%, at least about 50%, at least about 75%, at least about 100%, at least about 150%, at least about 200%, at least about 250%, at least about 300%, at least about 400%, at least about 500%, at least about 600%, at least about 700%, at least about 800%, at least about 900%, or at least about 1,000%, relative to a similar or otherwise identical tumor cell or population of tumor cells that has not or have not been contacted with the fusion protein and/or antibody conjugate.

Phagocytosis may be measured by any suitable method known in the art.

[00255] The invention also provides a method of activating a dendritic cell (DC). The method comprises contacting the DC with a tumor cell that has been treated with a fusion protein and/or antibody conjugate, e.g, a fusion protein or antibody conjugate disclosed herein. In certain embodiments, the disclosure relates to a method of activating a dendritic cell (DC) or a population of DCs in a subject, the method comprising administering to the subject an amount of a pharmaceutical composition comprising a fusion protein and/or antibody conjugate, e.g., a fusion protein or antibody conjugate disclosed herein, effective to remove sialic acid from a tumor cell in the subject, thereby to activate the DC or the population of DCs in the subject.

[00256] In certain embodiments, activation of the DC or a population of DCs is increased by at least about 10%, at least about 20%, at least about 50%, at least about 75%, at least about 100%, at least about 150%, at least about 200%, at least about 250%, at least about 300%, at least about 400%, at least about 500%, at least about 600%, at least about 700%, at least about 800%, at least about 900%, or at least about 1,000%, relative to a similar or otherwise identical DC or population of DCs that has not or have not been contacted with a tumor cell that has been treated with the fusion protein and/or antibody conjugate. Activation may be measured by any suitable method known in the art.

[00257] The invention also provides a method of reducing Siglec-15 binding activity, thereby to increase anti -turn or activity in a tumor microenvironment, the method comprising contacting a T cell with a fusion protein and/or antibody conjugate, e.g, a fusion protein or antibody conjugate disclosed herein. In certain embodiments, the disclosure relates to a method of reducing Siglec-15 binding activity, thereby to increase anti -turn or activity in a tumor microenvironment of a patient, the method comprising administering to the subject an effective amount of a pharmaceutical composition comprising a fusion protein and/or antibody conjugate, e.g., a fusion protein or antibody conjugate disclosed herein, thereby to increase anti-tumor activity (e.g., T cell activity) in the subject.

[00258] In certain embodiments, Siglec-15 binding activity is reduced by at least about 10%, at least about 20%, at least about 50%, at least about 75%, or about 100%, relative to Siglec-15 that has not or have not been contacted with the fusion protein and/or antibody conjugate.

Binding may be measured by any suitable method known in the art.

[00259] Throughout the description, where compositions are described as having, including, or comprising specific components, or where processes and methods are described as having, including, or comprising specific steps, it is contemplated that, additionally, there are compositions of the present invention that consist essentially of, or consist of, the recited components, and that there are processes and methods according to the present invention that consist essentially of, or consist of, the recited processing steps.

[00260] In the application, where an element or component is said to be included in and/or selected from a list of recited elements or components, it should be understood that the element or component can be any one of the recited elements or components, or the element or component can be selected from a group consisting of two or more of the recited elements or components.

[00261] Further, it should be understood that elements and/or features of a composition or a method described herein can be combined in a variety of ways without departing from the spirit and scope of the present invention, whether explicit or implicit herein. For example, where reference is made to a particular compound, that compound can be used in various embodiments of compositions of the present invention and/or in methods of the present invention, unless otherwise understood from the context. In other words, within this application, embodiments have been described and depicted in a way that enables a clear and concise application to be written and drawn, but it is intended and will be appreciated that embodiments may be variously combined or separated without parting from the present teachings and invention(s). For example, it will be appreciated that all features described and depicted herein can be applicable to all aspects of the invention(s) described and depicted herein. [00262] It should be understood that the expression“at least one of’ includes individually each of the recited objects after the expression and the various combinations of two or more of the recited objects unless otherwise understood from the context and use. The expression“and/or” in connection with three or more recited objects should be understood to have the same meaning unless otherwise understood from the context.

[00263] The use of the term“include,”“includes,”“including,”“have,” “has,”“having,” “contain,”“contains,” or“containing,” including grammatical equivalents thereof, should be understood generally as open-ended and non-limiting, for example, not excluding additional unrecited elements or steps, unless otherwise specifically stated or understood from the context.

[00264] Where the use of the term“about” is before a quantitative value, the present invention also includes the specific quantitative value itself, unless specifically stated otherwise. As used herein, the term“about” refers to a ±10% variation from the nominal value unless otherwise indicated or inferred.

[00265] It should be understood that the order of steps or order for performing certain actions is immaterial so long as the present invention remain operable. Moreover, two or more steps or actions may be conducted simultaneously.

[00266] The use of any and all examples, or exemplary language herein, for example,“such as” or“including,” is intended merely to illustrate better the present invention and does not pose a limitation on the scope of the invention unless claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the present invention.

EXAMPLES

[00267] The following Examples are merely illustrative and are not intended to limit the scope or content of the invention in any way.

Example 1

[00268] This example describes the construction of recombinant human sialidases (Neul, Neu2, and Neu3).

[00269] The human sialidases Neul, Neu2, Neu3 (isoform 1), and Neu4 (isoform 1) were expressed as secreted proteins with a lOxHis tag. To express Neul as a secreted protein, the native N terminal signal peptide

(MTGERP ST ALPDRRW GPRILGF W GGCRVWVF AAIFLLLSL AAS W SKA; SEQ ID NO: 27) was replaced by MDMRVPAQLLGLLLLWLPGARC (SEQ ID NO: 28), and the C terminal lysosomal signal motif (YGTL; SEQ ID NO: 29) was removed. To express Neu2, Neu3, and Neu4 as secreted proteins, the N terminal signal peptide MDMRVPAQLLGLLLLWLPGARC (SEQ ID NO: 28) was added to each.

[00270] Sialidases were expressed in a 200 mL transfection of HEK293F human cells in 24- well plates using the pCEP4 mammalian expression vector with an N-terminal 6xHis tag.

Sialidases were purified using Ni-NTA columns, quantified with a UV-Vis spectrophotometer (NanoDrop), and examined by SDS-PAGE as shown in FIGURE 1. Neul expressed well, with a yield of ~3 pg/ml, and was present primarily in a monomeric form. Neu2 and Neu3 expression each gave yields of -0.15 pg/mL and each were present primarily in a dimeric form. Neu4 had no detectable expression yield as measured by NanoDrop. Bacterial sialidase from Salmonella typhimurium (St-sialidase; SEQ ID NO: 30), which was used as a positive control for expression, gave a comparable yield to Neul, and was present primarily in a monomeric form.

[00271] The activity of the recombinantly expressed sialidases was assayed by measuring the release of sialic acid from the fluorogenic substrate 4-methylumbelliferyl-N-acetylneuraminic acid (4MU-NeuAc). As shown in FIGURE 2, Neul has no detectable activity above a no enzyme control, which is consistent with previous reports indicating that Neul is inactive unless it is in complex with beta-galactosidase and protective protein/cathepsin A (PPCA). Neu2 and Neu3 were active. An enzyme kinetics assay was performed with Neu2 and Neu3. A fixed concentration of enzyme at 1 nM was incubated with fluorogenic substrate 4MU-NeuAc at concentrations ranging from 4000 mM to 7.8 pM. Assays were conducted at both acidic (pH 5.6) and neutral (pH 7) conditions. As shown in FIGURE 3, both Neu2 and Neu3 were active at acidic and neutral conditions and showed enzyme kinetics that were comparable to those previously reported.

[00272] Most of the recombinantly expressed sialidases ran as aggregates or dimers on a non reducing SDS-PAGE gel. Subsequent treatment with the reducing agent dithiothreitol (DTT) resulted in a monomeric form of the enzyme that ran at 42 kDa on a reducing SDS-PAGE gel (FIGURE 1)

Example 2

[00273] This example describes the construction of recombinant human sialidases with mutations that increase expression and/or activity of the sialidase.

A. Rational Design [00274] Structural and sequence analysis identified residues A93 and P62 of Neu2 as candidates for substitutions to increase solubility and/or expression. In particular, a comparison of homologous sialidase sequences showed a preference for D or E amino acid residues at positions corresponding to position 93 of Neu2, and a preference for G amino acid residues at positions corresponding to position 62 of Neu2.

[00275] The beta-propeller family of proteins are usually stabilized by extensive hydrogen bonding interactions at the N- and C-termini of the protein. A structural analysis revealed that Neu2, which is a member of the beta-propeller family, appears to lack these stabilizing interactions. In contrast, sialidases from Salmonella typhimurium and Micromonospora viridifaciens (the bacterial sialidase most homologous to human Neu2) have extensive hydrogen bonding interactions at their N- and C-termini. Accordingly, residues K9, V363, and L365 of Neu2 were mutated to promote hydrogen bonding between the N- and C-termini of Neu2.

B. Phase Display

[00276] Neu2 was expressed in a phage display system allowing for screening of Neu2 variants for both expression level and resistance to heat denaturation. Neu2 with V6Y and I187K substitutions was used as a template for library preparation. Designed phage display libraries 1, 2, and 3 are depicted in TABLEs 10-12, respectively. Each library included all of the possible combinations of the mutations depicted. A fourth library included random mutations generated by error prone PCR.

TABLE 10 - Phage Library 1

TABLE 11 - Phage Library 2

TABLE 12 - Phage Library 3 [00277] The codon usage columns in TABLES 10-12 represent degenerate codon codes used in the design of the library, where the first, second, and third positions of a given codon encoding an amino acid are as shown in TABLE 13 and as described in Mena et al. (2005) PROTEIN ENG DES SEL. 18(12):559-61.

TABLE 13

[00278] The phage display libraries were screened for binding to a conformation-specific antibody and/or a sialic acid biotinylated probe after heating to enrich for thermal stability and expression. The sialic acid biotinylated probe and its synthesis is depicted in FIGURE 4. An exemplary phage display screening procedure is depicted in FIGURE 5. Briefly, phage libraries expressing the desired Neu2 variants were generated. Phage were screened for binding to immobilized anti-Neu2 antibody and/or sialic acid biotinylated probe. Following washing to remove unbound phage, bound phage were eluted from the antibody or probe and analyzed as appropriate.

C. Yeast display

[00279] Neu2 was also expressed in a yeast display system allowing for screening of Neu2 variants for both expression level and resistance to heat denaturation. Neu2 with V6Y and I187K substitutions was used as a template for library preparation. Designed yeast display libraries la, lb, lc, Id, 2a, 2b, 2c, 3a, 3b, and 3c are depicted in TABLEs 14-23, respectively. Each library included all of the possible combinations of the mutations depicted. Five additional sublibraries were generated by error prone PCR, at an approximate average rate of 1, 2, 3, 4, and 5 substitutions per enzyme. TABLE 14 -Yeast Library la

Total Diversity: 2.30E+07

TABLE 15 - Yeast Library lb

Total Diversity: 4.11E+07

TABLE 16 -Yeast Library lc

Total Diversity: 4.53E+07 TABLE 17 -Yeast Library Id

Total Diversity: 4.30E+07

TABLE 18 -Yeast Library 2a

Total Diversity: 3.22E+08

TABLE 19 -Yeast Library 2b

Total Diversity: 3.22E+08

TABLE 20 -Yeast Library 2c

Total Diversity: 3.49E+09

TABLE 21 -Yeast Library 3a

Total Diversity: 3.63E+08 TABLE 22 -Yeast Library 3b

Total Diversity: 2.72E+08

TABLE 23 -Yeast Library 3c

Total Diversity: 2.72E+08

[00280] The codon usage columns in TABLES 14-23 represent degenerate codon codes used in the design of the library, where the first, second, and third positions of a given codon encoding an amino acid are as shown herein above in TABLE 13 and as described in Mena et al. (2005) PROTEIN ENG DES SEL. 18(12):559-61. [00281] The yeast display libraries were screened for binding to a conformation-specific antibody and/or a sialic acid biotinylated probe after heating to enrich for thermal stability and expression. An exemplary yeast display screening procedure is depicted in FIGURE 6. Briefly, a plasmid library encoding for the desired Neu2 variants, and yeast cells expressing the desired Neu2 variants on the surface, were generated. Yeast cells were heat shocked and then screened for binding to anti-Neu2 antibody and/or sialic acid biotinylated probe on magnetic beads. The magnetic beads were isolated to remove unbound cells, and bound cells were further analyzed for Neu2 affinity, activity, and stability as appropriate.

D. Results [00282] Mutant sialidases including mutations identified using the rational design, phage display, and yeast display approaches described in this Example were expressed as secreted proteins with a C-terminal human Fc tag in Expi293F cells using the pCEP4 mammalian expression vector. Expression was assayed using a ForteBio Octet with anti-human Fc sensors and Western blot and enzymatic activity was assayed using the fluorogenic substrate 4MU- NeuAc as described above.

[00283] Expression and activity levels for the mutant sialidases are shown in TABLE 24. In TABLE 24, enzymatic activity is indicated as“+++,” which denotes activity >2 fold higher than wild-type Neu2,“++,” which denotes activity comparable to wild-type Neu2,“+,” which denotes activity lower than wild-type Neu2, or which denotes no detectable activity, and expression is indicated as“++++,” which denotes expression > 15 fold higher than wildtype-Neu2,“+++,” which denotes expression > 6 fold higher than wild-type Neu2,“++,” which denotes expression 2-5 fold higher than wild-type Neu2,“+,” which denotes expression comparable to wild-type Neu2, or“-/’which denotes no detectable expression.

TABLE 24

[00284] To confirm these results, Neu2-M106 (with amino acid sequence SEQ ID NO: 48, encoded by nucleotide sequence SEQ ID NO: 80) was expressed and purified with a protein A column. FIGURE 7A is an image of an SDS-PAGE gel showing recombinant wildtype human Neu2 and Neu2 variant M106 (each with a C-terminal human Fc tag) under non-reducing and reducing conditions. FIGURE 7B is an SEC-HPLC trace for recombinant wildtype human Neu2 and Neu2 variant Ml 06 (each with a C-terminal human Fc tag). While Neu2-Fc had a yield of 0.3 mg/liter following protein-A purification, and monomer content of 7% as determined by SEC, Neu2-M106 had a yield of 20 mg/liter, and a monomer content of 85%. [00285] The enzyme kinetics of Neu2-M106 were assayed by measuring the release of sialic acid from the fluorogenic substrate 4-methylumbelliferyl-N-acetylneuraminic acid (4MU- NeuAc) as described above. A fixed concentration of enzyme at 2 pg/well was incubated with fluorogenic substrate 4MU-NeuAc at concentrations ranging from 4mM to 0.03 mM. FIGURE 8 depicts the enzyme activity of Neu2 variant M106. Enzymatic activity of Neu2-M106 was comparable to wildtype Neu2, with a KM determined to be 230mM. [00286] Together, these results show that the mutations identified by rational design, phage display, and/or yeast display approaches described herein can increase stability and/or expression of a sialidase.

Example 3

[00287] This example describes the construction of recombinant human sialidases with mutations that increase expression and/or activity of the sialidase.

[00288] Unless indicated otherwise, mutant sialidases in this Example were expressed as secreted proteins with a C-terminal human Fc tag in Expi293F cells using the pCEP4

mammalian expression vector. Expression was assayed using a ForteBio Octet with anti-human Fc sensors and Western blot and enzymatic activity was assayed using the fluorogenic substrate 4MU-NeuAc as described above.

[00289] Mutant Neu2 sialidases were constructed including rationally designed substitutions at position Q126. Inspection of the Neu2 crystal structure revealed that mutation of Q126 may increase interactions with neighboring amino acid residues.

[00290] Additional mutant Neu2 sialidases were constructed including rationally designed substitution at position Q270. Inspection of the Neu2 crystal structure revealed that mutation of Q270 to certain amino acids may stabilize interactions with R237 and stabilize binding in the substrate pocket.

[00291] Additional mutant Neu2 sialidases were constructed including a substitution of an amino acid residue in a beta turn with a proline (for example D80P, R189P, and/or H239P substitutions). Substitution with a proline at these positions may, for example, stabilize the protein by influencing local protein folding.

[00292] Expression and activity levels for the resulting mutant sialidases are shown in TABLE 25. In TABLE 25, enzymatic activity is indicated as“++,” which denotes activity comparable to wild-type Neu2,“+,” which denotes activity lower than wild-type Neu2, or which denotes no detectable activity, and expression is indicated as“+++++”, which denotes expression > 40 fold higher than wildtype-Neu2,“++++”, which denotes expression > 15 fold higher than wildtype-Neu2,“+++,” which denotes expression > 6 fold higher than wild-type Neu2,“++,” which denotes expression 2-5 fold higher than wild-type Neu2,“+,” which denotes expression comparable to wild-type Neu2, or“-,”which denotes no detectable expression. TABLE 25

[00293] To confirm these results, Neu2-M173 (with amino acid sequence SEQ ID NO: 100, encoded by nucleotide sequence SEQ ID NO: 118) was expressed with a C-terminal human Fc tag and purified with a protein A and a ceramic hydroxyapatite (CHT) column. FIGURE 9A is an image of an SDS-PAGE gel showing Neu2-M173-Fc (with a C-terminal human Fc tag) under non-reducing and reducing conditions. FIGURE 9B is an SEC-HPLC trace for Neu2-M173-Fc (with a C-terminal human Fc tag). Neu2-M173-Fc had a yield of 120 mg/liter, and a monomer content of 90%. [00294] The enzyme kinetics of Neu2-M173-Fc were assayed by measuring the release of sialic acid from the fluorogenic substrate 4-methylumbelliferyl-N-acetylneuraminic acid (4MU- NeuAc) as described above. A fixed concentration of enzyme at 2 pg/well was incubated with fluorogenic substrate 4MU-NeuAc at concentrations ranging from 4mM to 0.03 mM. FIGURE 10 depicts the enzyme activity of Neu2-M173-Fc. Enzymatic activity of Neu2-M173-Fc was comparable to wildtype Neu2, with a KM determined to be 230mM.

[00295] Additional mutant Neu2 sialidases were constructed including rationally designed substitutions at positions S301 and/or W302. Mutations of S301 and/or W302 may influence interactions with neighboring amino acid residues and/or substrate.

[00296] Expression and activity levels for the mutant sialidases are shown in TABLE 26. In

TABLE 26, enzymatic activity is indicated as“++,” which denotes activity comparable to wild- type Neu2,“+,” which denotes activity lower than wild-type Neu2, or which denotes no detectable activity, and expression is indicated as“+++++”, which denotes expression > 40 fold higher than wildtype-Neu2,“++++”, which denotes expression > 15 fold higher than wildtype- Neu2,“+++,” which denotes expression > 6 fold higher than wild-type Neu2,“++,” which denotes expression 2-5 fold higher than wild-type Neu2,“+,” which denotes expression comparable to wild-type Neu2, or“-/’which denotes no detectable expression.

TABLE 26

Example 4

[00297] This example describes the construction of recombinant human sialidases with mutations that reduce proteolytic cleavage.

[00298] Neu2-M106 (as described in Example 2, and with amino acid sequence SEQ ID

NO: 48) was expressed as an Fc-fused single chain protein using a CHO cell expression system in a large scale (10 L) high cell density production and purified with a protein A column. The resulting protein was analyzed by SDS-PAGE. Results are shown in FIGURE 11. Under reducing conditions, the protein included a mixture of full length (70 kDa, approx. 50%) and cleaved (40 kDa and 30 kDa, approx. 50%) fractions. However, in non-reducing conditions, there was no cleavage and the protein remained as a single chain (FIGURE 11). Additionally, when Neu2-M106 was expressed on a smaller scale (with a shorter duration of cell culture and lower cell density) there was no cleavage and the protein remained as a single chain. A preliminary mass spectrometry analysis showed that the 40 kDa and 30 kDa molecular weight fractions observed under reducing conditions following large scale production are a result of cleavage between amino acid residues R243 and V244 of the sialidase. The enzymatic activity of cleaved Neu2-M106 was similar to that of uncleaved Neu2-M106.

[00299] It was hypothesized that the cleavage of Neu2-M106 could be due to the activity of intracellular proteases released as a result of cell lysis during protein production, harvesting, and/or purification. To test this hypothesis, cleaved Neu2-M106 (prepared using the large scale- production described above that results in cleavage) and uncleaved Neu2-M106 (prepared using the smaller scale production described above that does not result in cleavage) were both incubated with trypsin and analyzed by SDS-PAGE under reducing conditions (FIGURE 12). Briefly, trypsin digestion reactions were performed by incubation of trypsin (5 pL, 0.005% solution in PBS) with Neu2-M106 (25 pL, 0.25 mg/mL in PBS pH 8.0) for 5 minutes on ice. Reactions were stopped by addition of LDS gel loading buffer (5 pL) and run on a reducing SDS-PAGE gel to observe trypsin mediated cleavage. The SDS-PAGE analysis showed that incubation of the uncleaved Neu2-M106 with trypsin resulted in the same cleavage pattern as that of the cleaved Neu2-M106. Additionally, incubation of the cleaved Neu2-M106 with trypsin resulted in increased intensity of the bands corresponding to the cleavage products.

[00300] Neu2-M106 was also incubated with trypsin in the presence of various protease inhibitors. Briefly, trypsin digestion reactions were performed by incubation of trypsin (0.005%) with Neu2-M106 (0.5 mg/mL) and protease inhibitor for 5 minutes on ice. Reactions were stopped by addition of LDS gel loading buffer and run on a reducing SDS-PAGE gel to observe trypsin mediated cleavage. Inhibitors used included iron citrate (at 0.3 and 5 mM), aprotinin (at 5,000 and 20,000 U/mL), AEBSF (at 0.1 and 1 mM), leupeptin (at 1 and 10 pM) or E-64 (at 1 and 10 pM). As seen in FIGURE 13, protease inhibitors reduced the extent of trypsin cleavage.

[00301] Together, these results confirm that cleavage of Neu2-M106 following large-scale production is due to trypsin or a member of a similar class of proteases.

[00302] We next attempted to rationally design recombinant human sialidases with mutations that increase resistance to trypsin cleavage.

[00303] Unless indicated otherwise, in the remainder of this Example mutant sialidases were expressed as secreted proteins with a C-terminal human Fc tag in Expi293F cells (on a 50 mL scale) using the pCEP4 mammalian expression vector. The resulting protein was purified using a Protein A column. Expression was assayed using a ForteBio Octet with anti-human Fc sensors and Western blot and enzymatic activity was assayed using the fluorogenic substrate 4MU-NeuAc as described above. Protease cleavage was assayed by SDS-PAGE as described above.

[00304] First, R243 was mutated to different polar/charged amino acids such as K, E, H,

N and Q. However, these mutations of R243 resulted in complete loss of activity and reduction in expression yields (R243 is also a conserved amino acid among similar sialidases).

[00305] Next, various amino residues surrounding the cleavage site were mutated and tested for expression, activity and trypsin cleavage resistance. Substitutions and combinations of substitutions that were tested are shown in FIGURE 14. All mutations were tested in a Neu2-

M106 background (i.e., including MID, V6Y, P62G, A93E, I187K, and C332A substitutions). [00306] Most of the mutant sialidases depicted in FIGURE 14 expressed well, however only two of the mutant sialidases (including V244I or A242C mutations) were active. The A242C mutation resulted in greater than 10 fold improved trypsin resistance and slightly lower activity (both relative to Neu2-M106). However, having an unpaired cysteine could be a potential liability, so, A242 was mutated to all 19 other amino acids and assayed for activity and trypsin resistance. As shown in FIGURE 15, mutation of A242 to aromatic amino acids such as F, W and Y resulted in a dramatic improvement in trypsin cleavage resistance compared to Neu2-M106 (FIGURE 15A) and similar enzymatic activity to Neu2-M106 (FIGURE 15B).

SEC analysis showed that proteins containing each of these mutations had a similar pattern to that of Neu2-M106 and more than 95% monomer content (FIGURE 15C).

[00307] Structural analysis showed that replacing A242 with an aromatic amino acid could provide additional hydrophobic or stacking interactions to L260 and V265 (nonpolar amino acids located in the vicinity of the A242). Therefore, L260 and V265 were also mutated to phenylalanine. Along with these mutations several other rationally designed mutants, which could provide extra stability, for example by increasing stacking interactions, were also tested for expression, activity, and protease resistance.

[00308] Select results are shown in FIGURE 16. As shown in FIGURE 16, the combination of R241 Y and A242F mutations (Neu2-M255) resulted in the most resistance to trypsin cleavage (a greater than 10 fold improved trypsin resistance relative to Neu2-M106).

[00309] Expression, activity, and protease resistance levels for the mutant sialidases are shown in TABLE 27. In TABLE 27, enzymatic activity is indicated as“++,” which denotes activity comparable to wild-type Neu2,“+,” which denotes activity lower than wild-type Neu2, or which denotes no detectable activity, and expression is indicated as“+++++”, which denotes expression > 40 fold higher than wildtype-Neu2,“++++”, which denotes expression >

15 fold higher than wildtype-Neu2,“+++,” which denotes expression > 6 fold higher than wild- type Neu2,“++,” which denotes expression 2-5 fold higher than wild-type Neu2,“+,” which denotes expression comparable to wild-type Neu2, or“-,”which denotes no detectable expression. Protease/trypsin resistance is indicated as“+++,” which denotes resistance > 10 fold higher than Neu2-M106;“++,” which denotes resistance > 5 fold higher than Neu2-M106,“+,” denotes resistance comparable to Neu2-M106, or which denotes resistance lower than Neu2- M106. NT = not tested.

TABLE 27

Example 5

[00310] This example describes the construction of an anti-PD-Ll antibody sialidase conjugate (ASC) based on the Janus format.

[00311] The architecture for four exemplary types of antibody sialidase conjugates (ASCs) is depicted in FIGURE 19. The first type of ASC, referred to as“Raptor,” includes an antibody (with two heavy chains and two light chains) with a sialidase fused at the C-terminus of each heavy chain of the antibody (FIGURE 19A). The second type of ASC, referred to as“Janus,” contains one antibody arm (with one heavy chain and one light chain), and one sialidase-Fc fusion with a sialidase fused at the N-terminus of one arm of the Fc. Each Fc domain polypeptide in the Janus ASC contains either the“knob” (T366Y) or“hole” (Y407T) mutation for heterodimerization (residue numbers according to EU numbering, Rabat, E.A., et al. (1991) supra) (FIGURE 19B). The third type of ASC, referred to as“Lobster,” contains two Fc domain polypeptides each with a sialidase fused at the N-terminus of the Fc and a scFv fused at the C-terminus of the Fc (FIGURE 19C). The fourth type of ASC, referred to as“Bunk,” contains one antibody arm (with one heavy chain and one light chain) with an scFv fused at the C-terminus of one arm of the Fc, and one sialidase-Fc fusion arm with a sialidase fused at the N- terminus of the other arm of the Fc. Each Fc domain polypeptide in the Bunk ASC contains either the“knob” (T366Y) or“hole” (Y407T) mutation for heterodimerization (residue numbers according to EU numbering, Kabat, E.A., et al. (1991) supra) (FIGURE 19D).

[00312] A Janus Antibody Sialidase Conjugate (ASC) was constructed using human Neu2 containing MID, V6Y, P62G, A93E, I187K, and C332A mutations and the variable region of avelumab, an anti-PD-Ll antibody. This Janus ASC (referred to as Janus #1, and including a first polypeptide chain with amino acid sequence SEQ ID NO: 64, encoded by nucleotide sequence SEQ ID NO: 76, a second polypeptide chain with amino acid sequence SEQ ID NO: 66, encoded by nucleotide sequence SEQ ID NO: 77, and a third polypeptide chain with amino acid sequence SEQ ID NO: 78, encoded by nucleotide sequence SEQ ID NO: 103) was expressed and characterized for purity using SDS-PAGE and enzymatic activity using 4MU- NeuAc as described below.

[00313] Janus #1 was expressed in a 600 mL transfection of Expi293 human cells using the pCEP4 mammalian expression vector. The ASC was purified using protein A followed by cation exchange chromatography, quantified with a UV-Vis spectrophotometer (NanoDrop), and examined by SDS-PAGE as shown in FIGURE 20. Janus #1 expressed with a yield of 34 mg with good purity after purification (see, e.g., FIGURE 21).

[00314] The activity of Janus #1 was assayed by measuring the release of sialic acid from the fluorogenic substrate 4-methylumbelliferyl-N-acetylneuraminic acid (4MU-NeuAc).

Specifically, an enzyme kinetics assay was performed by incubating a fixed concentration of enzyme at 1 nM with fluorogenic substrate 4MU-NeuAc at concentrations ranging from 4000 mM to 7.8 pM. As shown in FIGURE 22, Janus #1 was active, causing the release of sialic acid which generated fluorescence. Assays were conducted at pH 5.6.

[00315] FIGURE 23 shows a binding assay (ForteBio octet binding) between Avelumab (FIGURE 23A) or Janus #1 (FIGURE 23B) and recombinant human PD-L1. Janus #1 had a comparable Kd to Avelumab (1.28nM vs. 0.75 nM) as well as a comparable K _on (1.29 x 10 ⁵ vs. 3.31 x 10 ⁵ (1/Ms)) and K _dis (1 39 x 10 ⁴ vs. 2.35 10 ⁴ (1/s)) (FIGURE 23C).

Example 6

[00316] This example describes the construction of additional anti-PD-Ll antibody sialidase conjugates (ASCs) based on the Janus format, and the construction of anti-PD-Ll ASCs based on the Bunk and Lobster formats. [00317] A Janus ASC was constructed using Neu2 with MID, V6Y, P62G, A93E, I187K, and C332A mutations and the variable region of avelumab. This Janus ASC is referred to as Janus #2, and includes a first polypeptide chain with amino acid sequence SEQ ID NO: 64, encoded by nucleotide sequence SEQ ID NO: 76, a second polypeptide chain with amino acid sequence SEQ ID NO: 66, encoded by nucleotide sequence SEQ ID NO: 77, and a third polypeptide chain with amino acid sequence SEQ ID NO: 112, encoded by nucleotide sequence SEQ ID NO: 113.

Janus #2 has the same amino acid sequence as Janus #1 described in Example 5 except for a different linker sequence between the sialidase and Fc in the third polypeptide chain, where in Janus #1 the linker was GGGGS (SEQ ID NO: 121) and in Janus #2 the linker was

GGGGSGGGGS (SEQ ID NO: 90).

[00318] Another Janus ASC was constructed using a bacterial sialidase from Salmonella typhimurium (St-sialidase) and the variable region of avelumab. This Janus ASC is referred to as Janus #3, and includes a first polypeptide chain with amino acid sequence SEQ ID NO: 64, encoded by nucleotide sequence SEQ ID NO: 76, a second polypeptide chain with amino acid sequence SEQ ID NO: 66, encoded by nucleotide sequence SEQ ID NO: 77, and a third polypeptide chain with amino acid sequence SEQ ID NO: 106, encoded by nucleotide sequence SEQ ID NO: 107. Janus #3 also contains a C-terminal Histidine repeat sequence (His-tag) for potential purification.

[00319] Another Janus ASC was constructed using St-sialidase and the variable region of avelumab. This Janus ASC is referred to as Janus #4, and includes a first polypeptide chain with amino acid sequence SEQ ID NO: 64, encoded by nucleotide sequence SEQ ID NO: 76, a second polypeptide chain with amino acid sequence SEQ ID NO: 104, encoded by nucleotide sequence SEQ ID NO: 105, and a third polypeptide chain with amino acid sequence SEQ ID NO: 108, encoded by nucleotide sequence SEQ ID NO: 109. Janus #4 has an Asn297 to Gly (N297G) mutation in the Fc domain to remove an N-linked glycosylation site. Janus #4 also contains a C-terminal His-tag for potential purification.

[00320] A Bunk ASC was constructed using Neu2 with MID, V6Y, P62G, A93E, I187K, and C332A mutations, the variable region of avelumab, and an avelumab-based scFv. This Bunk ASC is referred to as Bunk #1, and includes a first polypeptide chain with amino acid sequence SEQ ID NO: 64, encoded by nucleotide sequence SEQ ID NO: 76, a second polypeptide chain with amino acid sequence SEQ ID NO: 110, encoded by nucleotide sequence SEQ ID NO: 111, and a third polypeptide chain with amino acid sequence SEQ ID NO: 78, encoded by nucleotide sequence SEQ ID NO: 103. [00321] Another Bunk ASC was constructed using St-sialidase, the variable region of avelumab, and an avelumab -based scFv. This Bunk ASC is referred to as Bunk #2, and includes a first polypeptide chain with amino acid sequence SEQ ID NO: 64, encoded by nucleotide sequence SEQ ID NO: 76, a second polypeptide chain with amino acid sequence SEQ ID NO: 110, encoded by nucleotide sequence SEQ ID NO: 111, and a third polypeptide chain with amino acid sequence SEQ ID NO: 106, encoded by nucleotide sequence SEQ ID NO: 107.

Bunk #2 also contains a C-terminal His-tag for potential purification.

[00322] A Lobster ASC was constructed using Neu2 with MID, V6Y, P62G, A93E, I187K, and C332A mutations and an avelumab-based scFv. This Lobster ASC is referred to as Lobster #1, and includes a first polypeptide with an amino acid sequence of SEQ ID NO: 114, encoded by nucleotide sequence SEQ ID NO: 115, and a second polypeptide with an amino acid sequence of SEQ ID NO: 114, encoded by nucleotide sequence SEQ ID NO: 115.

[00323] A depiction of each of the constructs described in this Example is shown in FIGURE 24

[00324] Janus #2, Janus #3, Janus #4, Bunk #1, Bunk #2, and Lobster #1 were each expressed in a 600 mL transfection of Expi293 human cells using the pCEP4 mammalian expression vector. The ASCs were purified using protein A followed by cation exchange chromatography, quantified with a UV-Vis spectrophotometer (NanoDrop), and examined by SDS-PAGE. Janus #1 was expressed and purified as described in Example 5, and Neu2-M106-Fc was expressed and purified as described in Example 2.

[00325] The activity of Janus #1, Janus #2, Bunk #1, Bunk #2, Lobster #1, and Neu2-M106-Fc was assayed by measuring the release of sialic acid from the fluorogenic substrate 4- methylumbelliferyl-N-acetylneuraminic acid (4MU-NeuAc). Specifically, an enzyme kinetics assay was performed by incubating a fixed concentration of enzyme at 1 nM with fluorogenic substrate 4MU-NeuAc at concentrations ranging from 2000 mM to 7.8 pM. As shown in

FIGURE 25, the tested ASCs were all active, causing the release of sialic acid which generated fluorescence.

[00326] Monomer purity of Janus #2, Janus #3, Bunk #2, and Lobster #1 was assayed by Size Exclusion Chromatography (SEC). As shown in FIGURE 26, the tested ASCs had a percent homogeneity ranging from 80 to 100%.

[00327] The binding kinetics of Janus #2, Janus #3, Bunk #1, Bunk #2, and Lobster #1 for recombinant human PD-L1 was determined by ForteBio octet binding. Avelumab was used as a control. Monovalent binding kinetics experiments, where the ASC was adsorbed onto the sensor and PD-L1 was titrated in, are shown in FIGURE 27. Avidity driven binding experiments, where PD-L1 was adsorbed onto the sensor and the ASC was titrated in, are shown in FIGURE 28. Kinetic parameters are shown in TABLE 28. As can be seen, all ASCs demonstrated comparable binding kinetics to aveulmab.

TABLE 28

Example 7

[00328] This example describes the testing of anti-PD-Ll antibody sialidase conjugates (ASCs) in a cell-based assay measuring the disruption of human PD-L1 binding to PD-1.

[00329] Janus #2, Janus #3, Bunk #1, Bunk #2, and Lobster #1 were expressed and purified as described in Example 6. The avelumab-based ASCs were tested in the PD-1/PD-L1 Blockade Bioassay (Promega, Cat. Nos. J1250 and J1255) according to manufacturer’s instructions. In brief, the avelumab-based ASCs were co-cultured with (i) engineered CHO-K1 cells expressing human PD-L1 and TCR activating protein and (ii) Jurkat T cells expressing human PD-1, TCR and a luciferase reporter driven by an NFAT response element. A schematic of the assay is depicted in FIGURE 29. Absent intervention, PD-L1 interacting with PD-1 inhibits TCR- mediated luminescence. Blockade of the PD-L1/ PD-1 interaction, for instance using avelumab or avelumab-based ASCs, results in a luminescent signal. A luciferase substrate was added after 6 hours of incubation and luminescence was measured. Relative light units (RLU) were calculated by subtracting background (substrate and media only) from assay wells. Fold induction was calculated by dividing RLU (induced minus background) by RLU (no antibody control minus background). As can be seen in FIGURE 30, the tested avelumab-based ASCs disrupted the PD-Ll/PD-1 interaction, resulting in a dose dependent increase in luminescence. EC50s of the ASCs were comparable to the EC50 for avelumab.

Example 8

[00330] This Example describes the in vivo administration of anti-PD-Ll antibody sialidase conjugates (ASCs) containing human sialidases. [00331] Avelumab-based Janus ASCs can be tested in a mouse syngeneic tumor model injected with a murine cancer cell line either expressing endogenous PD-L1 or engineered to express human PD-L1, as avelumab binds human and mouse PD-L1 with similar affinity.

Female BALB/c mice, 6-8 weeks of age, are inoculated subcutaneously in the right lower flank region with either the parent murine cell line or human PD-L1 expressing tumor cells for tumor development. Mice are randomly allocated to 4 groups of 5 animals each when tumors reach 50- 100 mm ³ , mean ~ 75-100 mm ³ .

[00332] Mice are treated via intraperitoneal injection of 10 mg/kg of either avelumab-based Janus ASC, avelumab, or vehicle control, and tumor volume (mm ³ ) is recorded. Mean tumor volumes for the individual mice for the indicated treatments are determined. Complete

Responses (CR, defined as regression below the limit of palpitation at any point during the study) are also determined.

[00333] It is expected that avelumab-based Janus ASC will reduce tumor volume and increase the number of CRs as compared to vehicle control. It is also expected that avelumab-based Janus ASC will reduce tumor volume comparably or better than avelumab.

Example 9

[00334] This example describes in vivo testing of avelumab-based ASCs in an A20 syngeneic mouse model. Mouse A20 cells express endogenous mouse PD-L1 which is bound by avelumab and avelumab-based ASCs. Female Balb/c mice, 5-6 weeks of age, were inoculated subcutaneously in the right lower flank region with murine A20 B cell lymphoma cells in matrigel (1 : 1 by volume). Mice were randomly allocated into groups of 8 mice when tumors reached approximately 100 mm ³ (the average tumor volume of each group ranged from 86 to 90 mm ³ ). TABLE 29 describes the various arms of the study. Mice were treated intraperitoneally with 1-30 mg/kg of Janus #3 (as described in Example 6), avelumab, or antibody isotype control twice a week for a total of 5 doses. Tumor volumes and body weights were recorded three times a week.

TABLE 29

[00335] FIGURE 31 depicts the tumor growth in each mouse in each of the groups. Complete responders (CR) and partial responders (PR) for each group are shown. As can be seen, Janus #3 demonstrated a dose dependent increase in PR and CR.

[00336] Mice with tumors that demonstrated CR were grouped and rechallenged with murine A20 cells (all approximately 12 weeks of age) and compared to naive control mice injected with A20 cells of either 6 or 12 weeks of age. Tumor volumes and body weights were recorded three times a week. While tumors grew as expected in both the 6 week and 12 week naive mice, no substantial tumor growth was observed in the rechallenged mice.

Example 10

[00337] This example describes in vivo testing of avelumab-based ASCs in an A20 syngeneic mouse model. Mouse A20 cells express endogenous mouse PD-L1 which is bound by avelumab and avelumab-based ASCs. Female Balb/c mice, 5-6 weeks of age, were inoculated subcutaneously in the right lower flank region with murine A20 B cell lymphoma cells in matrigel (1 : 1 by volume). Mice were randomly allocated into groups of 8 mice when tumors reached approximately 100 mm ³ (the average tumor volume of each group ranged from 84 to 92 mm ³ ). TABLE 30 describes the various arms of the study. Mice were treated intraperitoneally with 10-13.5 mg/kg Janus #2, Janus #3, Janus #4, Bunk #2, Lobster #1 (as described in Example 6), avelumab, or antibody isotype control twice a week for a total of 6 doses. Tumor volumes and body weights were recorded three times a week.

TABLE 30

[00338] FIGURE 32 depicts the results of tumor growth in each mouse in each of the groups. The avelumab-based ASCs demonstrated varying degrees of efficacy.

INCORPORATION BY REFERENCE

[00339] The entire disclosure of each of the patent and scientific documents referred to herein is incorporated by reference for all purposes.

EQUIVALENTS

[00340] The invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The foregoing embodiments are therefore to be considered in all respects illustrative rather than limiting on the invention described herein.

Scope of the invention is thus indicated by the appended claims rather than by the foregoing description, and all changes that come within the meaning and range of equivalency of the claims are intended to be embraced therein.

SEQUENCE LISTING

[00341] SEQ ID NO: 1 :

MASLPVLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPIQR PI P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSCAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00342] SEQ ID NO: 2:

MEDLRPMATCPVLQKETLFRTGVHAYRIPALLYLKKQKTLLAFAEKRASKTDEHAELIVL RRGS YNEATNRVKWQPEEWTQAQLEGHRSMNPCPLYDKQTKTLFLFFIAVPGRVSEHHQLHTKV NVT RLCCVSSTDHGRTWSPIQDLTETTIGSTHQEWATFAVGPGHCLQLRNPAGSLLVPAYAYR KLHP AQKPTPFAFCFISLDHGHTWKLGNFVAENSLECQVAEVGTGAQRMVYLNARSFLGARVQA QSPN DGLDFQDNRWSKLVEPPHGCHGSWAFHNPISKPHALDTWLLYTHPTDSRNRTNLGVYLNQ MP LDPTAWSEPTLLAMGICAYSDLQNMGQGPDGSPQFGCLYESGNYEEI I FLI FTLKQAFPTVFDA

Q

[00343] SEQ ID NO: 3 :

EDLRP

[00344] SEQ ID NO: 4:

MEDLRP

[00345] SEQ ID NO: 5:

DKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCWVDVSHEDPEVKFNWYVDG VEV

HNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQ PREPQV

YTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFF LYSKLTV

DKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00346] SEQ ID NO: 6:

ACAGTGGAAAAGTCCGTGGTGTTCAAGGCCGAGGGCGAGCACTTCACCGACCAGAAAGGC AATA CCATCGTCGGCTCTGGCAGCGGCGGCACCACCAAGTACTTTAGAATCCCCGCCATGTGCA CCAC CAGCAAGGGCACCATTGTGGTGTTCGCCGACGCCAGACACAACACCGCCAGCGATCAGAG CTTC ATCGATACCGCTGCCGCCAGATCTACCGATGGCGGCAAGACCTGGAACAAGAAGATCGCC ATCT ACAACGACCGCGTGAACAGCAAGCTGAGCAGAGTGATGGACCCTACCTGCATCGTGGCCA ACAT CCAGGGCAGAGAAACCATCCTGGTCATGGTCGGAAAGTGGAACAACAACGATAAGACCTG GGGC GCCTACAGAGACAAGGCCCCTGATACCGATTGGGACCTCGTGCTGTACAAGAGCACCGAT GACG GCGTGACCTTCAGCAAGGTGGAAACAAACATCCACGACATCGTGACCAAGAACGGCACCA TCTC TGCCATGCTCGGCGGCGTTGGATCTGGCCTGCAACTGAATGATGGCAAGCTGGTGTTCCC CGTG CAGATGGTCCGAACAAAGAATATCACCACCGTGCTGAATACCAGCTTCATCTACAGCACC GACG GCATCACATGGTCCCTGCCTAGCGGCTACTGTGAAGGCTTTGGCAGCGAGAACAACATCA TCGA GTTCAACGCCAGCCTGGTCAACAACATCCGGAACAGCGGCCTGCGGAGAAGCTTCGAGAC AAAG GACTTCGGAAAGACGTGGACCGAGTTTCCTCCAATGGACAAGAAGGTGGACAACCGGAAC CACG GCGTGCAGGGCAGCACAATCACAATCCCTAGCGGCAACAAACTGGTGGCCGCTCACTCTA GCGC CCAGAACAAGAACAACGACTACACCAGAAGCGACATCAGCCTGTACGCCCACAACCTGTA CAGC GGCGAAGTGAAGCTGATCGACGACTTCTACCCCAAAGTGGGCAATGCCAGCGGAGCCGGC TACA GCTGTCTGAGCTACCGGAAAAATGTGGACAAAGAAACCCTGTACGTGGTGTACGAGGCCA ACGG CAGCATCGAGTTTCAGGACCTGAGCAGACATCTGCCCGTGATCAAGAGCTACAAC

[00347] SEQ ID NO: 7:

ENDFGLVQPLVTMEQLLWVSGRQIGSVDTFRIPLITATPRGTLLAFAEARKMSSSDEGAK FIAL RRSMDQGSTWSPTAFIVNDGDVPDGLNLGAVVSDVETGVVFLFYSLCAHKAGCQVASTML VWSK DDGVSWSTPRNLSLDIGTEVFAPGPGSGIQKQREPRKGRLIVCGHGTLERDGVFCLLSDD HGAS WRYGSGVSGIPYGQPKQENDFNPDECQPYELPDGSWINARNQNNYHCHCRIVLRSYDACD TLR PRDVTFDPELVDPWAAGAWTSSGIVFFSNPAHPEFRVNLTLRWSFSNGTSWRKETVQLWP GP SGYSSLATLEGSMDGEEQAPQLYVLYEKGRNHYTES ISVAKISV

[00348] SEQ ID NO: 8:

MEEVTTCSFNSPLFRQEDDRGITYRIPALLYIPPTHTFLAFAEKRSTRRDEDALHLVLRR GLRI GQLVQWGPLKPLMEATLPGHRTMNPCPVWEQKSGCVFLFFICVRGHVTERQQIVSGRNAA RLCF IYSQDAGCSWSEVRDLTEEVIGSELKHWATFAVGPGHGIQLQSGRLVIPAYTYYIPSWFF CFQL PCKTRPHSLMIYSDDLGVTWHHGRLIRPMVTVECEVAEVTGRAGHPVLYCSARTPNRCRA EALS TDHGEGFQRLALSRQLCEPPHGCQGSWSFRPLEIPHRCQDSSSKDAPTIQQSSPGSSLRL EEE AGTPSESWLLYSHPTSRKQRVDLGIYLNQTPLEAACWSRPWILHCGPCGYSDLAALEEEG LFGC LFECGTKQECEQIAFRLFTHREILSHLQGDCTSPGRNPSQFKSN

[00349] SEQ ID NO: 9:

MRPADLPPRPMEESPASSSAPTETEEPGSSAEVMEEVTTCSFNSPLFRQEDDRGITYRI PALLY IPPTHTFLAFAEKRSTRRDEDALHLVLRRGLRIGQLVQWGPLKPLMEATLPGHRTMNPCP VWEQ KSGCVFLFFICVRGHVTERQQIVSGRNAARLCFIYSQDAGCSWSEVRDLTEEVIGSELKH WATF AVGPGHGIQLQSGRLVIPAYTYYIPSWFFCFQLPCKTRPHSLMIYSDDLGVTWHHGRLIR PMVT VECEVAEVTGRAGHPVLYCSARTPNRCRAEALSTDHGEGFQRLALSRQLCEPPHGCQGSW SFR PLEIPHRCQDSSSKDAPTIQQSSPGSSLRLEEEAGTPSESWLLYSHPTSRKQRVDLGIYL NQTP LEAACWSRPWILHCGPCGYSDLAALEEEGLFGCLFECGTKQECEQIAFRLFTHREILSHL QGDC TSPGRNPSQFKSN

[00350] SEQ ID NO: 10:

MGVPRTPSRTVLFERERTGLTYRVPSLLPVPPGPTLLAFVEQRLSPDDSHAHRLVLRRGT LAGG SVRWGALHVLGTAALAEHRSMNPCPVHDAGTGTVFLFFIAVLGHTPEAVQIATGRNAARL CCVA SRDAGLSWGSARDLTEEAIGGAVQDWATFAVGPGHGVQLPSGRLLVPAYTYRVDRRECFG KICR TSPHSFAFYSDDHGRTWRCGGLVPNLRSGECQLAAVDGGQAGSFLYCNARSPLGSRVQAL STDE GTSFLPAERVASLPETAWGCQGS IVGFPAPAPNRPRDDSWSVGPGSPLQPPLLGPGVHEPPEEA AVDPRGGQVPGGPFSRLQPRGDGPRQPGPRPGVSGDVGSWTLALPMPFAAPPQSPTWLLY SHPV GRRARLHMGIRLSQSPLDPRSWTEPWVIYEGPSGYSDLAS IGPAPEGGLVFACLYESGARTSYD E I S FCTFSLREVLENVPASPKPPNLGDKPRGCCWPS

[00351] SEQ ID NO: 11 :

MMSSAAFPRWLSMGVPRTPSRTVLFERERTGLTYRVPSLLPVPPGPTLLAFVEQRLSPDD SHAH

RLVLRRGTLAGGSVRWGALHVLGTAALAEHRSMNPCPVHDAGTGTVFLFFIAVLGHT PEAVQIA

TGRNAARLCCVASRDAGLSWGSARDLTEEAIGGAVQDWATFAVGPGHGVQLPSGRLL VPAYTYR VDRRECFGKICRTSPHSFAFYSDDHGRTWRCGGLVPNLRSGECQLAAVDGGQAGSFLYCN ARSP LGSRVQALSTDEGTSFLPAERVASLPETAWGCQGSIVGFPAPAPNRPRDDSWSVGPGSPL QPPL LGPGVHEPPEEAAVDPRGGQVPGGPFSRLQPRGDGPRQPGPRPGVSGDVGSWTLALPMPF AAPP QSPTWLLYSHPVGRRARLHMGIRLSQSPLDPRSWTEPWVIYEGPSGYSDLASIGPAPEGG LVFA CLYESGARTSYDEISFCTFSLREVLENVPASPKPPNLGDKPRGCCWPS

[00352] SEQ ID NO: 12:

MASLP

[00353] SEQ ID NO: 13 :

ASLP

[00354] SEQ ID NO: 14:

TVEKSWF

[00355] SEQ ID NO: 15:

GDYDAPTHQVQW

[00356] SEQ ID NO: 16:

SMDQGSTW

[00357] SEQ ID NO: 17:

STDGGKTW

[00358] SEQ ID NO: 18:

PRPPAPEA

[00359] SEQ ID NO: 19:

QTPLEAAC

[00360] SEQ ID NO: 20:

NPRPPAPEA

[00361] SEQ ID NO: 21 :

SQNDGES

[00362] SEQ ID NO: 22:

LSHSLST

[00363] SEQ ID NO: 23 : GAGAACGACTTTGGACTGGTGCAGCCTCTGGTCACCATGGAACAGCTGCTGTGGGTTTCC GGCA GACAGATCGGCAGCGTGGACACCTTCAGAATCCCTCTGATCACCGCCACACCTAGAGGCA CCCT GCTGGCCTTTGCCGAGGCCAGAAAGATGAGCAGCTCTGACGAGGGCGCCAAGTTTATTGC CCTG AGGCGGTCTATGGACCAGGGCTCTACATGGTCCCCTACCGCCTTCATCGTGAACGATGGC GACG TGCCCGATGGCCTGAATCTGGGAGCTGTGGTGTCCGATGTGGAAACCGGCGTGGTGTTCC TGTT CTACAGCCTGTGTGCCCACAAGGCCGGTTGTCAGGTGGCCAGCACAATGCTCGTGTGGTC CAAG GACGACGGCGTGTCCTGGTCTACCCCTAGAAACCTGAGCCTGGACATCGGCACCGAAGTG TTTG CTCCAGGACCTGGCTCTGGCATCCAGAAGCAGAGAGAGCCCAGAAAGGGCAGACTGATCG TGTG TGGCCACGGCACCCTTGAGAGAGATGGCGTTTTCTGCCTGCTGAGCGACGATCATGGCGC CTCT TGGAGATACGGCAGCGGAGTGTCTGGAATCCCTTACGGCCAGCCTAAGCAAGAGAACGAT TTCA ACCCCGACGAGTGCCAGCCTTACGAGCTGCCTGATGGCAGCGTCGTGATCAACGCCCGGA ACCA GAACAACTACCACTGCCACTGCCGGATCGTGCTGAGAAGCTACGACGCCTGCGATACCCT GCGG CCTAGAGATGTGACCTTCGATCCTGAGCTGGTGGACCCTGTTGTTGCCGCTGGTGCCGTC GTGA CATCTAGCGGCATCGTGTTCTTCAGCAACCCTGCTCACCCCGAGTTCAGAGTGAATCTGA CCCT GCGGTGGTCCTTCAGCAATGGCACAAGCTGGCGGAAAGAAACCGTGCAGCTTTGGCCTGG ACCT AGCGGCTACTCTTCTCTGGCTACACTGGAAGGCAGCATGGACGGCGAAGAACAGGCCCCT CAGC T G T AC G T G C T G T AC GAGAAGG G C AGAAAC C AC T AC AC C GAGAG CAT C AG C G T G G C C AAGAT C AG CGTT

[00364] SEQ ID NO: 24:

ATGGCCAGCCTGCCTGTGCTGCAGAAAGAAAGCGTGTTCCAGTCTGGCGCCCACGCCTAC AGAA TTCCCGCTCTGCTGTATCTGCCAGGCCAGCAGTCTCTGCTGGCTTTCGCTGAACAGCGGG CCAG C AAGAAG GAT GAG C AC G C C GAAC T GAT CGTGCTGCG GAGAG G C GAT T AC GAC G C C C C T AC AC AT CAGGTGCAGTGGCAGGCTCAAGAGGTGGTGGCTCAGGCTAGACTGGACGGCCACAGATCT ATGA ACCCCTGTCCTCTGTACGATGCCCAGACCGGCACACTGTTTCTGTTCTTTATCGCTATCC CCGG C C AAG T GAC C GAG C AG C AG C AG C T G C AG AC AAG AG C C AAC G T GAC C AG AC T G T G T C AAG T GAC C TCCACCGACCACGGCAGAACCTGGTCTAGCCCTAGAGATCTGACCGACGCCGCCATCGGA CCTG CCTATAGAGAGTGGTCCACCTTCGCCGTTGGACCTGGACACTGTCTCCAGCTGCACGACA GGGC TAGATCTCTGGTGGTGCCTGCCTACGCCTATAGAAAGCTGCACCCCATCCAGCGGCCTAT TCCT AGCGCCTTCTGCTTTCTGAGCCACGATCACGGCAGGACATGGGCCAGAGGACATTTCGTG GCCC AGGACACACTGGAATGCCAGGTGGCCGAAGTGGAAACCGGCGAGCAGAGAGTCGTGACCC TGAA C G C C AGAT C T C AC C T GAGAGC C AGAG T G C AG G C C C AGAG C AC AAAC GAC G G C C T G GAT T T C C AA GAGAGCCAGCTGGTCAAGAAACTGGTGGAACCTCCTCCACAGGGCTGTCAGGGAAGCGTG ATCA GCTTTCCATCTCCTAGAAGCGGCCCTGGCTCTCCTGCTCAGTGGCTGCTGTATACACACC CCAC ACACAGCTGGCAGAGAGCCGATCTGGGCGCCTACCTGAATCCTAGACCTCCTGCTCCTGA GGCT TGGAGCGAACCTGTTCTGCTGGCCAAGGGCAGCTGTGCCTACAGCGATCTGCAGTCTATG GGCA CAGGCCCTGATGGCAGCCCTCTGTTTGGCTGTCTGTACGAGGCCAACGACTACGAAGAGA TCGT GTTCCTGATGTTCACCCTGAAGCAGGCCTTTCCAGCCGAGTACCTGCCTCAA

[00365] SEQ ID NO: 25:

ATGGAGGAAGTGACCACCTGTAGCTTCAACAGCCCTCTGTTCCGGCAAGAGGACGACCGG GGCA TCACCTACAGAATCCCTGCTCTGCTGTACATCCCTCCTACACACACCTTTCTGGCCTTCG CCGA GAAG C G GAG C AC C AGAC GAGAT GAAGAT G C C C T G C AC CTGGTGCT GAGAAGAG G C C T GAGAAT C GGACAGCTGGTGCAGTGGGGACCTCTGAAGCCTCTGATGGAAGCCACACTGCCCGGCCAC AGAA CCATGAATCCTTGTCCTGTGTGGGAGCAGAAAAGCGGCTGCGTGTTCCTGTTCTTCATCT GCGT GCGGGGCCACGTGACCGAGAGACAGCAAATCGTGTCCGGCAGAAACGCCGCCAGACTGTG CTTC ATCTACAGCCAGGATGCCGGCTGCTCTTGGAGCGAAGTTCGGGATCTGACCGAAGAAGTG ATCG GCAGCGAGCTGAAGCACTGGGCCACATTTGCTGTTGGCCCTGGCCACGGAATCCAGCTGC AATC TGGCAGACTGGTCATCCCCGCCTACACCTACTATATCCCCAGCTGGTTCTTCTGCTTCCA ACTG CCTTGCAAGACCCGGCCTCACAGCCTGATGATCTACAGCGACGATCTGGGCGTGACATGG CACC ACGGCAGACTGATCAGACCCATGGTCACCGTGGAATGCGAGGTGGCCGAAGTGACAGGCA GAGC TGGACACCCTGTGCTGTACTGCTCTGCCAGAACACCCAACCGGTGTAGAGCCGAGGCTCT GTCT ACAGATCACGGCGAGGGCTTTCAGAGACTGGCCCTCTCTAGACAGCTGTGCGAACCTCCT CATG GCTGTCAGGGCAGCGTGGTGTCCTTCAGACCTCTGGAAATCCCTCACCGGTGCCAGGACA GCAG CTCTAAGGATGCCCCTACCATCCAGCAGTCTAGCCCTGGCAGCAGCCTGAGACTGGAAGA GGAA GCCGGAACACCTAGCGAGAGCTGGCTGCTGTACTCTCACCCCACCAGCAGAAAGCAGAGA GTGG ACCTGGGCATCTACCTGAATCAGACCCCTCTGGAAGCCGCCTGTTGGAGCAGACCTTGGA TTCT GCACTGTGGCCCTTGCGGCTACTCTGATCTGGCCGCTCTGGAAGAAGAGGGCCTGTTCGG CTGC CTGTTTGAGTGCGGCACAAAGCAAGAGTGCGAGCAGATCGCCTTCCGGCTGTTCACCCAC AGAG AGATCCTGAGCCATCTGCAGGGCGACTGCACAAGCCCAGGCAGAAATCCCAGCCAGTTCA AGAG CAAC

[00366] SEQ ID NO: 26:

ATGGGCGTGCCCAGAACACCCAGCAGAACCGTGCTGTTCGAGAGAGAGAGGACCGGCCTG ACCT

ACAGAGTGCCTTCTCTGCTGCCTGTGCCTCCTGGACCTACACTGCTGGCCTTCGTGG AACAGAG

ACTGAGCCCCGATGATTCTCACGCCCACAGACTGGTGCTGAGAAGAGGAACACTGGC TGGCGGC

TCTGTTAGATGGGGAGCACTGCATGTGCTGGGCACAGCTGCTCTTGCCGAGCACAGA TCCATGA

ATCCCTGTCCTGTGCACGACGCCGGAACCGGCACAGTGTTTCTGTTCTTTATCGCCG TGCTGGG

CCACACACCTGAGGCCGTTCAAATTGCCACCGGCAGAAATGCCGCCAGACTGTGTTG TGTGGCC

TCCAGAGATGCCGGCCTGTCTTGGGGATCTGCCAGAGATCTGACCGAGGAAGCCATT GGCGGAG

CCGTTCAGGATTGGGCCACATTTGCTGTTGGACCTGGACACGGCGTGCAGCTGCCAA GTGGTAG

ACTGCTGGTGCCTGCCTACACATACAGAGTGGATCGGAGAGAGTGCTTCGGAAAGAT CTGCCGG

ACAAGCCCTCACAGCTTCGCCTTCTACTCCGACGATCACGGCCGGACTTGGAGATGT GGTGGCC

TGGTGCCTAATCTGAGAAGCGGCGAATGTCAACTGGCCGCCGTTGATGGTGGACAGG CTGGCAG

CTTCCTGTACTGCAACGCCAGATCTCCTCTGGGCTCTAGAGTGCAGGCCCTGTCTAC CGATGAG

GGCACCAGTTTTCTGCCCGCCGAAAGAGTTGCCTCTCTGCCTGAAACAGCCTGGGGC TGTCAGG

GCTCTATCGTGGGATTTCCTGCTCCTGCTCCAAACAGACCCCGGGACGATTCTTGGA GTGTCGG

CCCTGGATCTCCACTGCAGCCTCCATTGCTTGGACCAGGCGTTCACGAGCCACCTGA AGAGGCT

GCCGTTGATCCTAGAGGCGGACAAGTTCCTGGCGGCCCTTTTAGCAGACTGCAGCCA AGAGGCG

ACGGCCCTAGACAACCTGGACCAAGACCTGGCGTCAGCGGAGATGTTGGCTCTTGGA CACTGGC

CCTGCCTATGCCTTTTGCCGCTCCTCCTCAGTCTCCTACCTGGCTGCTGTACTCTCA CCCTGTT

GGCAGACGGGCCAGACTGCACATGGGCATCAGACTGTCTCAGAGCCCTCTGGACCCC AGAAGCT

GGACAGAGCCTTGGGTCATCTATGAGGGCCCTAGCGGCTACAGCGATCTGGCCTCTA TTGGCCC

AGCTCCTGAAGGCGGACTGGTGTTCGCTTGTCTGTATGAGAGCGGCGCCAGAACCAG CTACGAC

GAGATCAGCTTCTGCACCTTCAGCCTGCGCGAGGTGCTGGAAAATGTGCCCGCCTCT CCTAAGC

CTCCTAACCTGGGCGATAAGCCTAGAGGCTGTTGCTGGCCATCT

[00367] SEQ ID NO: 27:

MTGERPSTALPDRRWGPRILGFWGGCRVWVFAAI FLLLSLAASWSKA

[00368] SEQ ID NO: 28:

MDMRVPAQLLGLLLLWLPGARC [00369] SEQ ID NO: 29:

YGTL

[00370] SEQ ID NO: 30:

MTVEKSWFKAEGEHFTDQKGNTIVGSGSGGTTKYFRIPAMCTTSKGTIWFADARHNTASD QS FIDTAAARSTDGGKTWNKKIAIYNDRVNSKLSRVMDPTCIVANIQGRETILVMVGKWNNN DKTW GAYRDKAPDTDWDLVLYKSTDDGVTFSKVETNIHDIVTKNGTISAMLGGVGSGLQLNDGK LVFP VQMVRTKNITTVLNTSFIYSTDGITWSLPSGYCEGFGSENNI IEFNASLVNNIRNSGLRRSFET KDFGKTWTEFPPMDKKVDNRNHGVQGST I T I PSGNKLVAAHSSAQNKNNDYTRSDI SLYAHNLY SGEVKLIDDFYPKVGNASGAGYSCLSYRKNVDKETLYWYEANGSIEFQDLSRHLPVIKSY N

[00371] SEQ ID NO: 31 :

EPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFN WYV

DGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTIS KAKGQP

REPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDS DGSFFLY

SKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00372] SEQ ID NO: 32:

DKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVDG VEV

HNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQ PREPQV

YTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFF LTSKLTV

DKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00373] SEQ ID NO: 33 :

EPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFN WYV

DGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTIS KAKGQP

REPQVYTLPPSREEMTKNQVSLYCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDS DGSFFLY

SKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00374] SEQ ID NO: 34:

ATGAGACCTGCGGACCTGCCCCCGCGCCCCATGGAAGAATCCCCGGCGTCCAGCTCTGCC CCGA CAGAGACGGAGGAGCCGGGGTCCAGTGCAGAGGTCATGGAAGAAGTGACAACATGCTCCT TCAA CAGCCCTCTGTTCCGGCAGGAAGATGACAGAGGGATTACCTACCGGATCCCAGCCCTGCT CTAC ATACCCCCCACCCACACCTTCCTGGCCTTTGCAGAGAAGCGTTCTACGAGGAGAGATGAG GATG CTCTCCACCTGGTGCTGAGGCGAGGGTTGAGGATTGGGCAGTTGGTACAGTGGGGGCCCC TGAA GCCACTGATGGAAGCCACACTACCGGGGCATCGGACCATGAACCCCTGTCCTGTATGGGA GCAG AAGAGTGGTTGTGTGTTCCTGTTCTTCATCTGTGTGCGGGGCCATGTCACAGAGCGTCAA CAGA TTGTGTCAGGCAGGAATGCTGCCCGCCTTTGCTTCATCTACAGTCAGGATGCTGGATGTT CATG GAGTGAGGTGAGGGACTTGACTGAGGAGGTCATTGGCTCAGAGCTGAAGCACTGGGCCAC ATTT GCTGTGGGCCCAGGTCATGGCATCCAGCTGCAGTCAGGGAGACTGGTCATCCCTGCGTAT ACCT ACTACATCCCTTCCTGGTTCTTTTGCTTCCAGCTACCATGTAAAACCAGGCCTCATTCTC TGAT GATCTACAGTGATGACCTAGGGGTCACATGGCACCATGGTAGACTCATTAGGCCCATGGT TACA GTAGAATGTGAAGTGGCAGAGGTGACTGGGAGGGCTGGCCACCCTGTGCTATATTGCAGT GCCC GGACACCAAACAGGTGCCGGGCAGAGGCGCTCAGCACTGACCATGGTGAAGGCTTTCAGA GACT GGCCCTGAGTCGACAGCTCTGTGAGCCCCCACATGGTTGCCAAGGGAGTGTGGTAAGTTT CCGG CCCCTGGAGATCCCACATAGGTGCCAGGACTCTAGCAGCAAAGATGCACCCACCATTCAG CAGA GCTCTCCAGGCAGTTCACTGAGGCTGGAGGAGGAAGCTGGAACACCGTCAGAATCATGGC TCTT GTACTCACACCCAACCAGTAGGAAACAGAGGGTTGACCTAGGTATCTATCTCAACCAGAC CCCC TTGGAGGCTGCCTGCTGGTCCCGCCCCTGGATCTTGCACTGTGGGCCCTGTGGCTACTCT GATC TGGCTGCTCTGGAGGAGGAGGGCTTGTTTGGGTGTTTGTTTGAATGTGGGACCAAGCAAG AGTG TGAGCAGATTGCCTTCCGCCTGTTTACACACCGGGAGATCCTGAGTCACCTGCAGGGGGA CTGC ACCAGCCCTGGTAGGAACCCAAGCCAATTCAAAAGCAAT

[00375] SEQ ID NO: 35:

ATGATGAGCTCTGCAGCCTTCCCAAGGTGGCTGAGCATGGGGGTCCCTCGTACCCCTTCA CGGA

CAGTGCTCTTCGAGCGGGAGAGGACGGGCCTGACCTACCGCGTGCCCTCGCTGCTCC CCGTGCC

CCCCGGGCCCACCCTGCTGGCCTTTGTGGAGCAGCGGCTCAGCCCTGACGACTCCCA CGCCCAC

CGCCTGGTGCTGAGGAGGGGCACGCTGGCCGGGGGCTCCGTGCGGTGGGGTGCCCTG CACGTGC

TGGGGACAGCAGCCCTGGCGGAGCACCGGTCCATGAACCCCTGCCCTGTGCACGATG CTGGCAC

GGGCACCGTCTTCCTCTTCTTCATCGCGGTGCTGGGCCACACGCCTGAGGCCGTGCA GATCGCC

ACGGGAAGGAACGCCGCGCGCCTCTGCTGTGTGGCCAGCCGTGACGCCGGCCTCTCG TGGGGCA

GCGCCCGGGACCTCACCGAGGAGGCCATCGGTGGTGCCGTGCAGGACTGGGCCACAT TCGCTGT

GGGTCCCGGCCACGGTGTGCAGCTGCCCTCAGGCCGCCTGCTGGTACCCGCCTACAC CTACCGC

GTGGACCGCCGAGAGTGTTTTGGCAAGATCTGCCGGACCAGCCCTCACTCCTTCGCC TTCTACA

GCGATGACCACGGCCGCACCTGGCGCTGTGGAGGCCTCGTGCCCAACCTGCGCTCAG GCGAGTG

CCAGCTGGCAGCGGTGGACGGTGGGCAGGCCGGCAGCTTCCTCTACTGCAATGCCCG GAGCCCA

CTGGGCAGCCGTGTGCAGGCGCTCAGCACTGACGAGGGCACCTCCTTCCTGCCCGCA GAGCGCG

TGGCTTCCCTGCCCGAGACTGCCTGGGGCTGCCAGGGCAGCATCGTGGGCTTCCCAG CCCCCGC

CCCCAACAGGCCACGGGATGACAGTTGGTCAGTGGGCCCCGGGAGTCCCCTCCAGCC TCCACTC

CTCGGTCCTGGAGTCCACGAACCCCCAGAGGAGGCTGCTGTAGACCCCCGTGGAGGC CAGGTGC

CTGGTGGGCCCTTCAGCCGTCTGCAGCCTCGGGGGGATGGCCCCAGGCAGCCTGGCC CCAGGCC

TGGGGTCAGTGGGGATGTGGGGTCCTGGACCCTGGCACTCCCCATGCCCTTTGCTGC CCCGCCC

CAGAGCCCCACGTGGCTGCTGTACTCCCACCCAGTGGGGCGCAGGGCTCGGCTACAC ATGGGTA

TCCGCCTGAGCCAGTCCCCGCTGGACCCGCGCAGCTGGACAGAGCCCTGGGTGATCT ACGAGGG

CCCCAGCGGCTACTCCGACCTGGCGTCCATCGGGCCGGCCCCTGAGGGGGGCCTGGT TTTTGCC

TGCCTGTACGAGAGCGGGGCCAGGACCTCCTATGATGAGATTTCCTTTTGTACATTC TCCCTGC

GTGAGGTCCTGGAGAACGTGCCCGCCAGCCCCAAACCGCCCAACCTTGGGGACAAGC CTCGGGG

GTGCTGCTGGCCCTCC

[00376] SEQ ID NO: 36:

MRFKNVKKTALMLAMFGMATSSNAALFDYNATGDTEFDSPAKQGWMQDNTNNGSGVLTNA DGMP AWLVQGIGGRAQWTYSLSTNQHAQASSFGWRMTTEMKVLSGGMITNYYANGTQRVLPI ISLDSS GNLWEFEGQTGRTVLATGTAATEYHKFELVFLPGSNPSAS FYFDGKLIRDNIQPTASKQNMIV WGNGSSNTDGVAAYRDIKFEIQGDVI FRGPDRIPS IVASSVTPGWTAFAEKRVGGGDPGALSN TNDI ITRTSRDGGITWDTELNLTEQINVSDEFDFSDPRPIYDPSSNTVLVSYARWPTDAAQNGD RIKPWMPNGI FYSVYDVASGNWQAPIDVTDQVKERSFQIAGWGGSELYRRNTSLNSQQDWQSNA KIRIVDGAANQIQVADGSRKYWTLS IDESGGLVANLNGVSAPI ILQSEHAKVHSFHDYELQYS ALNHTTTLFVDGQQITTWAGEVSQENNIQFGNADAQIDGRLHVQKIVLTQQGHNLVEFDA FYLA QQTPEVEKDLEKLGWTKIKTGNTMSLYGNASVNPGPGHGITLTRQQNISGSQNGRLIYPA IVLD RFFLNVMS IYSDDGGSNWQTGSTLPIPFRWKSSS ILETLEPSEADMVELQNGDLLLTARLDFNQ IVNGVNYSPRQQFLSKDGGITWSLLEANNANVFSNISTGTVDAS ITRFEQSDGSHFLLFTNPQG NPAGTNGRQNLGLWFSFDEGVTWKGPIQLVNGASAYSDIYQLDSENAIVIVETDNSNMRI LRMP ITLLKQKLTLSQN [00377] SEQ ID NO: 37:

TTGTCAATCAAGATGACTTCACAACGAAGAAGAGCATCGATTCACAAGGAAACAGATTCT AATA TAAAGGGAGTAGATATGCGTTTCAAAAACGTAAAGAAAACCGCTTTAATGCTTGCAATGT TCGG TATGGCGACAAGCTCAAACGCCGCACTTTTTGACTATAACGCAACGGGTGACACTGAGTT TGAC AGTCCAGCCAAACAGGGATGGATGCAAGACAACACGAATAATGGCAGCGGCGTTTTAACC AATG CAGATGGAATGCCCGCTTGGTTGGTGCAAGGTATTGGAGGGAGAGCTCAATGGACATATT CTCT CTCTACTAATCAACATGCCCAAGCATCAAGTTTCGGTTGGCGAATGACGACAGAAATGAA AGTG CTCAGTGGTGGAATGATCACAAACTACTACGCCAACGGCACTCAGCGTGTCTTACCCATC ATTT CATTAGATAGCAGTGGTAACTTAGTTGTTGAGTTTGAAGGGCAAACTGGACGCACCGTTT TGGC AACCGGCACAGCAGCAACGGAATATCATAAATTTGAATTGGTATTCCTTCCTGGAAGTAA CCCA TCCGCTAGCTTTTACTTCGATGGCAAACTCATTCGTGACAACATCCAGCCGACTGCATCA AAAC AAAATATGATCGTATGGGGGAATGGCTCATCAAATACGGATGGTGTCGCCGCTTATCGTG ATAT TAAGTTTGAAATTCAAGGCGACGTCATCTTCAGAGGCCCAGACCGTATACCGTCCATTGT AGCA AGTAGCGTAACACCAGGGGTGGTAACCGCATTTGCAGAGAAACGTGTGGGGGGAGGAGAT CCCG GTGCTCTGAGTAATACCAATGACATAATCACTCGTACCTCACGAGATGGCGGTATAACTT GGGA TACCGAGCTCAACCTCACTGAGCAAATCAATGTCAGTGATGAGTTTGATTTCTCCGATCC TCGG CCTATCTATGATCCTTCCTCCAATACGGTTCTTGTCTCTTATGCTCGATGGCCGACCGAT GCCG CTCAAAACGGAGATCGAATAAAACCATGGATGCCAAACGGTATTTTTTACAGCGTCTATG ATGT TGCATCAGGGAACTGGCAAGCGCCTATCGATGTTACCGATCAGGTGAAAGAACGCAGTTT CCAA ATCGCTGGTTGGGGTGGTTCAGAGCTGTATCGCCGAAATACCAGCCTAAATAGCCAGCAA GACT GGCAATCAAACGCTAAGATCCGAATTGTTGATGGTGCAGCGAACCAGATACAAGTTGCCG ATGG TAGCCGAAAATATGTTGTCACACTGAGTATTGATGAATCAGGTGGTCTAGTCGCTAATCT AAAC GGTGTTAGTGCTCCGATTATCCTGCAATCTGAACACGCAAAGGTACACTCTTTCCATGAC TACG AACTTCAATATTCGGCGTTAAACCACACCACAACGTTATTCGTGGATGGTCAGCAAATCA CAAC TTGGGCTGGCGAAGTATCGCAGGAGAACAACATTCAGTTTGGTAATGCGGATGCCCAAAT TGAC GGCAGACTGCATGTGCAAAAAATTGTTCTCACACAGCAAGGCCATAACCTCGTGGAGTTT GATG CTTTCTATTTAGCACAGCAAACCCCTGAAGTAGAGAAAGACCTTGAAAAGCTTGGTTGGA CAAA AATTAAAACGGGCAACACCATGAGTTTGTATGGAAATGCCAGTGTCAACCCAGGACCGGG TCAT GGCATCACCCTTACTCGACAACAAAATATCAGTGGCAGCCAAAACGGCCGCTTGATCTAC CCAG CGATTGTGCTTGATCGTTTCTTCTTGAACGTCATGTCTATTTACAGTGATGATGGCGGTT CAAA CTGGCAAACCGGTTCAACACTCCCTATCCCCTTTCGCTGGAAGAGTTCGAGTATCCTAGA AACT CTCGAACCTAGTGAAGCTGATATGGTTGAACTCCAAAACGGTGATCTACTCCTTACTGCA CGCC TTGATTTTAACCAAATCGTTAATGGTGTGAACTATAGCCCACGCCAGCAATTTTTGAGTA AAGA TGGTGGAATCACGTGGAGCCTACTTGAGGCTAACAACGCTAACGTCTTTAGCAATATCAG TACT GGTACCGTTGATGCTTCTATTACTCGGTTCGAGCAAAGTGACGGTAGCCATTTCTTACTC TTTA CTAACCCACAAGGAAACCCTGCGGGGACAAATGGCAGGCAAAATCTAGGCTTATGGTTTA GCTT CGATGAAGGGGTGACATGGAAAGGACCAATTCAACTTGTTAATGGTGCATCGGCATATTC TGAT ATTTATCAATTGGATTCGGAAAATGCGATTGTCATTGTTGAAACGGATAATTCAAATATG CGAA TTCTTCGTATGCCTATCACATTGCTAAAACAGAAGCTGACCTTATCGCAAAACTAA

[00378] SEQ ID NO: 38:

MVGADPTRPRGPLSYWAGRRGQGLAAI FLLLVSAAESEARAEDDFSLVQPLVTMEQLLWVSGKQ IGSVDTFRIPLITATPRGTLLAFAEARKKSASDEGAKFIAMRRSTDQGSTWSSTAFIVDD GEAS DGLNLGAVVNDVDTGIVFLIYTLCAHKVNCQVASTMLVWSKDDGISWSPPRNLSVDIGTE MFAP GPGSGIQKQREPGKGRLIVCGHGTLERDGVFCLLSDDHGASWHYGTGVSGIPFGQPKHDH DFNP DECQPYELPDGSVI INARNQNNYHCRCRIVLRSYDACDTLRPRDVTFDPELVDPWAAGALATS SGIVFFSNPAHPEFRVNLTLRWSFSNGTSWLKERVQVWPGPSGYSSLTALENSTDGKKQP PQLF VLYEKGLNRYTES I SMVKI SVYGTL [00379] SEQ ID NO: 39:

MTVQPSPWFSDLRPMATCPVLQKETLFRTGVHAYRIPALLYLKKQKTLLAFAEKRASKTD EHAE LIVLRRGSYNEATNRVKWQPEEWTQAQLEGHRSMNPCPLYDKQTKTLFLFFIAVPGRVSE HHQ LHTKVNVTRLCCVSSTDHGRTWSPIQDLTETTIGSTHQEWATFAVGPGHCLQLRNPAGSL LVPA YAYRKLHPAQKPTPFAFCFISLDHGHTWKLGNFVAENSLECQVAEVGTGAQRMVYLNARS FLGA RVQAQSPNDGLDFQDNRWSKLVEPPHGCHGSWAFHNPISKPHALDTWLLYTHPTDSRNRT NL GVYLNQMPLDPTAWSEPTLLAMGICAYSDLQNMGQGPDGSPQFGCLYESGNYEEI IFLIFTLKQ AFPTVFDAQ

[00380] SEQ ID NO: 40:

MEEVPPYSLSSTLFQQEEQSGVTYRIPALLYLPPTHTFLAFAEKRTSVRDEDAACLVLRR GLMK GRSVQWGPQRLLMEATLPGHRTMNPCPVWEKNTGRVYLFFICVRGHVTERCQIVWGKNAA RLCF LCSEDAGCSWGEVKDLTEEVIGSEVKRWATFAVGPGHGIQLHSGRLI IPAYAYYVSRWFLCFAC SVKPHSLMIYSDDFGVTWHHGKFIEPQVTGECQVAEVAGTAGNPVLYCSARTPSRFRAEA FSTD SGGCFQKPTLNPQLHEPRTGCQGSWSFRPLKMPNTYQDSIGKGAPATQKCPLLDSPLEVE KGA ETPSATWLLYSHPTSKRKRINLGIYYNRNPLEVNCWSRPWILNRGPSGYSDLAWEEQDLV ACL FECGEKNEYERIDFCLFSDHEVLSCEDCTSPSSD

[00381] SEQ ID NO: 41 :

METAGAPFCFHVDSLVPCSYWKVMGPTRVPRRTVLFQRERTGLTYRVPALLCVPPRPTLL AFAE QRLSPDDSHAHRLVLRRGTLTRGSVRWGTLSVLETAVLEEHRSMNPCPVLDEHSGTIFLF FIAV LGHTPEAVQIATGKNAARLCCVTSCDAGLTWGSVRDLTEEAIGAALQDWATFAVGPGHGV QLRS GRLLVPAYTYHVDRRECFGKICWTSPHSLAFYSDDHGISWHCGGLVPNLRSGECQLAAVD GDFL YCNARSPLGNRVQALSADEGTSFLPGELVPTLAETARGCQGSIVGFLAPPSIEPQDDRWT GSPR NTPHSPCFNLRVQESSGEGARGLLERWMPRLPLCYPQSRSPENHGLEPGSDGDKTSWTPE CPMS SDSMLQSPTWLLYSHPAGRRARLHMGIYLSRSPLDPHSWTEPWVIYEGPSGYSDLAFLGP MPGA SLVFACLFESGTRTSYEDISFCLFSLADVLENVPTGLEMLSLRDKAQGHCWPS

[00382] SEQ ID NO: 42:

GGGTCACATGCTGATGGACTAATTGGAGTCGCGGCAGCGCGGGCTGCGGCCCCCAAGGGG AGGG

GTCGGAGTGACGTGCGCGCTTTTAAAGGGCCGAGGTCAGCTGACGGCTTGCCACCGG TGACCAG

TTCCTGGACAGGGATCGCCGGGAGCTATGGTGGGGGCAGACCCGACCAGACCCCGGG GACCGCT

GAGCTATTGGGCGGGCCGTCGGGGTCAGGGGCTCGCAGCGATCTTCCTGCTCCTGGT GTCCGCG

GCGGAATCCGAGGCCAGGGCAGAGGATGACTTCAGCCTGGTGCAGCCGCTGGTGACC ATGGAGC

AGCTGCTGTGGGTGAGCGGGAAGCAGATCGGCTCTGTAGACACTTTCCGCATCCCGC TCATCAC

AGCCACCCCTCGGGGCACGCTCCTGGCCTTCGCTGAGGCCAGGAAAAAATCTGCATC CGATGAG

GGGGCCAAGTTCATCGCCATGAGGAGGTCCACGGACCAGGGTAGCACGTGGTCCTCT ACAGCCT

TCATCGTAGACGATGGGGAGGCCTCCGATGGCCTGAACCTGGGCGCTGTGGTGAACG ATGTAGA

CACAGGGATAGTGTTCCTTATCTATACCCTCTGTGCTCACAAGGTCAACTGCCAGGT GGCCTCT

ACCATGTTGGTTTGGAGTAAGGACGACGGCATTTCCTGGAGCCCACCCCGGAATCTC TCTGTGG

ATATTGGCACAGAGATGTTTGCCCCTGGACCTGGCTCAGGCATTCAGAAACAGCGGG AGCCTGG

GAAGGGCCGGCTCATTGTGTGTGGACACGGGACGCTGGAGCGAGATGGGGTCTTCTG TCTCCTC

AGTGATGACCACGGTGCCTCCTGGCACTACGGCACTGGAGTGAGCGGCATTCCCTTT GGCCAGC

CCAAACACGATCACGATTTCAACCCCGACGAGTGCCAGCCCTACGAGCTTCCAGATG GCTCGGT

CATCATCAACGCCCGGAACCAGAATAACTACCATTGCCGCTGCAGGATCGTCCTCCG CAGCTAT

GACGCCTGTGACACCCTCAGGCCCCGGGATGTGACCTTCGACCCTGAGCTCGTGGAC CCTGTGG

TAGCTGCAGGAGCACTAGCCACCAGCTCCGGCATTGTCTTCTTCTCCAATCCAGCCC ACCCTGA

GTTCCGAGTGAACCTGACCCTGCGCTGGAGTTTCAGCAATGGTACATCCTGGCAGAA GGAGAGG GTCCAGGTGTGGCCGGGACCCAGCGGCTACTCGTCCCTGACAGCCCTGGAAAACAGCACG GATG GAAAGAAGCAGCCCCCGCAGCTGTTCGTTCTGTACGAGAAAGGCCTGAACCGGTACACCG AGAG CATCTCCATGGTCAAAATCAGCGTCTACGGCACGCTCTGAGCCCCGTGCCCAAAGGACAC CAAG TCCTGGTCGCTGACTTCACAGCTCTCTGGACCATCTGCAGAGGGTGCCTGAAACACAGCT CTTC CTCTGAACTCTGACCTTTTGCAACTTCTCATCAACAGGGAAGTCTCTTCGTTATGACTTA ACAC CCAGCTTCCTCTCGGGGCAGGAAGTCCCTCCGTCACCAAGAGCACTTTTTTCCAGTATGC TGGG GATGGCCCCTGTCCATTCTCTTCCAGGACAACGGAGCTGTGCCTTTCTGGGACAGGATGG GGGA GGGGCTCCCCCTGGAGAGATGAACAGATACGAACTCAGGGAACTGAGAAGGCCCGGTGTC CTAG GGTACAAAGGCAGGTACTAGATGTGATTGCTGAAAGTCCCCAGGGCAGAGTGTCCTTTCA GAGC AAG GAT AAG C AC AC CTACGTGTG C AC CTTTGATTATTTAT GAAT C GAAAT AT T T G T AAC T T AAA ATTTTTGATGCAGAAAAAGCGTTTGTGGAGTCTGTGGTTCTGTCTGCTCACGCCTTCCCA ATTG C C T C C T G GAGAGAC AG GAAGG C AG C T G GAAGAG GAG C C GAT G T AC T T AC T G G GAAG C AGAAAC C CCTAGATTCCATCCTGGCTGCTGCTGTTTGCAAGTGTCAAAGATGGGGGGGCGTGTTTAT ATTT TATATTTC T AAGAT G G G G T GG C AT AG GAAAT AG G GAAC AGAT G T G T AAAAC C AGAT G G GAAG GA CAGTCTGTGAGAAAGGAGCAAGCAGTTGCTGCAGGTGTGGGAGAGCAAAGCCCTTCTCCA CGTG GAAAGAGCCCAGATGGACGCTAAGCATGTTGGGCACCTGTAACCCCGCACTCGCTGGACT GACG GTGTAGCTCAGTGGTGGAGCTAGTACTTGGAACGCCTAAGACTCTGGGTTCAGTCCTTGG GGGG GGGGGTATGTGTTTATTGAGAGGAAGGTGTACGTACTGTAGGTCAGAGGACAGCTTACTG GAGT TGTCTCTCTCCTTCACGCTGTGAGTCCTGTGGAATGACCTCAGGTGTCAGAGTTGGGGGC AGGT GCCTTTGCCAGCTGAGCCATCTTGCTGTCTCTGCTTTAATTTAAAAAAAAAAAAAAAAAA GAAT ATTAAGGTCTGAGGGATTCGGGCTGCGTTCATTTCAATTAGAGGGTCATATTTCTTTTGA CATT TCTTCTCTAAGAAATGTTAAGATCATTTGTTCTGTGTGATAGAGGTATAGCTCCATTGTA TGTC AGCAGTGAGGGATCCTGTGCATTTTATCCAGAGTTTGTACGGTGTTCTAGGGGCTGCTAG TGCA G C C C AG T G C T AAAC AC T T C AG CAT G C AC AAG G C C T C AAT C AG T G CAT G CAT G T G C AC AC AC AC A C AGAC AC AC AC G T AC AC AC T GAC AC AG G T AC AC AAAT AC AC AC T G G C C C AC AT G T AC AC AT C GA C T C AC AG G T AC AC AGAC C CAC T T T GACACACAT AT ACACAGACACAAAC GCAC T GGCACACACA TAT AC AC AG G C AC AC AT G GAT AGAT G GAC AC AC G T G T AC AC AT AC AC AC AC AC AC AGAAAT AC A AAT G T T C AG G T T T T C T AAAAAAAAAAAAAT T AGAGAC G T G T T GAC T T C AT T T T T AG C AAAAAT C CTGTCATGTATCTTAAAGTGGATTGAACCCACTATGTAGCCCAGGCTGGCCTCCAAATGG GCAT CCTTCTGCCTCAGTCTCCCGAGGGCTAGGATAACAGGAGTATGCCATCACACCTGGCTAA TAGA AATTTTCAAAATTGTTTGTTTGAAGGTGACTCTTACTATATTGCCTAACTGATCTCCAGT TCGT GAAAT CCTCCTGCCT C AGAAC C AG GAC T G T C AAT AT AAC C CAC C AAGAC AG G C C AAC AT T CAC A ATTGATTGTTAGTTTGTGGTCTGAATCAAGGTCTTATACTGTAGCCCAGGCTAGCCCGGA ATAC ACGATATCTCCAGTGCTTCAGATCCTCAGTTCTAACTAAGCATGGCCACATCCATGTTTA ACTG CAAATTTGATGTTACCATGGTTTGGTTTGGTTTGGTTTGGTTTGGTTTGGTTTGGTTTGG TTTT TTGGCCATTTTTTTTTTCTCATGCTGAGGCCTTGTGCTCTCAAGTTGGGGAGACAGCATG GAGG GTAGCTGCAACTGTAACCCCAGTTCCAGGGGACCTGACACCCTCTGGCCTCCACAAGTAT TAGG CACAT C T G T G G T G C AC AGACAT AC AAT C AG G C AAAAT AT T CATACACATAAAATAAAATAAT T T AAAAC AAAAG C AAAAAT CAGGAC C TAAGAAAAAAAT C TAT T C C T GAT T C T T T TAT G T T T T G T T T GTATTTTATCAAGACAGGGTTGTTTCTCTGTATAGCCCTGGCTGTCTTGGAATTCACTCT GTAG ACCAGGCTGGCCTCAAACTCAGAAATCCTCCTGCCTTTGCCTTCCAAGTGCTGGAATTAA AGGC ATGCGCCACC

[00383] SEQ ID NO: 43:

GACATGACCCAAACGGCCCCTGGCTGCAAGGTAATATCGGAAGTTGACTAAGAATGG ACGCCCC ACCACTGACTGACCCGCCCCCTGAGTCTGAGATTGGACTTGTCTCTGGATACAGTCATAC TTTG AG G T AC T AC AAG T T AGAAAC TGTTAGGTTACT C AG T T C AG T C C AT GAC AG T C C AAC C T T C T C C A TGGTTTTCCGATCTCAGGCCCATGGCGACCTGCCCTGTCCTGCAGAAGGAGACACTGTTC CGCA CAGGCGTCCATGCTTACAGAATCCCTGCTCTGCTCTACCTGAAGAAGCAGAAGACCCTGC TGGC C T T T G C G GAAAAG C GAG C C AG C AAGAC G GAT GAG CAC G C AGAG T T GAT T G T C C T GAGAAGAG GA AGCTACAACGAAGCCACCAACCGTGTCAAGTGGCAGCCTGAGGAAGTGGTGACCCAAGCC CAGC TGGAAGGCCACCGCTCCATGAATCCATGTCCCTTGTATGACAAGCAAACAAAGACCCTCT TCCT TTTCTTCATCGCTGTCCCTGGGCGTGTATCAGAACATCATCAGCTCCACACTAAGGTTAA TGTC ACACGGCTGTGCTGTGTCAGCAGCACTGACCATGGGAGGACCTGGAGCCCCATCCAGGAC CTCA CAGAGACCACCATTGGCAGCACTCATCAGGAATGGGCCACATTTGCTGTGGGTCCTGGGC ATTG TCTGCAGCTGCGGAACCCAGCTGGGAGCCTGCTGGTACCTGCTTATGCCTACCGGAAACT GCAC CCTGCTCAGAAGCCTACCCCCTTTGCCTTCTGCTTCATCAGCCTTGACCATGGGCACACA TGGA AACTAGGCAACTTTGTGGCTGAAAACTCACTGGAGTGCCAGGTGGCTGAGGTTGGCACTG GAGC TCAGAGGATGGTATATCTCAATGCTAGGAGCTTCCTGGGAGCCAGGGTCCAGGCACAAAG TCCT AATGATGGTCTGGATTTCCAGGACAACCGGGTAGTGAGTAAGCTTGTAGAGCCCCCCCAC GGGT GTCATGGAAGTGTGGTTGCCTTCCACAACCCCATCTCTAAGCCACATGCCTTAGACACAT GGCT T C T T TAT AC AC AC C C T AC AGAC T C C AG GAAT AGAAC C AAC CTGGGTGTGTACC TAAAC C AGAT G CCACTAGATCCCACAGCCTGGTCAGAGCCCACCCTGCTGGCCATGGGCATCTGTGCCTAC TCAG ACTTACAGAACATGGGGCAAGGCCCTGATGGCTCCCCACAGTTTGGGTGTCTGTATGAAT CAGG T AAC T AT GAAGAGAT C AT T T T C C T C AT AT T C AC C C T GAAG C AAG C T T T C C C C AC T G T AT T T GAT GCCCAGTGATCTCAGTGCACGTGGCCCAAAGGGCTTCCTTGTGCTTCAAAACACCCATCT CTCT TTGCTTCCAGCATCCTCTGGACTCTTGAGTCCAGCTCTTGGGTAACTTCCTCAGGAGGAT GCAG AGAATTTGGTCTCTTGACTCTCTGCAGGCCTTATTGTTTCAGCCTCTGGTTCTCTTTTCA GCCC AGAAATCAAAGGAGCCTGGCTTTCCTCAGCCTGTTGGCAGGGCAGGTGGGGACAGTATAT ATAG AGGCTGCCATTCTGCATGTCGGTTGTCACTATGCTAGTTTAACCTGCCTGTTTCCCCATG CCTA G T G T T T GAAT GAG T AT T AAT AAAAT AT C C AAC C C AG C C C AT T T C T T C C T G GAAAAAAA

[00384] SEQ ID NO: 44:

ACTGCGCGGTGAAGGGGCGTGGCCTGGCCGGGGAGGTTGACACCCAGACGCTGCTCT CAGTCCT CTGGCGCCTGCTCCCCAGCGCATTCCTTCTGCTCCTGGGATATTTGTCTCATTACTGCCA GTTC TTGCGCAGCGGTCACTGGGTTCGTTTCAGCGTCTGTGGTTTCTGTCGCTGTTATCCAGTC TCCA TCGCCCCAGCTCAGCTTCAGGCCTTCTTCCGAGACTCCACGGGAGAGCCCAGAGAGCCTC CGGA GCCGAAGCCATGGAGGAAGTCCCACCCTACTCCCTCAGCAGCACCCTGTTCCAGCAGGAA GAAC AGAGTGGGGTGACCTACCGGATCCCAGCCCTGCTGTACCTTCCTCCCACCCACACCTTCC TGGC CTTTGCAGAGAAGCGGACCTCAGTCAGAGATGAGGATGCTGCCTGCCTGGTGCTCAGACG AGGG CTGATGAAGGGGCGCTCTGTACAGTGGGGCCCCCAACGGCTACTGATGGAGGCCACATTA CCTG GGCATCGCACCATGAACCCCTGCCCTGTGTGGGAGAAAAATACTGGCCGTGTGTACCTGT TTTT CATCTGTGTGCGGGGCCATGTTACTGAGAGGTGCCAGATTGTGTGGGGCAAAAATGCCGC CCGT CTCTGCTTCCTTTGCAGTGAAGATGCCGGCTGCTCTTGGGGTGAAGTGAAAGACTTGACC GAGG AGGTCATTGGCTCAGAGGTGAAGCGCTGGGCCACATTTGCTGTGGGCCCAGGTCATGGCA TCCA GCTACACTCGGGAAGGCTGATCATCCCCGCCTATGCCTACTATGTCTCACGTTGGTTTCT CTGC TTTGCGTGTTCAGTCAAGCCCCATTCCCTGATGATCTACAGTGATGACTTTGGAGTCACA TGGC ACCATGGCAAGTTCATTGAGCCCCAGGTGACAGGGGAGTGCCAAGTGGCCGAAGTGGCTG GGAC GGCTGGTAACCCTGTGCTCACTGCAGTGCCCGAACACCAAGCCGATTTCGAGCAGAGGCT TTTA GTACTGATAGTGGTGGCTGCTTTCAGAAGCCAACCCTGAACCCACAACTCCATGAGCCTC GAAC CGGCTGCCAAGGTAGTGTAGTGAGCTTCCGGCCTTTGAAGATGCCAAATACCTATCAAGA CTCA ATTGGCAAAGGTGCTCCCGCTACTCAGAAGTGCCCTCTGCTGGACAGTCCTCTGGAGGTG GAGA AAG GAG CT GAAAC AC CAT C AG C AAC AT G G C T C T TGTAC T CACAT CCAAC TAG C AAGAG GAAGAG GATTAACCTAGGCATCTACTACAACCGGAACCCCTTGGAGGTGAACTGCTGGTCCCGCCC GTGG ATCTTGAACCGTGGGCCCAGTGGCTACTCTGATCTGGCTGTTGTGGAAGAACAGGACTTG GTGG CGTGTTTGTTTGAGTGTGGGGAGAAGAATGAGTATGAGCGGATTGACTTCTGTCTGTTTT CAGA CCATGAGGTCCTGAGCTGTGAAGACTGTACCAGCCCTAGTAGCGACTAAAGCCAAATCAA GACG GAT GAG T GAG G C C C AG C T T C C C AC AGAAAG GAAT G G C AG C T AC AG C C AG G G T AAC AGAG G T C T C TGATGTCTAGAGAAAACTCTAAAAACTAATAATCTGCTCCTTGAATTTTTTCACTTTTCC CTTC AATGAGCATGGTGAAAATTGTGCCATATCTTACATAACGAGGCTCTTGAACTGGGAGTTT GAAT CTCTTCTCTTCCCATTAAAAGGAGAGGCCATGTGCTCGCTTCGCGTTCGACAAAGCCTGG ATTC TGATCTTGAGTGGAAGCCACAGGCTTGTCTTTTCCAATGGTTCACTGCTCACCTGAGTAT TAGG TGATGTGTAGGTGCCTTGGCCAGAAGAAAGATCTGTGTTGTTGTATTTTTTTAAATTTAT TTAT T T AC TAT AT G T AAG T AC AC T G C AG C T G T C T T C AGAC AC AC C AGAAGAG G G C G T C AGAT C T CAT T AGAGATGGTTGTGAGCCACCATGTGGTTGCTGGGATTTGAACTCAGGACCTTCAGAAGAG CAGT C AG T G C T C T T AAC T AC T GAGC C AT C T C T C AAG C C C C G C AT T G C T G T AT T T T T AAT AAGAAAAAT GCCCTTATCCTTCCAATAATGCCTGGAGCTGTACAAATTCTCTGTCTTAGAAGACTTGAG AAAG CAGAACTGTAAGGTCAGATGCTTTCTCCAGCCTTGATGCTGTGTTCCACCTTCCCTTCCT CATC C AGAAAAC AG T T AC TAG G GAGAAAAT GAGAAAC C CAT G C C AG CTGCCCTT GAT GAT G G T T GAT A ACGGTGCTTATTGCTTTTGATGTCATTACCTCTGTTAGAGATGAATCAGAGTCAGAGGTC CTTA G C T G CAT C C AC C CAT T T C C AG G G G GAC AT T C T AAC AC T G C T GAAC AG T C AG C T AAAAT GAGAG C TGTGTGTCCTAGCCTGATTCCAGGTTAGTCATGATGCTTCCTGGAGCTGGGCTTTTATCT AATC CCAGGAGCCATCTAGGGGAGGCTCAGAGCTAGCAGGTGATCTTCCTGAGATGGTTTCACC GTGA C AG G T GAAC CAT GAG C C C T T C C AAG C AAG G C C AAAG GAC AAC AT TAT AG GAAAGAT T T C TAG T A TTAATATGCCTTTTCTCTGTGTGTGTACTGTCTTGTAGTGATGCTATATAGACAAATAGA TGAT TTCTTATTTTTTGTTTGTTTGTTTGTTTTTTTGTTTTTCTGTAGCCCTAGCTGTCCTGGA ACTC ACTTTGTAAACCAGGCTGGCCTCGATCTCAGAAATCCGCCTGCCTCTGCCTCCCGAGTGC TGGG AT T AAAG G T G T G C AC C AC C AC AC C T T AAT GAT GAT C C TAT AAG T AT T C C T AAAAT TAT AC TAG T AAT TAT T AAC T C C T T TAT AAT AG GAC T G C T AT T AAAG CCCTCGCTGATAT GAAAAC T AC AG T GA GAAC T C TGCCAGTC T T CACAT GT CAT AAT TAC T T C T GAGAT AGAAAG C AG G CAT T TACAAC T TA GAACACAT T T C T TAGAGC T GTAAAACAAT TAAC TAGAGGT CATAAAAGGGAAT GAAAGAT T TAT T G TAG G T G C TAG GAC AGAACAT AAAAT AT T GAC TGGGCT TAT C TAT AT GAAAC T T CAT T GT TAA C T T T TACACAAGAAT TAT GGT T T T TAAC T T T CAGT GAAC C T GCGGAGC TAG T GACAGAAGAGAA ATGTCTAGTTAGATAACTACTCTTAATGGAAATTCACATAAACATCTGTTGCCATCTTCT TTTT GAAT T T AT G T T TAAAC T T G T GAAT G T T T GAAT T AGAC AC T AC G C GAG CACAT AGAAAAT AAAGA ACTAAGCGTGAA

[00385] SEQ ID NO: 45:

GGACAGTGTGCATCACGGAGCTTGTGGCCCAGACTGTGCCTGGCAGACCCAGAGGAC CTAAGGC

TTGGCTCTAGTGGTGGTCAGCACAGCCCTCGGTGGTCTGCGGAGCCTGATATTGCTT TACGTAA

GGGCTGTTCTGCTGTGCATCTCCTGTGTCTGAAGCTATTCGCCATGGAGACTGCTGG AGCTCCC

TTCTGCTTCCATGTGGACTCCCTGGTACCTTGCTCCTACTGGAAGGTTATGGGGCCC ACGCGTG

TTCCCAGGAGAACGGTGCTCTTCCAGAGGGAAAGGACGGGCCTGACCTACCGTGTGC CTGCGTT

ACTCTGTGTGCCTCCCAGGCCTACTCTGCTGGCCTTCGCGGAACAGCGACTTAGCCC TGATGAC

TCCCATGCCCACCGCCTGGTGCTACGGAGGGGCACGCTGACCAGGGGCTCAGTGCGG TGGGGCA

CTCTGAGTGTACTGGAGACTGCAGTACTGGAGGAGCACAGGTCTATGAACCCTTGCC CGGTGCT

GGATGAGCACTCTGGTACCATCTTCCTCTTCTTCATTGCCGTGCTGGGCCACACACC GGAGGCC

GTGCAAATCGCCACTGGCAAGAACGCTGCTCGCCTCTGCTGTGTGACCAGCTGTGAC GCTGGCC

TCACCTGGGGCAGTGTTCGAGATCTCACTGAGGAAGCCATTGGTGCTGCATTGCAGG ACTGGGC

CACCTTTGCTGTGGGTCCGGGCCATGGAGTTCAGCTGCGCTCGGGTCGCCTGCTTGT TCCTGCT

TACACCTATCATGTGGACCGACGGGAATGTTTTGGCAAGATCTGCTGGACCAGTCCC CACTCCT

TGGCATTCTACAGTGATGATCATGGGATCTCCTGGCATTGTGGAGGCCTTGTGCCCA ACCTACG

CTCTGGAGAGTGCCAACTGGCTGCGGTAGATGGAGACTTTCTCTACTGTAATGCTCG AAGCCCT

CTGGGTAACCGTGTGCAGGCACTGAGTGCTGATGAAGGCACGTCCTTCCTACCAGGG GAGCTGG

TGCCTACATTGGCAGAGACGGCTCGTGGTTGCCAGGGTAGCATTGTGGGCTTCCTAG CTCCACC

CTCAATCGAGCCTCAGGATGACCGGTGGACAGGGAGTCCTAGGAACACCCCACATTC CCCATGC

TTCAATCTCAGAGTACAGGAGTCTTCGGGGGAAGGTGCCAGAGGTCTTCTTGAACGT TGGATGC

CCAGGTTGCCTCTCTGCTACCCACAGTCCCGGAGCCCAGAGAATCATGGCCTAGAGC CTGGGTC

AGATGGAGATAAGACATCCTGGACTCCGGAATGTCCTATGTCCTCTGATTCCATGCT TCAGAGC

CCCACATGGCTACTATATTCCCACCCAGCAGGGCGTAGAGCTCGGCTCCACATGGGA ATCTACC

TGAGCCGATCCCCCTTGGATCCCCACAGCTGGACAGAGCCCTGGGTGATCTATGAGG GCCCCAG

TGGCTACTCTGACCTTGCCTTTCTTGGGCCTATGCCTGGGGCATCCCTGGTTTTTGC CTGTCTG

TTTGAGAGCGGGACCAGGACTTCCTATGAAGACATTTCTTTTTGCTTGTTCTCACTG GCGGATG TCCTGGAGAATGTGCCCACTGGCTTAGAGATGCTAAGTCTCAGGGATAAGGCTCAGGGGC ATTG CTGGCCCTCTTGATGGCCTCACCCTCTCGTAGCCGCCTGGAGAGGAAGGGTAGACTATAT AGAG GAGGTTAGGGGTAGGTCAGCATGATGCTAGGATGGAGAGAGCTCTGTCCCCTCGTGGATG GTGG TGGTGACTCACCCGGGGGGCCAGCTGCTTTCTGAGTGCAAATGAGAAAAATAAAGAGCTG CGCT GTGACTTTTCTTTCCACATCAAAGCTTGGGTGTCAGTGCTTTAGCTTGATGCTCTGATCA CCAT GCAAATCTTCCACCGGCGCCTTGCTCAGCTTTCATATCCCAAGGGTGCCTGGGAGGAAGG CAAC AGGGACAGTGGACATCACTGCACCACTTTCCACGACCCTGTGTGCCAACCTCAGCCACTT TGAA ACATGCTGATGACTGAGGTCTGTTCACTTTCTTAATTTCAAGCAGGAGAAGCAGGTTGGG GAGC CAGCCTCCCCAGCTAGAGGGGACAGAACTTGACTTGAGCAGGGGGGTACCTCCTAGGACC TGCT CCATGTGCCTACTTCTTTACCCTTCTCTAGAGAGGGCTCTTGTCCTGTCAGAGCTGTTTT CTCC CTTCTCTTGTTTTTTCTTTTTCAAGACTGTTTCTCTGTGTTAGCCCTGGCTGTCCTGGAT CTCA CTCTGTAGATCAGGCTGACCTTGAGTTCAAAGCTCCATCTGCCTCTACTTCTCACATTAC TGTG ATTAAAGGCATATACTACCACTGCCTGGTGCCCTTTTGTATTTCTTATTAAAGTCCTAAT GTCT GATTATAAAAACAGTCTGTGTGGGCTGGAGTGATGGCTTACTCAGTAAAGCACTTGCCAT GGAA TCTGGGCAATCTGAGTTTCATTTTTAGCATCCTGTAAAAATCCCAATTTGATGGTGTACT TGTA AT G T C AG CAT G GAGAG G C AGAGAT AG G T AAG T T C C C C AAGAC T C T T T GAAC C GAC AG C T T G G C C TCACTGGCACATTCCAGGTCTCAGT GAG AG AC C C T G C C T C AAAAT AC AAAG AAAG AG C T G C T G A AGAGTGGGTCAGAGTTGACCTCTGATCTCCGGAAGTATATGATACACACCCGTGCATGCA CTCT T C C T T AC AAAAT AAAAAG C AAAAC AAAAC C C C AAC AG GTATATGGCCATTT T AGAAAAAT T AGA AGAT T TAGAAAGC TATACATAAAAAAAAAT GAC C T AAAGAAAAAT C T T TAC T GT T C TGGGCAC T ATCCCTATCAAACCACTGTGTTCTTTGGCCAAGCCTTGGGGTGGACACTGTTTTGAGGTG GGTC CTGTTATCTCCACTAGGTAGTGGAGTTTTGTGTCAGACTAACTGGGTCTTAAAGCTGTCT TTAA GGCCATCAGGAGCTACTGACTTGCCTGCCTCAGCAGAGCATATCCTGAAGGTCGGGGTTA AGTC TCCTTCCCGAGCGAGTTGCCTTCCAGTGGGCCCCTGGACTCCTAGGTCCTCAGCGCTCAT CAGC TGCCAAGGACTCTGAGGGAATGTCCTCTGACTGTGGCCCCGAAAGGTAGGGGAGGGGGAT GTGC TTAGGCTTAGGACAGGGTCCTGTTTCAGTCTGCCTTCACTGTTAGTAGCACTGTGCCACA TGGC ACAGACTGGGCGAGCTTTAAAGGAAGGAGGTTGATATTGGTTCCCACTTCTGGGGATCAT GGTT GAGCAGCCTTGTCTGATGATGGTTGTCTTGATGGTAGATCGTGAGGTAGTTGATGAAGGT ATGA CATGGTGAGAAACTCTGTGTGTGTGTGTTATTTTCTCTGTGTTCTACCTATACATCTATC TATG TATATATGTATCTATCTATC TAC C T G GAG G C T G GAGAGAT AG C T TAG T G G T T AAGAAC AT T T G T TGTTCTTG CAT AG T C C T G GAT T T AAAT T T T C AG C AC C C AC AT G G C AG C T C AC AAC AAC C C AT AA AT C C AG T T T C AGAG GAT C C AAC C T C T GAT AT AC CAT G T C AG C C AGAG C AGAC AC G G C T GAAG G T G G T T T GAT CCCCGTATG GAGAG G T GAC AAT T G G GAAGAGAGAAAGAT C AAC T T AAC CAT G C AAG GAAC AG GAAG T T AAAT AC T GAAC AG G GAAG G T AAAG G C AG GAAG T AGAT G T AGAG G G C AAAT C A AT GAAAC C C AAAC AT AC C C AAAT T AC G C T AAAC AC AC AC T GAC AT G C C AAT TAAAAG GAC AAAT T G G C T C C AC T G G C AAAAC C AAAAC AGAC AC T GAAGAT C C AAAC AG T C AC AT G C C AAC TAC C G C G GAG G GAGAC AGAC AC AGAGAAGAC C G T GAC AGAC AC T T G GAC AC T C T T GAGAG T G GAT G T G C AG GAAGAGAG C T C T G C C AG T G GAGAAGAAAG C AC T C AGAAGAAAG T GAC AG C AG C T G T AAAT T T G T ATTCTGCTAATGTTATGTTC C AAAG T T GAAAG C AAAAT T G T AC C AAT T CAT AAGAAC AAAC AG G CTGACTCTCAGTTGTGACTGAACGTCTCTCAGTAACTGACGGGGCGAGCAGGCCAAAGGA GAGT C G G C T C AGAAG G G T G C AT AGC C AC G C C AAAT C AAAT AAG C AAG TAC AAC C G G C AG GCTCTATTT CTAGCACAAAGGGGTCTGTGCCTCATTCTGTGCTTGGGTCAGAGCTTGGGTCTCTCATTT GGAT G T AAG T G G T G TAG T G GAGAAG C AG GAAAT AAT C C G GAG C G CAT AT T T T GAT T T T AAC AT AAG T G CTGATTTGGGAGGGAGTTTTGTCAAATTGTGTTTTTACAATGTTTTTTTTTTTTTAAATG ATGC T T T T T T G T AAAG T G T AC AAAT G T GAT AT AAGAT T G G T T C T G C T AC AT T C AG T T T C T AT AAAAG T GG T T C T AAAAT AT T G TAC T GT CAAT CAT C T CAT GAT TAT T C TAC T G T ACACAT TAC T GAC T T T G T AT G T AAT AAT T AAT AT T AGAAGAAAAT AT AAT T T AT T T GAAT AT AAAAAAAAAAAAAAAAAAA

[00386] SEQ ID NO: 46:

X1ASLPX2LQX3ESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVL RRGDYDAX4

THQVQWQAQEWAQARLDGHRSMNPCPLYDX ₅ QTGTLFLFFIAIPGQVTEQQQLQTRANVTRLCQ VT STDHGRTWSS PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPXeQRP

IPSAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQS TNDGLD

FQESQLVKKLVEPPPXvGCQGSVISFPSPRSGPGSPAQWLLYTHPTHXsXgQRADLG AYLNPRPP

APEAWSEPVLLAKGSX ₁₀ AYSDLQSMGTGPDGSPLFGCLYEANDYEEIX ₁₁ FX ₁₂ MFTLKQAFPAE

YLPQ

[00387] SEQ ID NO: 47:

X ₁ X ₂ SX ₃ X ₄ X ₅ LQX ₆ ESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASX ₇ X ₈ DEHAELIVX ₉ RRGD

YDAX10THQVQWX11AQEWAQAX12LDGHRSMNPCPLYDX13QTGTLFLFFIAIPX1 4X15VTEX16Q

QLQTRANVTRLX17X18VTSTDHGRTWSSPRDLTDAAIGPX19YREWSTFAVGPGHX 20LQLHDRX21

RSLWPAYAYRKLHPX ₂₂ QRPIPSAFX ₂₃ FLSHDHGRTWARGHFVAQDTX ₂₄ ECQVAEVETGEQRV

VTLNARSHLRARVQAQSX ₂₅ NX ₂₆ GLDFQX ₂₇ SQLVKKLVEPPPX ₂₈ GX ₂₉ QGSVISFPSPRSGPGSP

AQX ₃₀ LLYTHPTHX ₃₁ X ₃₂ QRADLGAYLNPRPPAPEAWSEPX ₃₃ LLAKGSX ₃₄ AYSDLQSMGTGPDGS

PLFGX ₃₅ LYEANDYEEIX ₃₆ FX ₃₇ MFTLKQAFPAEYLPQ

[00388] SEQ ID NO: 48:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDAGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSS PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPKQRP I P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00389] SEQ ID NO: 49:

DASLPYLQDESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSS PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPKQRP I P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIRFIMFTLKQAFPAEYLPQ

[00390] SEQ ID NO: 50:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD ANTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSS PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPKQRP I P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00391] SEQ ID NO: 51:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDAPTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSS PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPKQRP I P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ [00392] SEQ ID NO: 52:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDASTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00393] SEQ ID NO: 53 :

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDATTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00394] SEQ ID NO: 54:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDANTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00395] SEQ ID NO: 55:

ASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYDA PTHQ VQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLCQ VTS TDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQRP IPS AFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGLD FQE SQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPPA PEAW SEPVLLAKGSCAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00396] SEQ ID NO: 56:

MASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSCAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00397] SEQ ID NO: 57:

ASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYDA PTHQ VQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLCQ VTS TDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQRP IPS AFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGLD FQE SQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPPA PEAW

SEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYL PQ

[00398] SEQ ID NO: 58:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00399] SEQ ID NO: 59:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSCAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00400] SEQ ID NO: 60:

AASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00401] SEQ ID NO: 61 :

MASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00402] SEQ ID NO: 62:

AASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSCAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00403] SEQ ID NO: 63 :

EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYIMMWVRQAPGKGLEWVSS IYPSGGITFYADTV KGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARIKLGTVTTVDYWGQGTLVTVSSASTK GPSV FPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSW TVP

SSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPK PKDTLMI

SRTPEVTCVWDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQD WLNGK

EYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYP SDIAVEW

ESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQ KSLSLSP

GK

[00404] SEQ ID NO: 64:

QSALTQPASVSGSPGQSITISCTGTSSDVGGYNYVSWYQQHPGKAPKLMIYDVSNRPSGV SNRF

SGSKSGNTASLTISGLQAEDEADYYCSSYTSSSTRVFGTGTKVTVLGQPKANPTVTL FPPSSEE

LQANKATLVCLISDFYPGAVTVAWKADGSPVKAGVETTKPSKQSNNKYAASSYLSLT PEQWKSH

RSYSCQVTHEGSTVEKTVAPTECS

[00405] SEQ ID NO: 65:

QSALTQPASVSGSPGQSITISCTGTSSDVGGYNYVSWYQQHPGKAPKLMIYDVSNRPSGV SNRF

SGSKSGNTASLTISGLQAEDEADYYCSSYTSSSTRVFGTGTKVTVLGQPKANPTVTL FPPSSEE

LQANKATLVCLISDFYPGAVTVAWKADGSPVKAGVETTKPSKQSNNKYAASSYLSLT PEQWKSH

RSYSCQVTHEGSTVEKTVAPTECS

[00406] SEQ ID NO: 66:

EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYIMMWVRQAPGKGLEWVSS IYPSGGITFYADTV KGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARIKLGTVTTVDYWGQGTLVTVSSASTK GPSV FPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSW TVP SSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKD TLMI SRTPEVTCVWDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLN GK EYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLYCLVKGFYPSDI AVEW ESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSL SLSP GK

[00407] SEQ ID NO: 67:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDAGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ GGGG SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKF NWY VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKA KGQ PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFL TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00408] SEQ ID NO: 68:

DASLPYLQDESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA

WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIRFIMFTLKQAFPAEY LPQGGGG

SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPE VKFNWY

VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTI SKAKGQ

PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLD SDGSFFL

TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00409] SEQ ID NO: 69:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD ANTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ GGGG SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKF NWY VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKA KGQ PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFL TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00410] SEQ ID NO: 70:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ GGGG SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCWVDVSHEDPEVKF NWY VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKA KGQ PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFL TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00411] SEQ ID NO: 71 :

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD ASTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ GGGG SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKF NWY VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKA KGQ PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFL TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00412] SEQ ID NO: 72:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD ATTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA

WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEY LPQGGGG

SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPE VKFNWY

VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTI SKAKGQ

PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLD SDGSFFL

TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00413] SEQ ID NO: 73:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD ANTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ GGGG SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKF NWY VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKA KGQ PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFL TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00414] SEQ ID NO: 74:

X1ASLPX2LQX3ESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDAX4

THQVQWQAQEWAQARLDGHRSMNPCPLYDX ₅ QTGTLFLFFIAIPGQVTEQQQLQTRANVTRLCQ

VTSTDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKL HPXeQRP

IPSAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQS TNDGLD

FQESQLVKKLVEPPPXvGCQGSVISFPSPRSGPGSPAQWLLYTHPTHXsXgQRADLG AYLNPRPP

APEAWSEPVLLAKGSX ₁₀ AYSDLQSMGTGPDGSPLFGCLYEANDYEEIX ₁₁ FX ₁₂ MFTLKQAFPAE

YLPQGGGGSGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCWV DVSHED

PEVKFNWYVDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKAL PAPIEK

TISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNY KTTPPVL

DSDGSFFLTSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00415] SEQ ID NO: 75:

X ₁ X ₂ SX ₃ X ₄ X ₅ LQX ₆ ESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASX ₇ X ₈ DEHAELIVX ₉ RRGD

YDAX10THQVQWX11AQEWAQAX12LDGHRSMNPCPLYDX13QTGTLFLFFIAIPX1 4X15VTEX16Q

QLQTRANVTRLX17X18VTSTDHGRTWSSPRDLTDAAIGPX19YREWSTFAVGPGHX 20LQLHDRX21

RSLWPAYAYRKLHPX ₂₂ QRPIPSAFX ₂₃ FLSHDHGRTWARGHFVAQDTX ₂₄ ECQVAEVETGEQRV

VTLNARSHLRARVQAQSX ₂₅ NX ₂₆ GLDFQX ₂₇ SQLVKKLVEPPPX ₂₈ GX ₂₉ QGSVISFPSPRSGPGSP

AQX ₃₀ LLYTHPTHX ₃₁ X ₃₂ QRADLGAYLNPRPPAPEAWSEPX ₃₃ LLAKGSX ₃₄ AYSDLQSMGTGPDGS

PLFGX ₃₅ LYEANDYEEIX ₃₆ FX ₃₇ MFTLKQAFPAEYLPQGGGGSGGGGSDKTHTCPPCPAPELLGG

PSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQ YNSTYR

WSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMT KNQVSL

TCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLTSKLTVDKSRWQQGNV FSCSVMH

EALHNHYTQKSLSLSPGK

[00416] SEQ ID NO: 76:

CAATCTGCTCTTACACAGCCTGCCAGCGTGTCCGGATCTCCTGGCCAGAGCATCACCATC AGCT

GTACCGGCACCAGCTCTGATGTCGGCGGCTACAATTACGTGTCCTGGTATCAGCAGC ACCCCGG CAAGGCCCCTAAGCTGATGATCTACGACGTGTCCAACAGACCCAGCGGCGTGTCCAATAG ATTC TCCGGCAGCAAGAGCGGCAACACCGCCAGCCTGACAATTAGCGGACTGCAGGCCGAGGAC GAGG CCGATTACTACTGTAGCAGCTACACCAGCTCCAGCACCAGAGTGTTTGGCACCGGCACAA AAGT GACCGTGCTGGGCCAGCCTAAGGCCAATCCTACCGTGACACTGTTCCCTCCAAGCAGCGA GGAA CTGCAGGCTAACAAGGCCACACTCGTGTGCCTGATCAGCGACTTTTATCCTGGCGCCGTG ACCG TGGCCTGGAAGGCTGATGGATCTCCAGTGAAAGCCGGCGTGGAAACCACCAAGCCTAGCA AGCA GAGCAACAACAAATACGCCGCCAGCAGCTACCTGAGCCTGACACCTGAGCAGTGGAAGTC CCAC AGATCCTACAGCTGCCAAGTGACCCACGAGGGCAGCACCGTGGAAAAAACAGTGGCCCCT ACCG AGTGCTCT

[00417] SEQ ID NO: 77:

GAGGTGCAGCTGCTGGAATCTGGCGGAGGACTTGTTCAGCCTGGCGGCTCTCTGAGACTG TCTT GTGCCGCCAGCGGCTTCACCTTCAGCAGCTATATCATGATGTGGGTCCGACAGGCCCCTG GCAA AGGCCTTGAATGGGTGTCCAGCATCTATCCCAGCGGCGGCATCACCTTTTACGCCGACAC AGTG AAGGGCAGATTCACCATCAGCCGGGACAACAGCAAGAACACCCTGTACCTGCAGATGAAC AGCC TGAGAGCCGAGGACACCGCCGTGTACTACTGCGCCAGAATCAAGCTGGGCACCGTGACCA CCGT GGATTATTGGGGACAGGGCACCCTGGTCACCGTGTCATCTGCTAGCACCAAGGGCCCATC CGTC TTCCCCCTGGCACCCTCCTCCAAGAGCACCTCTGGGGGCACAGCGGCCCTGGGCTGCCTG GTCA AGGACTACTTCCCCGAACCGGTGACGGTGTCCTGGAACTCAGGCGCTCTGACCAGCGGCG TGCA CACCTTCCCGGCTGTCCTACAGTCCTCAGGACTCTACTCCCTCAGCAGCGTGGTGACCGT GCCC TCCAGCAGCTTGGGCACCCAGACCTACATCTGCAACGTGAATCACAAGCCCAGCAACACC AAGG TGGACAAGAAAGTTGAGCCCAAATCTTGTGACAAAACTCACACATGCCCACCGTGCCCAG CACC TGAACTCCTGGGGGGACCGTCAGTCTTCCTCTTCCCCCCAAAACCCAAGGACACCCTCAT GATC TCCCGGACCCCTGAGGTCACATGCGTGGTGGTGGACGTGAGCCACGAAGACCCTGAGGTC AAGT TCAACTGGTACGTGGACGGCGTGGAGGTGCATAATGCCAAGACAAAGCCGCGGGAGGAGC AGTA CAACAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCACCAGGACTGGCTGAATGG CAAG GAGTACAAGTGCAAGGTCTCCAACAAAGCCCTCCCAGCCCCCATCGAGAAAACCATCTCC AAAG CCAAAGGGCAGCCCCGAGAACCACAGGTCTACACCCTGCCCCCATCCCGGGAGGAGATGA CCAA GAACCAGGTCAGCCTGTACTGCCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGA GTGG GAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCACGCCTCCCGTGCTGGACTCCGAC GGCT CCTTCTTCCTCTATAGCAAGCTCACCGTGGACAAGAGCAGGTGGCAGCAGGGGAACGTCT TCTC ATGCTCCGTGATGCATGAGGCTCTGCACAACCACTACACGCAGAAGAGCCTCTCCCTGTC TCCG GGTAAA

[00418] SEQ ID NO: 78:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PI P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ GGGG SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLT SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00419] SEQ ID NO: 79:

GATGCATCTCTGCCTTACCTGCAGAAAGAAAGCGTGTTCCAGTCTGGCGCCCACGCCTAC AGAA

TTCCCGCTCTGCTGTATCTGCCAGGCCAGCAGTCTCTGCTGGCTTTCGCTGAACAGC GGGCCAG C AAGAAG GAT GAG C AC G C C GAAC T GAT CGTGCTGCG GAGAG G C GAT T AC GAC G C C G G C AC AC AT CAGGTGCAGTGGCAGGCTCAAGAGGTGGTGGCTCAGGCTAGACTGGACGGCCACAGATCT ATGA ACCCCTGTCCTCTGTACGATGAACAGACCGGCACACTGT T TCTGT TCT T TATCGCTATCCCCGG C C AAG T GAC C GAG C AG C AG C AG C T G C AG AC AAG AG C C AAC G T GAC C AG AC T G T G T C AAG T GAC C TCCACCGACCACGGCAGAACCTGGTCTAGCCCTAGAGATCTGACCGACGCCGCCATCGGA CCTG CCTATAGAGAGTGGTCCACCT TCGCCGT TGGACCTGGACACTGTCTCCAGCTGCACGACAGGGC TAGATCTCTGGTGGTGCCTGCCTACGCCTATAGAAAGCTGCACCCCAAACAGCGGCCTAT TCCT AGCGCCT TCTGCT T TCTGAGCCACGATCACGGCAGGACATGGGCCAGAGGACAT T TCGTGGCCC AGGACACACTGGAATGCCAGGTGGCCGAAGTGGAAACCGGCGAGCAGAGAGTCGTGACCC TGAA C G C C AGAT C T C AC C T GAGAGC C AGAG T G C AG G C C C AGAG C AC AAAC GAC G G C C T G GAT T T C C AA GAGAGCCAGCTGGTCAAGAAACTGGTGGAACCTCCTCCACAGGGCTGTCAGGGAAGCGTG ATCA GCT T TCCATCTCCTAGAAGCGGCCCTGGCTCTCCTGCTCAGTGGCTGCTGTATACACACCCCAC ACACAGCTGGCAGAGAGCCGATCTGGGCGCCTACCTGAATCCTAGACCTCCTGCTCCTGA GGCT TGGAGCGAACCTGT TCTGCTGGCCAAGGGCAGCGCTGCCTACAGCGATCTGCAGTCTATGGGCA CAGGCCCTGATGGCAGCCCTCTGT T TGGCTGTCTGTACGAGGCCAACGACTACGAAGAGATCGT GT TCCTGATGT TCACCCTGAAGCAGGCCT T TCCAGCCGAGTACCTGCCTCAAGGCGGAGGCGGA TCCGACAAAACTCACACATGCCCACCGTGCCCAGCACCTGAACTCCTGGGGGGACCGTCA GTCT TCCTCT TCCCCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCCTGAGGTCACATGCGT GGTGGTGGACGTGAGCCACGAAGACCCTGAGGTCAAGT TCAACTGGTACGTGGACGGCGTGGAG GTGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTACAACAGCACGTACCGTGTGGTC AGCG TCCTCACCGTCCTGCACCAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCTCCA ACAA AGCCCTCCCAGCCCCCATCGAGAAAACCATCTCCAAAGCCAAAGGGCAGCCCCGAGAACC ACAG GTCTACACCCTGCCCCCATCCCGGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTGC CTGG TCAAAGGCT TCTATCCCAGCGACATCGCCGTGGAGTGGGAGAGCAATGGGCAGCCGGAGAACAA CTACAAGACCACGCCTCCCGTGCTGGACTCCGACGGCTCCT TCT TCCTCACTAGCAAGCTCACC GTGGACAAGAGCAGGTGGCAGCAGGGGAACGTCT TCTCATGCTCCGTGATGCATGAGGCTCTGC ACAACCACTACACGCAGAAGAGCCTCTCCCTGTCTCCGGGTAAA

[00420] SEQ ID NO: 80:

GATGCATCTCTGCCT TACCTGCAGAAAGAAAGCGTGT TCCAGTCTGGCGCCCACGCCTACAGAA T TCCCGCTCTGCTGTATCTGCCAGGCCAGCAGTCTCTGCTGGCT T TCGCTGAACAGCGGGCCAG C AAGAAG GAT GAG C AC G C C GAAC T GAT CGTGCTGCG GAGAG G C GAT T AC GAC G C C G G C AC AC AT CAGGTGCAGTGGCAGGCTCAAGAGGTGGTGGCTCAGGCTAGACTGGACGGCCACAGATCT ATGA ACCCCTGTCCTCTGTACGATGAACAGACCGGCACACTGT T TCTGT TCT T TATCGCTATCCCCGG C C AAG T GAC C GAG C AG C AG C AG C T G C AG AC AAG AG C C AAC G T GAC C AG AC T G T G T C AAG T GAC C TCCACCGACCACGGCAGAACCTGGTCTAGCCCTAGAGATCTGACCGACGCCGCCATCGGA CCTG CCTATAGAGAGTGGTCCACCTTCGCCGT TGGACCTGGACACTGTCTCCAGCTGCACGACAGGGC TAGATCTCTGGTGGTGCCTGCCTACGCCTATAGAAAGCTGCACCCCAAACAGCGGCCTAT TCCT AGCGCCT TCTGCT T TCTGAGCCACGATCACGGCAGGACATGGGCCAGAGGACAT T TCGTGGCCC AGGACACACTGGAATGCCAGGTGGCCGAAGTGGAAACCGGCGAGCAGAGAGTCGTGACCC TGAA C G C C AG AT C T C AC C T GAGAG C C AG AG TGCAGGCC C AG AG C AC AAAC GAC G G C C T G GAT T T C C AA GAGAGCCAGCTGGTCAAGAAACTGGTGGAACCTCCTCCACAGGGCTGTCAGGGAAGCGTG ATCA GCT T TCCATCTCCTAGAAGCGGCCCTGGCTCTCCTGCTCAGTGGCTGCTGTATACACACCCCAC ACACAGCTGGCAGAGAGCCGATCTGGGCGCCTACCTGAATCCTAGACCTCCTGCTCCTGA GGCT TGGAGCGAACCTGT TCTGCTGGCCAAGGGCAGCGCTGCCTACAGCGATCTGCAGTCTATGGGCA CAGGCCCTGATGGCAGCCCTCTGT T TGGCTGTCTGTACGAGGCCAACGACTACGAAGAGATCGT GT TCCTGATGT TCACCCTGAAGCAGGCCT T TCCAGCCGAGTACCTGCCTCAA [00421] SEQ ID NO: 81 :

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDAGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLT SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00422] SEQ ID NO: 82:

DASLPYLQDESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIRFIMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLT SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00423] SEQ ID NO: 83 :

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD ANTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLT SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00424] SEQ ID NO: 84:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD APTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLT SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK [00425] SEQ ID NO: 85:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD ASTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSS PRDLTDAAI GPAYREWST FAVGPGHCLQLHDRARS LWPAYAYRKLHPKQRP I P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLT SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00426] SEQ ID NO: 86:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD ATTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSS PRDLTDAAI GPAYREWST FAVGPGHCLQLHDRARS LWPAYAYRKLHPKQRP I P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLT SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00427] SEQ ID NO: 87:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD ANTH QVQWQAQEWAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSS PRDLTDAAI GPAYREWST FAVGPGHCLQLHDRARS LWPAYAYRKLHPKQRP I P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPAGCQGSVISFPSPRSGPGSPAQWLLYTHPTHRKQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLT SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00428] SEQ ID NO: 88:

X1ASLPX2LQX3ESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVL RRGDYDAX4

THQVQWQAQEWAQARLDGHRSMNPCPLYDX ₅ QTGTLFLFFIAIPGQVTEQQQLQTRANVTRLCQ

VT STDHGRTWSS PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPXeQRP

IPSAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQS TNDGLD

FQESQLVKKLVEPPPXvGCQGSVISFPSPRSGPGSPAQWLLYTHPTHXsXgQRADLG AYLNPRPP

APEAWSEPVLLAKGSX ₁₀ AYSDLQSMGTGPDGSPLFGCLYEANDYEEIX ₁₁ FX ₁₂ MFTLKQAFPAE

YLPQX ₁₃ DKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKF NWY

VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTI SKAKGQ

PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLD SDGSFFL

TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK [00429] SEQ ID NO: 89:

X ₁ X ₂ SX ₃ X ₄ X ₅ LQX ₆ ESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASX ₇ X ₈ DEHAELIVX ₉ RRGD

YDAX10THQVQWX11AQEWAQAX12LDGHRSMNPCPLYDX13QTGTLFLFFIAIPX1 4X15VTEX16Q

QLQTRANVTRLX17X18VTSTDHGRTWSSPRDLTDAAIGPX19YREWSTFAVGPGHX 20LQLHDRX21

RSLWPAYAYRKLHPX ₂₂ QRPIPSAFX ₂₃ FLSHDHGRTWARGHFVAQDTX ₂₄ ECQVAEVETGEQRV

VTLNARSHLRARVQAQSX ₂₅ NX ₂₆ GLDFQX ₂₇ SQLVKKLVEPPPX ₂₈ GX ₂₉ QGSVISFPSPRSGPGSP

AQX ₃₀ LLYTHPTHX ₃₁ X ₃₂ QRADLGAYLNPRPPAPEAWSEPX ₃₃ LLAKGSX ₃₄ AYSDLQSMGTGPDGS

PLFGX ₃₅ LYEANDYEEIX ₃₆ FX ₃₇ MFTLKQAFPAEYLPQX ₃₈ DKTHTCPPCPAPELLGGPSVFLFPP

KPKDTLMISRTPEVTCWVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRWS VLTVL

HQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLT CLVKGFY

PSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLTSKLTVDKSRWQQGNVFSCSVMHE ALHNHYT

QKSLSLSPGK

[00430] SEQ ID NO: 90:

GGGGSGGGGS

[00431] SEQ ID NO: 91 :

EPKSS

[00432] SEQ ID NO: 92:

EPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCWVDVSHEDPEVKFN WYV

DGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTIS KAKGQP

REPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDS DGSFFLT

SKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00433] SEQ ID NO: 93:

DKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVDG VEV

HNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQ PREPQV

YTLPPSREEMTKNQVSLYCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFF LYSKLTV

DKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00434] SEQ ID NO: 94:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHARQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00435] SEQ ID NO: 95:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ

ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHARQRADLGAYLNP RPPAPEA

WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEY LPQGGGG

SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPE VKFNWY

VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTI SKAKGQ

PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLD SDGSFFL

TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00436] SEQ ID NO: 96:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHARQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLT SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00437] SEQ ID NO: 97:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDAGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC YVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPTGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00438] SEQ ID NO: 98:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDAGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC YVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPTGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ GGGG SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKF NWY VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKA KGQ PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFL TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00439] SEQ ID NO: 99:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC YVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPTGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ

VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSF FLTSKLT

VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00440] SEQ ID NO: 100:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC YVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PI P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRFRVQAQSTNDGL DFQ ESQLVKKLVEPPPTGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00441] SEQ ID NO: 101 :

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC YVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PI P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRFRVQAQSTNDGL DFQ ESQLVKKLVEPPPTGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ GGGG SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKF NWY VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKA KGQ PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFL TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00442] SEQ ID NO 102:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC YVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PI P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRFRVQAQSTNDGL DFQ ESQLVKKLVEPPPTGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLT SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00443] SEQ ID NO 103:

GATGCATCTCTGCCTTACCTGCAGAAAGAAAGCGTGTTCCAGTCTGGCGCCCACGCCTAC AGAA TTCCCGCTCTGCTGTATCTGCCAGGCCAGCAGTCTCTGCTGGCTTTCGCTGAACAGCGGG CCAG CAAGAAGGATGAGCACGCCGAACTGATCGTGCTGCGGAGAGGCGATTACGACGCCGGCAC ACAT CAGGTGCAGTGGCAGGCTCAAGAGGTGGTGGCTCAGGCTAGACTGGACGGCCACAGATCT ATGA ACCCCTGTCCTCTGTACGATGAACAGACCGGCACACTGTTTCTGTTCTTTATCGCTATCC CCGG CCAAGTGACCGAGCAGCAGCAGCTGCAGACAAGAGCCAACGTGACCAGACTGTGTCAAGT GACC TCCACCGACCACGGCAGAACCTGGTCTAGCCCTAGAGATCTGACCGACGCCGCCATCGGA CCTG CCTATAGAGAGTGGTCCACCTTCGCCGTTGGACCTGGACACTGTCTCCAGCTGCACGACA GGGC TAGATCTCTGGTGGTGCCTGCCTACGCCTATAGAAAGCTGCACCCCAAACAGCGGCCTAT TCCT AGCGCCTTCTGCTTTCTGAGCCACGATCACGGCAGGACATGGGCCAGAGGACATTTCGTG GCCC AGGACACACTGGAATGCCAGGTGGCCGAAGTGGAAACCGGCGAGCAGAGAGTCGTGACCC TGAA CGCCAGATCTCACCTGAGAGCCAGAGTGCAGGCCCAGAGCACAAACGACGGCCTGGATTT CCAA GAGAGCCAGCTGGTCAAGAAACTGGTGGAACCTCCTCCACAGGGCTGTCAGGGAAGCGTG ATCA GCTTTCCATCTCCTAGAAGCGGCCCTGGCTCTCCTGCTCAGTGGCTGCTGTATACACACC CCAC ACACAGCTGGCAGAGAGCCGATCTGGGCGCCTACCTGAATCCTAGACCTCCTGCTCCTGA GGCT TGGAGCGAACCTGTTCTGCTGGCCAAGGGCAGCGCTGCCTACAGCGATCTGCAGTCTATG GGCA CAGGCCCTGATGGCAGCCCTCTGTTTGGCTGTCTGTACGAGGCCAACGACTACGAAGAGA TCGT GTTCCTGATGTTCACCCTGAAGCAGGCCTTTCCAGCCGAGTACCTGCCTCAAGGCGGAGG CGGA TCCGACAAAACTCACACATGCCCACCGTGCCCAGCACCTGAACTCCTGGGGGGACCGTCA GTCT TCCTCTTCCCCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCCTGAGGTCACAT GCGT GGTGGTGGACGTGAGCCACGAAGACCCTGAGGTCAAGTTCAACTGGTACGTGGACGGCGT GGAG GTGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTACAACAGCACGTACCGTGTGGTC AGCG TCCTCACCGTCCTGCACCAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCTCCA ACAA AGCCCTCCCAGCCCCCATCGAGAAAACCATCTCCAAAGCCAAAGGGCAGCCCCGAGAACC ACAG GTCTACACCCTGCCCCCATCCCGGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTGC CTGG TCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAGTGGGAGAGCAATGGGCAGCCGGAGA ACAA CTACAAGACCACGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCACTAGCAAGCT CACC GTGGACAAGAGCAGGTGGCAGCAGGGGAACGTCTTCTCATGCTCCGTGATGCATGAGGCT CTGC ACAACCACTACACGCAGAAGAGCCTCTCCCTGTCTCCGGGTAAA

[00444] SEQ ID NO: 104:

EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYIMMWVRQAPGKGLEWVSS IYPSGGITFYADTV KGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARIKLGTVTTVDYWGQGTLVTVSSASTK GPSV FPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSW TVP SSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKD TLMI SRTPEVTCVWDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYGSTYRWSVLTVLHQDWLN GK EYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLYCLVKGFYPSDI AVEW ESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSL SLSP GK

[00445] SEQ ID NO: 105:

GAGGTGCAGCTGCTGGAATCTGGCGGAGGACTTGTTCAGCCTGGCGGCTCTCTGAGACTG TCTT GTGCCGCCAGCGGCTTCACCTTCAGCAGCTATATCATGATGTGGGTCCGACAGGCCCCTG GCAA AGGCCTTGAATGGGTGTCCAGCATCTATCCCAGCGGCGGCATCACCTTTTACGCCGACAC AGTG AAGGGCAGATTCACCATCAGCCGGGACAACAGCAAGAACACCCTGTACCTGCAGATGAAC AGCC TGAGAGCCGAGGACACCGCCGTGTACTACTGCGCCAGAATCAAGCTGGGCACCGTGACCA CCGT GGATTATTGGGGACAGGGCACCCTGGTCACCGTGTCATCTGCTAGCACCAAGGGCCCATC CGTC TTCCCCCTGGCACCCTCCTCCAAGAGCACCTCTGGGGGCACAGCGGCCCTGGGCTGCCTG GTCA AGGACTACTTCCCCGAACCGGTGACGGTGTCCTGGAACTCAGGCGCTCTGACCAGCGGCG TGCA CACCTTCCCGGCTGTCCTACAGTCCTCAGGACTCTACTCCCTCAGCAGCGTGGTGACCGT GCCC TCCAGCAGCTTGGGCACCCAGACCTACATCTGCAACGTGAATCACAAGCCCAGCAACACC AAGG TGGACAAGAAAGTTGAGCCCAAATCTTGTGACAAAACTCACACATGCCCACCGTGCCCAG CACC TGAACTCCTGGGGGGACCGTCAGTCTTCCTCTTCCCCCCAAAACCCAAGGACACCCTCAT GATC TCCCGGACCCCTGAGGTCACATGCGTGGTGGTGGACGTGAGCCACGAAGACCCTGAGGTC AAGT TCAACTGGTACGTGGACGGCGTGGAGGTGCATAATGCCAAGACAAAGCCGCGGGAGGAGC AGTA CGGTAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCACCAGGACTGGCTGAATGG CAAG GAGTACAAGTGCAAGGTCTCCAACAAAGCCCTCCCAGCCCCCATCGAGAAAACCATCTCC AAAG CCAAAGGGCAGCCCCGAGAACCACAGGTCTACACCCTGCCCCCATCCCGGGAGGAGATGA CCAA GAACCAGGTCAGCCTGTACTGCCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGA GTGG GAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCACGCCTCCCGTGCTGGACTCCGAC GGCT

CCTTCTTCCTCTATAGCAAGCTCACCGTGGACAAGAGCAGGTGGCAGCAGGGGAACG TCTTCTC

ATGCTCCGTGATGCATGAGGCTCTGCACAACCACTACACGCAGAAGAGCCTCTCCCT GTCTCCG

GGTAAA

[00446] SEQ ID NO: 106:

TVEKSWFKAEGEHFTDQKGNTIVGSGSGGTTKYFRIPAMCTTSKGTIWFADARHNTASDQ SF IDTAAARSTDGGKTWNKKIAIYNDRVNSKLSRVMDPTCIVANIQGRETILVMVGKWNNND KTWG AYRDKAPDTDWDLVLYKSTDDGVTFSKVETNIHDIVTKNGTISAMLGGVGSGLQLNDGKL VFPV QMVRTKNITTVLNTSFIYSTDGITWSLPSGYCEGFGSENNI IEFNASLVNNIRNSGLRRSFETK DFGKTWTEFPPMDKKVDNRNHGVQGST I T I PSGNKLVAAHSSAQNKNNDYTRSDI SLYAHNLYS GEVKLIDDFYPKVGNASGAGYSCLSYRKNVDKETLYVVYEANGS IEFQDLSRHLPVIKSYNGGG GSGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVK FNW YVDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISK AKG QPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSD GSFF LTSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGKSGGGGSHHHHHHHH

[00447] SEQ ID NO: 107:

ACAGTGGAAAAGTCCGTGGTGTTCAAGGCCGAGGGCGAGCACTTCACCGACCAGAAAGGC AATA CCATCGTCGGCTCTGGCAGCGGCGGCACCACCAAGTACTTTAGAATCCCCGCCATGTGCA CCAC CAGCAAGGGCACCATTGTGGTGTTCGCCGACGCCAGACACAACACCGCCAGCGATCAGAG CTTC ATCGATACCGCTGCCGCCAGAAGTACAGACGGCGGCAAGACCTGGAACAAGAAGATCGCC ATCT ACAACGACCGCGTGAACAGCAAGCTGAGCAGAGTGATGGACCCTACCTGCATCGTGGCCA ACAT CCAGGGCAGAGAAACCATCCTGGTCATGGTCGGAAAGTGGAACAACAACGATAAGACCTG GGGC GCCTACAGAGACAAGGCCCCTGATACCGATTGGGACCTCGTGCTGTATAAGAGCACCGAC GACG GCGTGACCTTCAGCAAGGTGGAAACAAACATCCACGACATCGTGACCAAGAACGGCACCA TCTC TGCCATGCTCGGCGGCGTTGGATCTGGCCTGCAACTGAATGATGGCAAGCTGGTGTTCCC CGTG CAGATGGTCCGAACAAAGAACATCACCACCGTGCTGAATACCAGCTTCATCTACTCCACC GACG GCATCACATGGTCCCTGCCTAGCGGCTACTGTGAAGGCTTTGGCAGCGAGAACAACATCA TCGA GTTCAACGCCAGCCTGGTCAACAACATCCGGAACAGCGGCCTGCGGAGAAGCTTCGAGAC AAAG GACTTCGGAAAGACGTGGACCGAGTTTCCTCCAATGGACAAGAAGGTGGACAACCGGAAC CACG GCGTGCAGGGCAGCACAATCACAATCCCTAGCGGCAACAAACTGGTGGCCGCTCACTCTA GCGC CCAGAACAAGAACAACGATTACACCAGAAGCGACATCAGCCTGTACGCCCACAACCTGTA CTCC GGCGAAGTGAAGCTGATCGACGACTTCTACCCCAAAGTGGGCAATGCCAGCGGAGCCGGC TACA GCTGTCTGAGCTACCGGAAAAATGTGGACAAAGAAACCCTGTACGTGGTGTACGAGGCCA ACGG CAGCATCGAGTTTCAGGACCTGAGCAGACATCTGCCCGTGATCAAGAGCTACAATGGCGG AGGT GGAAGTGGCGGAGGCGGATCCGACAAAACTCACACATGCCCACCGTGCCCAGCACCTGAA CTCC TGGGGGGACCGTCAGTCTTCCTCTTCCCCCCAAAACCCAAGGACACCCTCATGATCTCCC GGAC CCCTGAGGTCACATGCGTGGTGGTGGACGTGAGCCACGAAGACCCTGAGGTCAAGTTCAA CTGG TACGTGGACGGCGTGGAGGTGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTACAAC AGCA CGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCACCAGGACTGGCTGAATGGCAAGGAGT ACAA GTGCAAGGTCTCCAACAAAGCCCTCCCAGCCCCCATCGAGAAAACCATCTCCAAAGCCAA AGGG CAGCCCCGAGAACCACAGGTCTACACCCTGCCCCCATCCCGGGAGGAGATGACCAAGAAC CAGG TCAGCCTGACCTGCCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAGTGGGAGA GCAA TGGGCAGCCGGAGAACAACTACAAGACCACGCCTCCCGTGCTGGACTCCGACGGCTCCTT CTTC CTCACTAGCAAGCTCACCGTGGACAAGAGCAGGTGGCAGCAGGGGAACGTCTTCTCATGC TCCG TGATGCATGAGGCTCTGCACAACCACTACACGCAGAAGAGCCTCTCCCTGTCTCCGGGTA AAAG CGGCGGAGGCGGATCTCATCATCACCATCATCACCATCAC [00448] SEQ ID NO: 108:

TVEKSWFKAEGEHFTDQKGNTIVGSGSGGTTKYFRIPAMCTTSKGTIWFADARHNTASDQ SF IDTAAARSTDGGKTWNKKIAIYNDRVNSKLSRVMDPTCIVANIQGRETILVMVGKWNNND KTWG AYRDKAPDTDWDLVLYKSTDDGVTFSKVETNIHDIVTKNGTISAMLGGVGSGLQLNDGKL VFPV QMVRTKNITTVLNTSFIYSTDGITWSLPSGYCEGFGSENNI IEFNASLVNNIRNSGLRRSFETK DFGKTWTEFPPMDKKVDNRNHGVQGST I T I PSGNKLVAAHSSAQNKNNDYTRSDI SLYAHNLYS GEVKLIDDFYPKVGNASGAGYSCLSYRKNVDKETLYWYEANGSIEFQDLSRHLPVIKSYN GGG GSGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVK FNW YVDGVEVHNAKTKPREEQYGSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISK AKG QPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSD GSFF LTSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGKSGGGGSHHHHHHHH

[00449] SEQ ID NO 109:

ACAGTGGAAAAGTCCGTGGTGTTCAAGGCCGAGGGCGAGCACTTCACCGACCAGAAAGGC AATA CCATCGTCGGCTCTGGCAGCGGCGGCACCACCAAGTACTTTAGAATCCCCGCCATGTGCA CCAC CAGCAAGGGCACCATTGTGGTGTTCGCCGACGCCAGACACAACACCGCCAGCGATCAGAG CTTC ATCGATACCGCTGCCGCCAGAAGTACAGACGGCGGCAAGACCTGGAACAAGAAGATCGCC ATCT ACAACGACCGCGTGAACAGCAAGCTGAGCAGAGTGATGGACCCTACCTGCATCGTGGCCA ACAT CCAGGGCAGAGAAACCATCCTGGTCATGGTCGGAAAGTGGAACAACAACGATAAGACCTG GGGC GCCTACAGAGACAAGGCCCCTGATACCGATTGGGACCTCGTGCTGTATAAGAGCACCGAC GACG GCGTGACCTTCAGCAAGGTGGAAACAAACATCCACGACATCGTGACCAAGAACGGCACCA TCTC TGCCATGCTCGGCGGCGTTGGATCTGGCCTGCAACTGAATGATGGCAAGCTGGTGTTCCC CGTG CAGATGGTCCGAACAAAGAACATCACCACCGTGCTGAATACCAGCTTCATCTACTCCACC GACG GCATCACATGGTCCCTGCCTAGCGGCTACTGTGAAGGCTTTGGCAGCGAGAACAACATCA TCGA GTTCAACGCCAGCCTGGTCAACAACATCCGGAACAGCGGCCTGCGGAGAAGCTTCGAGAC AAAG GACTTCGGAAAGACGTGGACCGAGTTTCCTCCAATGGACAAGAAGGTGGACAACCGGAAC CACG GCGTGCAGGGCAGCACAATCACAATCCCTAGCGGCAACAAACTGGTGGCCGCTCACTCTA GCGC CCAGAACAAGAACAACGATTACACCAGAAGCGACATCAGCCTGTACGCCCACAACCTGTA CTCC GGCGAAGTGAAGCTGATCGACGACTTCTACCCCAAAGTGGGCAATGCCAGCGGAGCCGGC TACA GCTGTCTGAGCTACCGGAAAAATGTGGACAAAGAAACCCTGTACGTGGTGTACGAGGCCA ACGG CAGCATCGAGTTTCAGGACCTGAGCAGACATCTGCCCGTGATCAAGAGCTACAATGGCGG AGGT GGAAGTGGCGGAGGCGGATCCGACAAAACTCACACATGCCCACCGTGCCCAGCACCTGAA CTCC TGGGGGGACCGTCAGTCTTCCTCTTCCCCCCAAAACCCAAGGACACCCTCATGATCTCCC GGAC CCCTGAGGTCACATGCGTGGTGGTGGACGTGAGCCACGAAGACCCTGAGGTCAAGTTCAA CTGG TACGTGGACGGCGTGGAGGTGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTACGGT AGCA CGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCACCAGGACTGGCTGAATGGCAAGGAGT ACAA GTGCAAGGTCTCCAACAAAGCCCTCCCAGCCCCCATCGAGAAAACCATCTCCAAAGCCAA AGGG CAGCCCCGAGAACCACAGGTCTACACCCTGCCCCCATCCCGGGAGGAGATGACCAAGAAC CAGG TCAGCCTGACCTGCCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAGTGGGAGA GCAA TGGGCAGCCGGAGAACAACTACAAGACCACGCCTCCCGTGCTGGACTCCGACGGCTCCTT CTTC CTCACTAGCAAGCTCACCGTGGACAAGAGCAGGTGGCAGCAGGGGAACGTCTTCTCATGC TCCG TGATGCATGAGGCTCTGCACAACCACTACACGCAGAAGAGCCTCTCCCTGTCTCCGGGTA AAAG CGGCGGAGGCGGATCTCATCATCACCATCATCACCATCAC

[00450] SEQ ID NO: 110:

EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYIMMWVRQAPGKGLEWVSS IYPSGGITFYADTV KGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARIKLGTVTTVDYWGQGTLVTVSSASTK GPSV FPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSW TVP SSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKD TLMI SRTPEVTCWVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLN GK EYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLYCLVKGFYPSDI AVEW ESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSL SLSP GKGGGGSGGGGSGGGGSQSALTQPASVSGSPGQSITISCTGTSSDVGGYNYVSWYQQHPG KAPK LMIYDVSNRPSGVSNRFSGSKSGNTASLTISGLQAEDEADYYCSSYTSSSTRVFGTGTKV TVLG QPKAGGGGSGGGGSGGGGSEVQLLESGGGLVQPGGSLRLSCAASGFTFSSYIMMWVRQAP GKGL EWVSS IYPSGGITFYADTVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARIKLGTVTTVDY WGQGTLVTVSS

[00451] SEQ ID NO: 111 :

GAGGTGCAGCTGCTGGAATCTGGCGGAGGACTTGTTCAGCCTGGCGGCTCTCTGAGA CTGTCTT GTGCCGCCAGCGGCTTCACCTTCAGCAGCTATATCATGATGTGGGTCCGACAGGCCCCTG GCAA AGGCCTTGAATGGGTGTCCAGCATCTATCCCAGCGGCGGCATCACCTTTTACGCCGACAC AGTG AAGGGCAGATTCACCATCAGCCGGGACAACAGCAAGAACACCCTGTACCTGCAGATGAAC AGCC TGAGAGCCGAGGACACCGCCGTGTACTACTGCGCCAGAATCAAGCTGGGCACCGTGACCA CCGT GGATTATTGGGGACAGGGCACCCTGGTCACCGTGTCATCTGCTAGCACCAAGGGCCCATC CGTC TTCCCCCTGGCACCCTCCTCCAAGAGCACCTCTGGGGGCACAGCGGCCCTGGGCTGCCTG GTCA AGGACTACTTCCCCGAACCGGTGACGGTGTCCTGGAACTCAGGCGCTCTGACCAGCGGCG TGCA CACCTTCCCGGCTGTCCTACAGTCCTCAGGACTCTACTCCCTCAGCAGCGTGGTGACCGT GCCC TCCAGCAGCTTGGGCACCCAGACCTACATCTGCAACGTGAATCACAAGCCCAGCAACACC AAGG TGGACAAGAAAGTTGAGCCCAAATCTTGTGACAAAACTCACACATGCCCACCGTGCCCAG CACC TGAACTCCTGGGGGGACCGTCAGTCTTCCTCTTCCCCCCAAAACCCAAGGACACCCTCAT GATC TCCCGGACCCCTGAGGTCACATGCGTGGTGGTGGACGTGAGCCACGAAGACCCTGAGGTC AAGT TCAACTGGTACGTGGACGGCGTGGAGGTGCATAATGCCAAGACAAAGCCGCGGGAGGAGC AGTA CAACAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCACCAGGACTGGCTGAATGG CAAG GAGTACAAGTGCAAGGTCTCCAACAAAGCCCTCCCAGCCCCCATCGAGAAAACCATCTCC AAAG CCAAAGGGCAGCCCCGAGAACCACAGGTCTACACCCTGCCCCCATCCCGGGAGGAGATGA CCAA GAACCAGGTCAGCCTGTACTGCCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGA GTGG GAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCACGCCTCCCGTGCTGGACTCCGAC GGCT CCTTCTTCCTCTATAGCAAGCTCACCGTGGACAAGAGCAGGTGGCAGCAGGGGAACGTCT TCTC ATGCTCCGTGATGCATGAGGCTCTGCACAACCACTACACGCAGAAGAGCCTAAGCTTGTC TCCG GGTAAAGGAGGCGGAGGATCTGGCGGAGGTGGAAGTGGCGGAGGCGGATCTCAATCTGCT CTTA CACAGCCTGCCAGCGTGTCCGGATCTCCTGGCCAGAGCATCACCATCAGCTGTACCGGCA CCAG CTCTGATGTCGGCGGCTACAATTACGTGTCCTGGTATCAGCAGCACCCCGGCAAGGCCCC TAAG CTGATGATCTACGACGTGTCCAACAGACCCAGCGGCGTGTCCAATAGATTCTCCGGCAGC AAGA GCGGCAACACCGCCAGCCTGACAATTAGCGGACTGCAGGCCGAGGACGAGGCCGATTACT ACTG TAGCAGCTACACCAGCTCCAGCACCAGAGTGTTTGGCACCGGCACAAAAGTGACCGTGCT GGGC CAGCCTAAGGCCGGTGGAGGTGGGTCTGGAGGGGGTGGATCTGGAGGTGGCGGATCGGAG GTGC AGCTGCTGGAATCTGGCGGAGGACTTGTTCAGCCTGGCGGCTCTCTGAGACTGTCTTGTG CCGC CAGCGGCTTCACCTTCAGCAGCTATATCATGATGTGGGTCCGACAGGCCCCTGGCAAAGG CCTT GAATGGGTGTCCAGCATCTATCCCAGCGGCGGCATCACCTTTTACGCCGACACAGTGAAG GGCA GATTCACCATCAGCCGGGACAACAGCAAGAACACCCTGTACCTGCAGATGAACAGCCTGA GAGC CGAGGACACCGCCGTGTACTACTGCGCCAGAATCAAGCTGGGCACCGTGACCACCGTGGA TTAT TGGGGACAGGGCACCCTGGTCACCGTGTCATCT

[00452] SEQ ID NO: 112:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDAGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PI P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ

ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNP RPPAPEA

WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEY LPQGGGG

SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPE VKFNWY

VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTI SKAKGQ

PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLD SDGSFFL

TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00453] SEQ ID NO: 113 :

GATGCATCTCTGCCTTACCTGCAGAAAGAAAGCGTGTTCCAGTCTGGCGCCCACGCC TACAGAA TTCCCGCTCTGCTGTATCTGCCAGGCCAGCAGTCTCTGCTGGCTTTCGCTGAACAGCGGG CCAG CAAGAAGGATGAGCACGCCGAACTGATCGTGCTGCGGAGAGGCGATTACGACGCCGGCAC ACAT CAGGTGCAGTGGCAGGCTCAAGAGGTGGTGGCTCAGGCTAGACTGGACGGCCACAGATCT ATGA ACCCCTGTCCTCTGTACGATGAACAGACCGGCACACTGTTTCTGTTCTTTATCGCTATCC CCGG CCAAGTGACCGAGCAGCAGCAGCTGCAGACAAGAGCCAACGTGACCAGACTGTGTCAAGT GACC TCCACCGACCACGGCAGAACCTGGTCTAGCCCTAGAGATCTGACCGACGCCGCCATCGGA CCTG CCTATAGAGAGTGGTCCACCTTCGCCGTTGGACCTGGACACTGTCTCCAGCTGCACGACA GGGC TAGATCTCTGGTGGTGCCTGCCTACGCCTATAGAAAGCTGCACCCCAAACAGCGGCCTAT TCCT AGCGCCTTCTGCTTTCTGAGCCACGATCACGGCAGGACATGGGCCAGAGGACATTTCGTG GCCC AGGACACACTGGAATGCCAGGTGGCCGAAGTGGAAACCGGCGAGCAGAGAGTCGTGACCC TGAA CGCCAGATCTCACCTGAGAGCCAGAGTGCAGGCCCAGAGCACAAACGACGGCCTGGATTT CCAA GAGAGCCAGCTGGTCAAGAAACTGGTGGAACCTCCTCCACAGGGCTGTCAGGGAAGCGTG ATCA GCTTTCCATCTCCTAGAAGCGGCCCTGGCTCTCCTGCTCAGTGGCTGCTGTATACACACC CCAC ACACAGCTGGCAGAGAGCCGATCTGGGCGCCTACCTGAATCCTAGACCTCCTGCTCCTGA GGCT TGGAGCGAACCTGTTCTGCTGGCCAAGGGCAGCGCTGCCTACAGCGATCTGCAGTCTATG GGCA CAGGCCCTGATGGCAGCCCTCTGTTTGGCTGTCTGTACGAGGCCAACGACTACGAAGAGA TCGT GTTCCTGATGTTCACCCTGAAGCAGGCCTTTCCAGCCGAGTACCTGCCTCAAGGCGGAGG TGGA AGTGGCGGAGGCGGATCCGACAAAACTCACACATGCCCACCGTGCCCAGCACCTGAACTC CTGG GGGGACCGTCAGTCTTCCTCTTCCCCCCAAAACCCAAGGACACCCTCATGATCTCCCGGA CCCC TGAGGTCACATGCGTGGTGGTGGACGTGAGCCACGAAGACCCTGAGGTCAAGTTCAACTG GTAC GTGGACGGCGTGGAGGTGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTACAACAGC ACGT ACCGTGTGGTCAGCGTCCTCACCGTCCTGCACCAGGACTGGCTGAATGGCAAGGAGTACA AGTG CAAGGTCTCCAACAAAGCCCTCCCAGCCCCCATCGAGAAAACCATCTCCAAAGCCAAAGG GCAG CCCCGAGAACCACAGGTCTACACCCTGCCCCCATCCCGGGAGGAGATGACCAAGAACCAG GTCA GCCTGACCTGCCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAGTGGGAGAGCA ATGG GCAGCCGGAGAACAACTACAAGACCACGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTT CCTC ACTAGCAAGCTCACCGTGGACAAGAGCAGGTGGCAGCAGGGGAACGTCTTCTCATGCTCC GTGA TGCATGAGGCTCTGCACAACCACTACACGCAGAAGAGCCTCTCCCTGTCTCCGGGTAAA

[00454] SEQ ID NO: 114:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRG DYDAGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC QVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PI P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLY SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGKGGGGSGGGGSGGGGSQSALTQPAS VSGS PGQS ITISCTGTSSDVGGYNYVSWYQQHPGKAPKLMIYDVSNRPSGVSNRFSGSKSGNTASLTI SGLQAEDEADYYCSSYTSSSTRVFGTGTKVTVLGQPKAGGGGSGGGGSGGGGSEVQLLES GGGL VQPGGSLRLSCAASGFTFSSYIMMWVRQAPGKGLEWVSS IYPSGGITFYADTVKGRFTISRDNS KNTLYLQMNSLRAEDTAVYYCARIKLGTVTTVDYWGQGTLVTVSS

[00455] SEQ ID NO: 115:

GATGCATCTCTGCCTTACCTGCAGAAAGAAAGCGTGTTCCAGTCTGGCGCCCACGCC TACAGAA TTCCCGCTCTGCTGTATCTGCCAGGCCAGCAGTCTCTGCTGGCTTTCGCTGAACAGCGGG CCAG CAAGAAGGATGAGCACGCCGAACTGATCGTGCTGCGGAGAGGCGATTACGACGCCGGCAC ACAT CAGGTGCAGTGGCAGGCTCAAGAGGTGGTGGCTCAGGCTAGACTGGACGGCCACAGATCT ATGA ACCCCTGTCCTCTGTACGATGAACAGACCGGCACACTGTTTCTGTTCTTTATCGCTATCC CCGG CCAAGTGACCGAGCAGCAGCAGCTGCAGACAAGAGCCAACGTGACCAGACTGTGTCAAGT GACC TCCACCGACCACGGCAGAACCTGGTCTAGCCCTAGAGATCTGACCGACGCCGCCATCGGA CCTG CCTATAGAGAGTGGTCCACCTTCGCCGTTGGACCTGGACACTGTCTCCAGCTGCACGACA GGGC TAGATCTCTGGTGGTGCCTGCCTACGCCTATAGAAAGCTGCACCCCAAACAGCGGCCTAT TCCT AGCGCCTTCTGCTTTCTGAGCCACGATCACGGCAGGACATGGGCCAGAGGACATTTCGTG GCCC AGGACACACTGGAATGCCAGGTGGCCGAAGTGGAAACCGGCGAGCAGAGAGTCGTGACCC TGAA CGCCAGATCTCACCTGAGAGCCAGAGTGCAGGCCCAGAGCACAAACGACGGCCTGGATTT CCAA GAGAGCCAGCTGGTCAAGAAACTGGTGGAACCTCCTCCACAGGGCTGTCAGGGAAGCGTG ATCA GCTTTCCATCTCCTAGAAGCGGCCCTGGCTCTCCTGCTCAGTGGCTGCTGTATACACACC CCAC ACACAGCTGGCAGAGAGCCGATCTGGGCGCCTACCTGAATCCTAGACCTCCTGCTCCTGA GGCT TGGAGCGAACCTGTTCTGCTGGCCAAGGGCAGCGCTGCCTACAGCGATCTGCAGTCTATG GGCA CAGGCCCTGATGGCAGCCCTCTGTTTGGCTGTCTGTACGAGGCCAACGACTACGAAGAGA TCGT GTTCCTGATGTTCACCCTGAAGCAGGCCTTTCCAGCCGAGTACCTGCCTCAAGAGCCCAA ATCT TCTGACAAAACTCACACATGCCCACCGTGCCCAGCACCTGAACTCCTGGGGGGACCGTCA GTCT TCCTCTTCCCCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCCTGAGGTCACAT GCGT GGTGGTGGACGTGAGCCACGAAGACCCTGAGGTCAAGTTCAACTGGTACGTGGACGGCGT GGAG GTGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTACAACAGCACGTACCGTGTGGTC AGCG TCCTCACCGTCCTGCACCAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCTCCA ACAA AGCCCTCCCAGCCCCCATCGAGAAAACCATCTCCAAAGCCAAAGGGCAGCCCCGAGAACC ACAG GTCTACACCCTGCCCCCATCCCGGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTGC CTGG TCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAGTGGGAGAGCAATGGGCAGCCGGAGA ACAA CTACAAGACCACGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTATAGCAAGCT CACC GTGGACAAGAGCAGGTGGCAGCAGGGGAACGTCTTCTCATGCTCCGTGATGCATGAGGCT CTGC ACAACCACTACACGCAGAAGAGCCTAAGCTTGTCTCCGGGTAAAGGAGGCGGAGGATCTG GCGG AGGTGGAAGTGGCGGAGGCGGATCTCAATCTGCTCTTACACAGCCTGCCAGCGTGTCCGG ATCT CCTGGCCAGAGCATCACCATCAGCTGTACCGGCACCAGCTCTGATGTCGGCGGCTACAAT TACG TGTCCTGGTATCAGCAGCACCCCGGCAAGGCCCCTAAGCTGATGATCTACGACGTGTCCA ACAG ACCCAGCGGCGTGTCCAATAGATTCTCCGGCAGCAAGAGCGGCAACACCGCCAGCCTGAC AATT AGCGGACTGCAGGCCGAGGACGAGGCCGATTACTACTGTAGCAGCTACACCAGCTCCAGC ACCA GAGTGTTTGGCACCGGCACAAAAGTGACCGTGCTGGGCCAGCCTAAGGCCGGTGGAGGTG GGTC TGGAGGGGGTGGATCTGGAGGTGGCGGATCGGAGGTGCAGCTGCTGGAATCTGGCGGAGG ACTT GTTCAGCCTGGCGGCTCTCTGAGACTGTCTTGTGCCGCCAGCGGCTTCACCTTCAGCAGC TATA TCATGATGTGGGTCCGACAGGCCCCTGGCAAAGGCCTTGAATGGGTGTCCAGCATCTATC CCAG CGGCGGCATCACCTTTTACGCCGACACAGTGAAGGGCAGATTCACCATCAGCCGGGACAA CAGC AAGAACACCCTGTACCTGCAGATGAACAGCCTGAGAGCCGAGGACACCGCCGTGTACTAC TGCG CCAGAATCAAGCTGGGCACCGTGACCACCGTGGATTATTGGGGACAGGGCACCCTGGTCA CCGT GTCATCT [00456] SEQ ID NO: 116:

X1ASLPX2LQX3ESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVL RRGDYDAX4

THQVQWQAQEWAQARLDGHRSMNPCPLYDX ₅ QTGTLFLFFIAIPGQVTEQQQLQTRANVTRLCX

₆ VTSTDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAY RKLHPX ₇ QR

PIPSAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRXsRVQA QSTNDGL

DFQESQLVKKLVEPPPX ₉ GCQGSVISFPSPRSGPGSPAQWLLYTHPTHX ₁₀ X ₁₁ QRADLGAYLNPR

PPAPEAWSEPVLLAKGSX ₁₂ AYSDLQSMGTGPDGSPLFGCLYEANDYEEIX ₁₃ FX ₁₄ MFTLKQAFP

AEYLPQX ₁₅ DKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKF N

WYVDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEK TISKAK

GQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPV LDSDGSF

FLTSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00457] SEQ ID NO: 117:

X ₁ X ₂ SX ₃ X ₄ X ₅ LQX ₆ ESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASX ₇ X ₈ DEHAELIVX ₉ RRGD

YDAX10THQVQWX11AQEWAQAX12LX13GHRSMNPCPLYDX14QTGTLFLFFIAIP X15X16VTEX17

QQLQTRANVTRLX18X19VTSTDHGRTWSSPRDLTDAAIGPX20YREWSTFAVGPGH X21LQLHDX22

X ₂₃ RSLWPAYAYRKLHPX ₂₄ X ₂₅ X ₂₆ PIPSAFX ₂₇ FLSHDHGRTWARGHFVX ₂₈ QDTX ₂₉ ECQVAEVX

₃₀ TGEQRWTLNARSX ₃₁ X ₃₂ X ₃₃ X ₃₄ RX ₃₅ QAQSX ₃₆ NX ₃₇ GLDFQX ₃₈ X ₃₉ QX ₄₀ VKKL

X ₄₁ EPPPX ₄₂ GX ₄₃ QGSVISFPSPRSGPGSPAQX ₄₄ LLYTHPTHX ₄₅ X ₄₆ QRADLGAYLNPRPPAPEA

WSEPX ₄₇ LLAKGSX ₄₈ AYSDLQSMGTGPDGSPLFGX ₄₉ LYEANDYEEIX ₅₀ FX ₅₁ MFTLKQAFPAEYL

PQX ₅₂ DKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCWVDVSHEDPEVKF NWYVD

GVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISK AKGQPR

EPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSD GSFFLTS

KLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00458] SEQ ID NO: 118:

gatGCATCTCTGCCTTACCTGCAGAAAGAAAGCGTGTTCCAGTCTGGCGCCCACGCC TACAGAA TTCCCGCTCTGCTGTATCTGCCAGGCCAGCAGTCTCTGCTGGCTTTCGCTGAACAGCGGG CCAG CAAGAAGGATGAGCACGCCGAACTGATCGTGCTGCGGAGAGGCGATTACGACGCCggcAC ACAT CAGGTGCAGTGGCAGGCTCAAGAGGTGGTGGCTCAGGCTAGACTGGACGGCCACAGATCT ATGA ACCCCTGTCCTCTGTACGATgaaCAGACCGGCACACTGTTTCTGTTCTTTATCGCTATCC CCGG CCAAGTGACCGAGCAGCAGCAGCTGCAGACAAGAGCCAACGTGACCAGACTGTGTtacGT GACC TCCACCGACCACGGCAGAACCTGGTCTAGCCCTAGAGATCTGACCGACGCCGCCATCGGA CCTG CCTATAGAGAGTGGTCCACCTTCGCCGTTGGACCTGGACACTGTCTCCAGCTGCACGACA GGGC TAGATCTCTGGTGGTGCCTGCCTACGCCTATAGAAAGCTGCACCCCAAACAGCGGCCTAT TCCT AGCGCCTTCTGCTTTCTGAGCCACGATCACGGCAGGACATGGGCCAGAGGACATTTCGTG GCCC AGGACACACTGGAATGCCAGGTGGCCGAAGTGGAAACCGGCGAGCAGAGAGTCGTGACCC TGAA CGCCAGATCTCACCTGAGATTCAGAGTGCAGGCCCAGAGCACAAACGACGGCCTGGATTT CCAA GAGAGCCAGCTGGTCAAGAAACTGGTGGAACCTCCTCCAaccGGCTGTCAGGGAAGCGTG ATCA GCTTTCCATCTCCTAGAAGCGGCCCTGGCTCTCCTGCTCAGTGGCTGCTGTATACACACC CCAC ACACAGCTGGCAGAGAGCCGATCTGGGCGCCTACCTGAATCCTAGACCTCCTGCTCCTGA GGCT TGGAGCGAACCTGTTCTGCTGGCCAAGGGCAGCgctGCCTACAGCGATCTGCAGTCTATG GGCA CAGGCCCTGATGGCAGCCCTCTGTTTGGCTGTCTGTACGAGGCCAACGACTACGAAGAGA TCGT GTTCCTGATGTTCACCCTGAAGCAGGCCTTTCCAGCCGAGTACCTGCCTCAA [00459] SEQ ID NO: 119:

X ₁ X ₂ SX ₃ X ₄ X ₅ LQX ₆ ESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASX ₇ X ₈ DEHAELIVX ₉ RRGD

YDAX10THQVQWX11AQEWAQAX12LX13GHRSMNPCPLYDX14QTGTLFLFFIAIP X15X16VTEX17

QQLQTRANVTRLX18X19VTSTDHGRTWSSPRDLTDAAIGPX20YREWSTFAVGPGH X21LQLHDX22

X ₂₃ RSLWPAYAYRKLHPX ₂₄ X ₂₅ X ₂₆ PIPSAFX ₂₇ FLSHDHGRTWARGHFVX ₂₈ QDTX ₂₉ ECQVAEVX

₃₀ TGEQRWTLNARSX ₃₁ X ₃₂ X ₃₃ X ₃₄ RX ₃₅ QAQSX ₃₆ NX ₃₇ GLDFQX ₃₈ X ₃₉ QX ₄₀ VKKL

X ₄₁ EPPPX ₄₂ GX ₄₃ QGSVISFPSPRSGPGSPAQX ₄₄ LLYTHPTHX ₄₅ X ₄₆ QRADLGAYLNPRPPAPEA

WSEPX ₄₇ LLAKGSX ₄₈ AYSDLQSMGTGPDGSPLFGX ₄₉ LYEANDYEEIX ₅₀ FX ₅₁ MFTLKQAFPAEYL

PQ

[00460] SEQ ID NO: 120:

X1ASLPX2LQX3ESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVL RRGDYDAX4

THQVQWQAQEWAQARLDGHRSMNPCPLYDX ₅ QTGTLFLFFIAIPGQVTEQQQLQTRANVTRLCX

₆ VT STDHGRTWSS PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPX ₇ QR

PIPSAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRXsRVQA QSTNDGL

DFQESQLVKKLVEPPPX ₉ GCQGSVISFPSPRSGPGSPAQWLLYTHPTHX ₁₀ X ₁₁ QRADLGAYLNPR

PPAPEAWSEPVLLAKGSX ₁₂ AYSDLQSMGTGPDGSPLFGCLYEANDYEEIX ₁₃ FX ₁₄ MFTLKQAFP

AEYLPQ

[00461] SEQ ID NO: 121:

GGGGS

[00462] SEQ ID NO: 122:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC YVT STDHGRTWSS PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPKQRP I P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPTGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLYCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLY SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00463] SEQ ID NO 123:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC YVT STDHGRTWSS PRDLTDAAI GPAYREWS T FAVGPGHCLQLHDRARS LWPAYAYRKLHPKQRP I P SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRFRVQAQSTNDGL DFQ ESQLVKKLVEPPPTGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLYCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLY SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK [00464] SEQ ID NO: 124:

EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYIMMWVRQAPGKGLEWVSS IYPSGGITFYADTV KGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARIKLGTVTTVDYWGQGTLVTVSSASTK GPSV FPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSW TVP SSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKD TLMI SRTPEVTCVWDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLN GK EYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDI AVEW ESNGQPENNYKTTPPVLDSDGSFFLTSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSL SLSP GK

[00465] SEQ ID NO: 125:

QSALTQPASVSGSPGQSITISCTGTSSDVGGYNYVSWYQQHPGKAPKLMIYDVSNRPSGV SNRF SGSKSGNTASLTISGLQAEDEADYYCSSYTSSSTRVFGTGTKVTVLGQPKAGGGGSGGGG SGGG GSEVQLLESGGGLVQPGGSLRLSCAASGFTFSSYIMMWVRQAPGKGLEWVSS IYPSGGITFYAD TVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARIKLGTVTTVDYWGQGTLVTVSS

[00466] SEQ ID NO: 126:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC YVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ

[00467] SEQ ID NO: 127:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC YVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ EPKS SDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCWVDVSHEDPEVKFNWYVD GVE VHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPR EPQ VYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLT SKLT VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

[00468] SEQ ID NO 128:

DASLPYLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD AGTH QVQWQAQEWAQARLDGHRSMNPCPLYDEQTGTLFLFFIAIPGQVTEQQQLQTRANVTRLC YVT STDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLWPAYAYRKLHPKQR PIP SAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRWTLNARSHLRARVQAQSTNDGL DFQ ESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTHSWQRADLGAYLNPRPP APEA WSEPVLLAKGSAAYSDLQSMGTGPDGSPLFGCLYEANDYEEIVFLMFTLKQAFPAEYLPQ GGGG SGGGGSDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVWDVSHEDPEVKF NWY VDGVEVHNAKTKPREEQYNSTYRWSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKA KGQ PREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFL TSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK