METHODS OF TREATING GLUCOSE METABOLISM DISORDERS

CROSS-REFERENCE TO RELATED APPLICATION

[0001] This application claims priority benefit of U.S. provisional application serial no.

61.672,667, filed July 17, 2012, which application is incorporated herein by reference in its entirety.

INTRODUCTION

[0002] High blood glucose levels stimulate the secretion of insulin by pancreatic beta- cells. Insulin in turn stimulates the entry of glucose into muscles and adipose cells, leading to the storage of glycogen and triglycerides and to the synthesis of proteins. Activation of insulin receptors on various cell types diminishes circulating glucose levels by increasing glucose uptake and utilization, and by reducing hepatic glucose output. Disruptions within this regulatory network can result in diabetes and associated pathologic syndromes that affect a large and growing percentage of the human population.

[0003] Patients who have a glucose metabolism disorder can suffer from hyperglycemia, hyperinsulinemia, and/or glucose intolerance. An example of a disorder that is often associated with the aberrant levels of glucose and/or insulin is insulin resistance, in which liver, fat, and muscle cells lose their ability to respond to normal blood insulin levels.

[0004] In view of the prevalence and severity of diabetes and associated metabolic and non-metabolic disorders, along with the shortcomings of current treatment options, alternative treatment modalities that modulate glucose and/or insulin levels and enhance the biological response to fluctuating glucose levels in a patient remain of interest.

SUMMARY

[0005] The present disclosure contemplates the use of the agents described herein, and compositions thereof, to treat and/or prevent various diseases, disorders and conditions, and/or the symptoms thereof. In some embodiments, the diseases, disorders and conditions, and/or the symptoms thereof, pertain to metabolic-related disorders, while in other embodiments they pertain to glucose metabolism disorders. By way of example, but not limitation, the agents, and compositions thereof, can be used for the treatment and/or prevention of diabetes (e.g., Type 2 diabetes), insulin resistance and diseases, disorders and conditions characterized by insulin resistance, decreased insulin production, hyperglycemia, hypoinsulinemia, and metabolic syndrome. The agents, and compositions thereof, may also be useful in, for example, subjects who may be overweight or obese. As discussed further below, the agents of the present disclosure are referred to herein as "Modulators".

[0006] As described herein, peptide subsequences derived from the Ednl, Habp2,

Kazaldl, Respl8, and Tinag gene product have been identified. While an understanding of all of the characteristics of these murine peptides and these human peptides is not required, they are believed to be secreted peptides.

[0007] In addition to the Ednl-, Habp2-, Kazaldl-, Respl8-, and Tinag-related human and murine peptides described above and the Ednl-, Habp2-, Kazaldl-, Respl8-, and Tinag- related nucleic acid sequences that encode them, the present disclosure contemplates

homologues, variants, fragments and other modified forms thereof. For the sake of convenience, the aforementioned human peptides and homologous and variants thereof are collectively referred to hereafter as the "Human Peptides"; the aforementioned murine peptides and homologous and variants thereof are collectively referred to hereafter as the "Murine Peptides"; the aforementioned human nucleic acids and homologous and variants thereof are collectively referred to hereafter as the "Human Nucleic Acid Molecules"; and the aforementioned murine nucleic acids and homologous and variants thereof are collectively referred to as the "Murine Nucleic Acid Molecules". It should be noted that reference to "human" or "mouse" in connection with polypeptides, peptides and nucleic acid molecules of the present disclosure is not meant to be limiting with respect to the manner in which the peptide or nucleic acid is obtained or the source, but rather is only with reference to the sequence as it may correspond to a sequence of a naturally occurring human or mouse polypeptide or nucleic acid molecule. Furthermore, the Human Peptides and the Murine Peptides may be collectively referred to as the "Peptides", while the Human Nucleic Acid Molecules and the Murine Nucleic Acid Molecules may be collectively referred to as the "Nucleic Acid Molecules". Hereafter, unless otherwise indicated, reference to Ednl-, Habp2-, Kazaldl-, Respl8-, and Tinag-related peptides is meant to refer to both the Human Peptides and the Murine Peptides. In addition to the Peptides, the present disclosure also contemplates Ednl-, Habp2-, Kazaldl-, Respl8-, and Tinag-related peptides, and the nucleic acid molecules which encode them, from other species (e.g., non-human primates (e.g., chimpanzees), dogs, rats, etc.). [0008] The present disclosure relates to both "Inhibitors" (as defined hereafter) and

"Activators" (as defined hereafter) of the Peptides. The term "Inhibitors" refers to agents that, for example, partially or totally block stimulation, decrease, prevent, delay activation, inactivate, desensitize, or down-regulate the function or activity of one or more Peptides, such as, for example, antagonists including antibodies, small molecule antagonist compounds, and antagonistic peptides structurally distinguishable from the peptides disclosed herein; other examples of Inhibitors are described below. The term "Activators" refers to agents that, for example, stimulate, increase, activate, facilitate, enhance activation, sensitize or up-regulate the function or activity of one or more Peptides, such as, for example, agonists including antibodies, small molecule agonist compounds, the peptides disclosed herein, and other agonistic peptides structurally distinguishable from the peptides disclosed herein; other examples of Activators are described below. Hereafter, Inhibitors and Activators are collectively referred to as

"Modulators".

[0009] In one embodiment, compositions are provided that comprise one or more peptides or antibodies of the present disclosure, which compositions are useful in treating or preventing a metabolic disorder. In some embodiments, the compositions modulate aberrant glucose and/or insulin levels in a subject and may be used to treat or prevent diabetes mellitus (e.g., Type I and Type II diabetes and gestational diabetes). The compositions comprising the peptides described herein may also be used to treat, for example, insulin resistance,

hyperinsulinemia, glucose intolerance, hyperglycemia or metabolic syndrome, and may also be used to treat or prevent various body weight - related disorders (e.g., obesity).

[0010] In another embodiment, a use or method of treatment of a subject includes administering a Peptide to a subject, such as a subject having, or at risk of having, a disease or disorder treatable by a Peptide, in an amount effective for treating the disease or disorder. In a further embodiment, a method includes administering a Peptide to a subject, such as a subject having a hyperglycemic condition, insulin resistance, hyperinsulinemia, glucose intolerance or metabolic syndrome, in an amount effective for treating the disease or disorder.

[0011] Other aspects of the present disclosure include cell-based expression systems, vectors, engineered cell lines, and methods and uses related to the foregoing.

[0012] As described in detail hereafter, one embodiment of the present disclosure relates to a peptide comprising any one of: a subsequence of human Ednl or a murine isoform of Ednl as depicted in Figure 4, or a variant thereof; or the sequence CWXFCQA (SEQ ID NO: 36), where X is a semi-conserved residue. In some cases, X is N or T. In some cases, the peptide comprises a carboxyl-terminal modification, e.g., instead of a carboxyl group at the carboxyl terminus, the peptide comprises a CONH ₂ group.

[0013] In other embodiments, the peptide comprises a variant of a human Ednl peptide of Figure 2, a variant of a murine Ednl peptide of Figure 3 A, or a variant of the highlighted Ednl subsequence shown in Figure 2 or Figure 3A. In still further embodiments, the variant of a human Ednl peptide comprises an amino acid sequence having at least 85% amino acid identity, at least 90% amino acid identity, at least 93% amino acid identity, at least 95% amino acid identity, at least 97% amino acid identity, at least 98% amino acid identity, or at least 99% amino acid identity to the amino acid sequence of a human Ednl peptide of Figure 2, or the highlighted subsequence shown in Figure 2.

[0014] In still other embodiments, the Ednl peptide comprises the amino acid sequence

CWXFCQA (SEQ ID NO: 36), where X is as defined above, and has fewer than 100 amino acid residues, fewer than 75 amino acid residues, fewer than 50 amino acid residues, fewer than 25 amino acid residues, or fewer than 20 amino acid residues. In some embodiments, the Ednl peptide comprises the amino acid sequence CWXFCQA comprising a CONH ₂ group instead of a COOH group at the carboxyl terminus of the peptide.

[0015] As described in detail hereafter, one embodiment of the present disclosure relates to a peptide comprising any one of: a subsequence of human Habp2 or a murine isoform of Habp2 as depicted in Figure 9, or a variant thereof; or the sequence

PGVYTQVX1KFLNWIKX2TX3X4X5X6X7X8X9 (SEQ ID NO: 37), where each of X1-X9 are semi-conserved residues. In some cases, Xi and X ₂ are A or T; X ₃ is I or M; X ₄ is K, Q, or H; X ₅ is S, K, or R; X ₆ is E or G; X ₇ is S or A; X ₈ is S or G; and X is F or L. In some cases, the peptide comprises a carboxyl-terminal modification, e.g., instead of a carboxyl group at the carboxyl terminus, the peptide comprises a CONH ₂ group.

[0016] In other embodiments, the peptide comprises a variant of a human Habp2 peptide of Figure 7a, a variant of a murine Habp2 peptide of Figure 8a, or a variant of the highlighted Habp2 subsequence shown in Figure 7a or Figure 8a. In still further embodiments, the variant of a human Habp2 peptide comprises an amino acid sequence having at least 85% amino acid identity, at least 90% amino acid identity, at least 93% amino acid identity, at least 95% amino acid identity, at least 97% amino acid identity, at least 98%> amino acid identity, or at least 99% amino acid identity to the amino acid sequence of a human Habp2 peptide of Figure 7a, or the highlighted subsequence shown in Figure 7a.

[0017] In still other embodiments, the Habp2 peptide comprises the amino acid sequence

PGVYTQVX1KFLNWIKX2TX3X4X5X6X7X8X9 (SEQ ID NO: 37), where X1-X9 are as defined above, and has fewer than 100 amino acid residues, fewer than 75 amino acid residues, fewer than 50 amino acid residues, fewer than 25 amino acid residues, or fewer than 20 amino acid residues. In some embodiments, the Habp2 peptide comprises the amino acid sequence

PGVYTQVX1KFLNWIKX2TX3X4X5X6X7X8X9 (SEQ ID NO: 37) comprising a CONH ₂ group instead of a COOH group at the carboxyl terminus of the peptide.

[0018] As described in detail hereafter, one embodiment of the present disclosure relates to a peptide comprising any one of: a subsequence of human Kazaldl or a murine isoform of Kazaldl as depicted in Figure 13B, or a variant thereof; or the sequence

GWX ₁ RLLAEGEGCAPCRPEX ₂ CAAPRGCLA (SEQ ID NO: 38), where Xi and X ₂ are semi- conserved residues. In some embodiments, XI is L or M and X2 is E or D. In some cases, the peptide comprises a carboxyl-terminal modification, e.g., instead of a carboxyl group at the carboxyl terminus, the peptide comprises a CONH2 group.

[0019] In other embodiments, the peptide comprises a variant of a human Kazaldl peptide of Figure 12 A, a variant of a murine Kazaldl peptide of Figure 13 A, or a variant of the highlighted Kazaldl subsequence shown in Figure 12A or Figure 13 A. In still further embodiments, the variant of a human Kazaldl peptide comprises an amino acid sequence having at least 85% amino acid identity, at least 90%> amino acid identity, at least 93% amino acid identity, at least 95% amino acid identity, at least 97% amino acid identity, at least 98% amino acid identity, or at least 99% amino acid identity to the amino acid sequence of a human Kazaldl peptide of Figure 12A, or the highlighted subsequence shown in Figure 12A.

[0020] In still other embodiments, the Kazaldl peptide comprises the amino acid sequence GWXiRLLAEGEGCAPCRPEX ₂ CAAPRGCLA (SEQ ID NO: 38), where Xi and X ₂ are as defined above, and has fewer than 100 amino acid residues, fewer than 75 amino acid residues, fewer than 50 amino acid residues, fewer than 25 amino acid residues, or fewer than 20 amino acid residues. In some embodiments, the Kazaldl peptide comprises the amino acid sequence GWXiRLLAEGEGCAPCRPEX ₂ CAAPRGCLA (SEQ ID NO: 38) comprising a CONH ₂ group instead of a COOH group at the carboxyl terminus of the peptide.

[0021] As described in detail hereafter, one embodiment of the present disclosure relates to a peptide comprising any one of: a subsequence of human Respl8 or a murine isoform of Respl8 as depicted in Figure 18; or the sequence

XiX ₂ CFTX3X4VX5X6KX ₇ X8X9XioXiiXi2Xi3Xi4P(X)n (SEQ ID NO: 39), where X1-X5, X7-X12, and X ₁₄ are semi-conserved residues; where X ₆ is P, L, or S; where X ₁₃ is T, K, or A; where X ₁₄ is H, T, or N; and where n is an integer from 1 to 5 (e.g., 1, 2, 3, 4, or 5) and X is any amino acid. In some embodiments, Xi is D or E; X ₂ is R or Q; X ₃ is T or S; X ₄ is or E; X ₅ is I, D, or V; X ₇ is A or T; X ₈ is T or L; X is K or E; X ₁₀ is I or Q; Xn is E or H; and X ₁₂ is A, V, or I. In some cases, (X)n can be T, S, IV, or VKITY (SEQ ID NO: 40). In some cases, the peptide comprises a carboxyl-terminal modification, e.g., instead of a carboxyl group at the carboxyl terminus, the peptide comprises a CONH ₂ group.

[0022] In other embodiments, the peptide comprises a variant of a human Respl8 peptide of Figure 16, a variant of a murine Respl8 peptide of Figure 17, or a variant of the highlighted Respl8 subsequence shown in Figure 16 or Figure 17. In still further embodiments, the variant of a human Respl8 peptide comprises an amino acid sequence having at least 85% amino acid identity, at least 90% _> amino acid identity, at least 93% amino acid identity, at least 95% amino acid identity, at least 97% amino acid identity, at least 98% amino acid identity, or at least 99% amino acid identity to the amino acid sequence of a human Respl8 peptide of Figure 16, or the highlighted subsequence shown in Figure 16.

[0023] In still other embodiments, the Respl8 peptide comprises the amino acid sequence XiX ₂ CFTX ₃ X ₄ VX ₅ X6KX ₇ X ₈ X9XioXiiXi ₂ Xi3Xi4P(X)n (SEQ ID NO: 39), where X X ₁₄ and (X)n are as defined above, and has fewer than 100 amino acid residues, fewer than 75 amino acid residues, fewer than 50 amino acid residues, fewer than 25 amino acid residues, or fewer than 20 amino acid residues. In some embodiments, the Respl8 peptide comprises the amino acid sequence XiX ₂ CFTX ₃ X ₄ VX ₅ X6KX ₇ X ₈ X ₉ XioXiiXi ₂ Xi ₃ Xi4P(X)n (SEQ ID NO: 39) comprising a CONH ₂ group instead of a COOH group at the carboxyl terminus of the peptide.

[0024] As described in detail hereafter, one embodiment of the present disclosure relates to a peptide comprising any one of: a subsequence of human Tinag or a murine isoform of Tinag as depicted in Figure 23, or a variant thereof; or the sequence LX ₁ THAVKLTGWGTLX ₂ GAX3GX ₄ KEKFWIAANSWG (SEQ ID NO: 41), where X _h X ₂ , X ₃ , and X ₄ are semi-conserved residues. In some embodiments, each of Xi, X ₂ , X ₃ , and X4 is independently R, Q, or K. In some cases, Xi is R or Q; X ₂ is R or K; X3 is R or Q; and X ₄ is Q or K. In some cases, the peptide comprises a carboxyl-terminal modification, e.g., instead of a carboxyl group at the carboxyl terminus, the peptide comprises a CONH ₂ group. In some embodiments, the peptide comprises one of the following sequences:

LQTHAVKLTGWGTLRGAQGQKEKFWIAANSWG-COOH (SEQ ID NO: 42);

LQTHAVKLTGWGTLRGAQGQKEKFWIAANSW-CONH ₂ (SEQ ID NO: 43);

LRTHAVKLTGWGTLRGARGKKEKFWIAANSWG-COOH (SEQ ID NO: 44); or

LRTHAVKLTGWGTLRGARGKKEKFWIAANSW-CONH ₂ (SEQ ID NO: 45).

[0025] In other embodiments, the peptide comprises a variant of a human Tinag peptide of Figure 21, a variant of a murine Tinag peptide of Figure 22, or a variant of the highlighted Tinag subsequence shown in Figure 21 or Figure 22. In still further embodiments, the variant of a human Tinag peptide comprises an amino acid sequence having at least 85% amino acid identity, at least 90% amino acid identity, at least 93% amino acid identity, at least 95% amino acid identity, at least 97% amino acid identity, at least 98% amino acid identity, or at least 99% amino acid identity to the amino acid sequence of a human Tinag peptide of Figure 21, or the highlighted subsequence shown in Figure 21.

[0026] In still other embodiments, the Tinag peptide comprises the amino acid sequence

LX ₁ THAVKLTGWGTLX ₂ GAX3GX ₄ KEKFWIAANSWG (SEQ ID NO: 41), where X1-X4 and (X) _n are as defined above, and has fewer than 100 amino acid residues, fewer than 75 amino acid residues, fewer than 50 amino acid residues, fewer than 25 amino acid residues, or fewer than 20 amino acid residues. In some embodiments, the Tinag peptide comprises the amino acid sequence LXiTHAVKLTGWGTLX ₂ GAX ₃ GX ₄ KEKFWIAANSWG (SEQ ID NO: 41) comprising a CONH ₂ group instead of a COOH group at the carboxyl terminus of the peptide.

[0027] According to the present disclosure, the peptide may be isolated.

[0028] Furthermore, the present disclosure contemplates nucleic acid molecules encoding the aforementioned peptides. In some embodiments, a nucleic acid molecule is operably linked to an expression control element that confers expression of the nucleic acid molecule encoding the peptide in vitro, in a cell or in vivo. In some embodiments, a vector (e.g., a viral vector) contains one or more of the nucleic acid molecules.

[0029] Some embodiments include transformed or host cells that express one or more of the aforementioned peptides.

[0030] In particular embodiments of the present disclosure, one or more of the aforementioned peptides is formulated to yield a pharmaceutical composition, wherein the composition also includes one or more pharmaceutically acceptable diluents, carriers or excipients. In certain embodiments, a pharmaceutical composition also includes at least one additional prophylactic or therapeutic agent.

[0031] Still further embodiments of the present disclosure comprise an antibody that binds specifically to one of the aforementioned peptides. In some embodiments, the antibody comprises a light chain variable region and a heavy chain variable region present in separate polypeptides or in a single polypeptide. An antibody of the present disclosure binds the peptide with an affinity of from about 10 ⁷ M ^"1 to about 10 ¹² M ^"1 in certain embodiments. In still other embodiments, the antibody comprises a heavy chain constant region of the isotype IgGl, IgG2, IgG3, or IgG4. In additional embodiments, the antibody is detectably labeled, while it is a Fv, scFv, Fab, F(ab')2, or Fab' in other embodiments.

[0032] The present disclosure also contemplates antibodies that comprise a covalently linked non-peptide polymer (e.g., a poly(ethylene glycol) polymer). In other embodiments, the antibody comprises a covalently linked moiety selected from a lipid moiety, a fatty acid moiety, a polysaccharide moiety, and a carbohydrate moiety.

[0033] The antibody is a single chain Fv (scFv) antibody in some embodiments, and the scFv is multimerized in others.

[0034] The antibodies of the present disclosure may be, but are not limited to, monoclonal antibodies, polyclonal antibodies, or humanized antibodies.

[0035] Furthermore, the present disclosure contemplates pharmaceutical compositions comprising an antibody as described above formulated with at least one pharmaceutically acceptable excipient, carrier or diluent. Such pharmaceutical compositions may also contain at least one additional prophylactic or therapeutic agent.

[0036] Certain embodiments of the present disclosure contemplate a sterile container that contains one of the above-mentioned pharmaceutical compositions and optionally one or more additional components. By way of example, but not limitation, the sterile container may be a syringe. In still further embodiments, the sterile container is one component of a kit; the kit may also contain, for example, a second sterile container that contains at least one prophylactic or therapeutic agent.

[0037] The present disclosure also contemplates a method of treating or preventing a glucose metabolism disorder in a subject (e.g., a human) by administering to the subject a therapeutically effective amount of an Inhibitor (as defined herein). In certain embodiments, the Inhibitor is an antibody as described above, a small molecule antagonist compound, or an antagonistic peptide. In some methods, the treating or preventing results in a reduction in plasma glucose in the subject, a reduction in plasma insulin in the subject, or an increase in glucose tolerance in the subject. In particular embodiments, the glucose metabolism disorder is diabetes mellitus. In some embodiments, the subject is obese.

[0038] Furthermore, the present disclosure contemplates a method of treating or preventing a glucose metabolism disorder in a subject (e.g., a human) by administering to the subject a therapeutically effective amount of an Activator (as defined herein). The Activator may be, for example, one of the aforementioned peptides, a small molecule agonist compound, an agonistic peptide distinguishable from the peptides described herein, or an antibody.

[0039] Though not limited to any particular route of administration or dosing regimen, in some embodiments the administering is by parenteral (e.g., subcutaneous) injection.

BRIEF DESCRIPTION OF THE DRAWINGS

[0040] Figure 1 shows Ednl gene expression in enteroendocrine cells (EECs) and enterocytes (ECs) isolated from the indicated segments of the mouse gastrointestinal tract.

Hatched bars represent expression in EECs, while solid bars, if present, represent expression in ECs.

[0041] Figure 2 provides the full-length amino acid sequence of human Ednl (SEQ ID

NO: l) (the region encompassing the human Ednl human peptide [Human Peptide-pl] is highlighted in gray), and the nucleotide sequence encoding full-length human Ednl (SEQ ID NO: 2) (the coding region is highlighted in gray).

[0042] Figures 3A and 3B provide the full-length amino acid sequence (Figure 3A) of mouse Ednl (SEQ ID NO: 3) (the region encompassing the mouse Ednl peptide [Murine Peptide- l] is highlighted in gray), and the nucleotide sequence (Figure 3B) encoding full-length mouse Ednl (SEQ ID NO: 4) (the coding region is highlighted in gray).

[0043] Figure 4 shows a sequence alignment of Ednl amino acid sequences from the indicated species. Amino acid sequences from mouse (SEQ ID NO: 3), rat (SEQ ID NO: 5), dog (SEQ ID NO: 6), chimpanzee (SEQ ID NO: 7), and human (SEQ ID NO: l),comprising the Ednl - related peptides are highlighted in gray. Residue positions that are fully conserved are indicated by (*), whereas residue positions that are semi-conserved are indicated by (.).

[0044] Figure 5, Panel a shows the effect of a single, bolus i.p. injection of mouse Ednl

[Murine Peptide-pl] (10 mg/kg; gray squares) or Vehicle control (black squares) on basal (fasted) plasma glucose (FPG) concentration and oral glucose tolerance in high-fat fed mice. FPG concentrations were determined in untreated mice following a 4-hour fast (min-30).

Thereafter, mice received a single bolus i.p. injection of Murine Peptide-pl or Vehicle control, and at minO glucose (lg/kg) in phosphate buffered saline (PBS) was administered orally. Plasma glucose concentrations were determined at -30, 0, 15, 60 and 120 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[0045] Figure 5, Panel b shows the data from Figure 5, Panel a expressed as the percent change in plasma glucose concentration normalized to basal glucose concentration (min-30) following a single, bolus i.p. injection of mouse Ednl [Murine Peptide-pl] (10 mg/kg; gray squares) or Vehicle control (black squares) in high-fat fed mice, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[0046] Figure 5, Panel c shows the effect of a single, bolus i.p. injection of mouse Ednl

[Murine Peptide-pl] (10 mg/kg; gray squares) and Vehicle control (black squares) on basal (fasted) plasma insulin concentration (FPI) and on glucose-stimulated insulin secretion (GSIS) in high-fat fed mice. FPI concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Murine Peptide-pl or Vehicle control, and at minO glucose (lg/kg) in PBS was administered orally. Plasma insulin

concentrations were determined at -30, 0, 15, and 60 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.) [0047] Figure 5, Panel d shows the data from Figure 5, Panel c expressed as the percent change in plasma insulin concentration normalized to baseline (min-30) following a single, bolus i.p. injection of mouse Ednl [Murine Peptide -pi] (10 mg/kg; gray squares) or Vehicle control (black squares) in high-fat fed mice, (n = 6 mice per group; p-values determined by a student's t- test comparing Murine Peptide-pl and Vehicle-treated mice are indicated below the bars.)

[0048] Figure 6 shows Habp2 gene expression in EECs and ECs isolated from the indicated segments of the mouse gastrointestinal tract. Hatched bars represent expression in EECs, while solid bars, if present, represent expression in ECs.

[0049] Figures 7A and 7B provide the full-length amino acid sequence (Figure 7A) of human Habp2 (SEQ ID NO: 8) (the region encompassing the human Habp2 peptide [Human Peptide-pl] is highlighted in gray), and the nucleotide sequence (Figure 7B) encoding full-length human Habp2 (SEQ ID NO: 9) (the coding region is highlighted in gray).

[0050] Figures 8A and 8B provide the full-length amino acid sequence (Figure 8A) of mouse Habp2 ((SEQ ID NO: 10) the region encompassing the mouse Habp2 peptide [Mouse Peptide-pl] is highlighted in gray), and the nucleotide sequence (Figure 8B) encoding full-length mouse Habp2 (SEQ ID NO: 11) (the coding region is highlighted in gray).

[0051] Figure 9 shows a sequence alignment of Habp2 amino acid sequences from the indicated species. Amino acid sequences from chimpanzee (SEQ ID NO: 12), human (SEQ ID NO: 8), dog (SEQ ID NO: 13), mouse (SEQ ID NO: 10), and rat (SEQ ID NO: 14) comprising the Habp2 - related peptides are highlighted in gray. Residue positions that are fully conserved are indicated by (*), whereas residue positions that are semi-conserved are indicated by (.).

[0052] Figure 10, Panel a shows the effect of a single, bolus i.p. injection of mouse

Habp2 [Murine Peptide-pl] (10 mg/kg; gray squares) or Vehicle control (black squares) on basal (fasted) plasma glucose (FPG) concentration and oral glucose tolerance in high-fat fed mice. FPG concentrations were determined in untreated mice following a 4-hour fast (min-30).

Thereafter, mice received a single bolus i.p. injection of Murine Peptide-pl or Vehicle control, and at minO glucose (lg/kg) in PBS was administered orally. Plasma glucose concentrations were determined at -30, 0, 15, 60 and 120 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.) [0053] Figure 10, Panel b shows the data from Figure 10, Panel a expressed as the percent change in plasma glucose concentration normalized to basal glucose concentration (min- 30) following a single, bolus i.p. injection of mouse Habp2 [Murine Peptide-pl] (10 mg/kg; gray squares) or Vehicle control (black squares) in high-fat fed mice, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[0054] Figure 10, Panel c shows the effect of a single, bolus i.p. injection of mouse

Habp2 [Murine Peptide-pl] (10 mg/kg; gray squares) and Vehicle control (black squares) on basal (fasted) plasma insulin concentration (FPI) and on glucose-stimulated insulin secretion (GSIS) in high-fat fed mice. FPI concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Murine Peptide-pl or Vehicle control, and at minO glucose (lg/kg) in PBS was administered orally. Plasma insulin concentrations were determined at -30, 0, 15, and 60 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[0055] Figure 10, Panel d shows the data from Figure 10, Panel c expressed as the percent change in plasma insulin concentration normalized to baseline (min-30) following a single, bolus i.p. injection of mouse Habp2 [Murine Peptide-pl] (10 mg/kg; gray squares) or Vehicle control (black squares) in high- fat fed mice, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated below the bars.)

[0056] Figure 11 shows Kazaldl gene expression in EECs and ECs isolated from the indicated segments of the mouse gastrointestinal tract. Hatched bars represent expression in EECs, while solid bars, if present, represent expression in ECs.

[0057] Figures 12A and 12B provide the full-length amino acid sequence (Figure 12 A) of human Kazaldl (SEQ ID NO: 15) (the region encompassing the human Kazaldl peptide [Human Peptide-pl] is highlighted in gray), and the nucleotide sequence (Figure 12B) encoding full- length human Kazaldl (SEQ ID NO: 16) (the coding region is highlighted in gray).

[0058] Figure 13A provides the full-length amino acid sequence of mouse Kazaldl (the region encompassing the mouse Kazaldl peptide (SEQ ID NO: 17) [Mouse Peptide-pl] is highlighted in gray), and the nucleotide sequence encoding full-length mouse Kazaldl (SEQ ID NO: 18) (the coding region is highlighted in gray).

[0059] Figure 13B shows a sequence alignment of Kazaldl amino acid sequences from the indicated species. Amino acid sequences from mouse (SEQ ID NO: 17), rat (SEQ ID NO: 19), chimpanzee (SEQ ID NO: 20), human (SEQ ID NO: 15), and dog (SEQ ID NO: 21) comprising the Kazaldl - related peptides are highlighted in gray. Residue positions that are fully conserved are indicated by (*), whereas residue positions that are semi-conserved are indicated by (.). The regions encompassing the Kazaldl Peptides are highlighted in gray.

[0060] Figure 14, Panel a shows the effect of a single, bolus i.p. injection of mouse

Kazaldl [Murine Peptide-pl] (10 mg/kg; gray squares) or Vehicle control (black squares) on basal (fasted) plasma glucose (FPG) concentration and oral glucose tolerance in high-fat fed mice. FPG concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Murine Peptide-pl or Vehicle control, and at minO glucose (lg/kg) in PBS was administered orally. Plasma glucose concentrations were determined at -30, 0, 15, 60 and 120 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[0061] Figure 14, Panel b shows the data from Figure 14, Panel a expressed as the percent change in plasma glucose concentration normalized to basal glucose concentration (min- 30) following a single, bolus i.p. injection of mouse Kazaldl [Murine Peptide-pl] (10 mg/kg; gray squares) or Vehicle control (black squares) in high-fat fed mice, (n = 6 mice per group; p- values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[0062] Figure 14, Panel c shows the effect of a single, bolus i.p. injection of mouse

Kazaldl [Murine Peptide-pl] (10 mg/kg; gray squares) and Vehicle control (black squares) on basal (fasted) plasma insulin concentration (FPI) and on glucose-stimulated insulin secretion (GSIS) in high-fat fed mice. FPI concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Murine Peptide-pl or Vehicle control, and at minO glucose (lg/kg) in PBS was administered orally. Plasma insulin concentrations were determined at -30, 0, 15, and 60 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[0063] Figure 14, Panel d shows the data from Figure 14, Panel c expressed as the percent change in plasma insulin concentration normalized to baseline (min-30) following a single, bolus i.p. injection of mouse Kazaldl [Murine Peptide-pl] (10 mg/kg; gray squares) or Vehicle control (black squares) in high- fat fed mice, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated below the bars.)

[0064] Figure 15 shows Respl8 gene expression in EECs and ECs isolated from the indicated segments of the mouse gastrointestinal tract. Hatched bars represent expression in EECs, while solid bars, if present, represent expression in ECs.

[0065] Figure 16 provides the full-length amino acid sequence of human Respl8 (SEQ

ID NO: 22) (the region encompassing the human Respl8 peptide [Human Peptide-pl] is highlighted in gray), and the nucleotide sequence encoding full-length human Respl8 (SEQ ID NO: 23) (the coding region is highlighted in gray).

[0066] Figure 17 provides the full-length amino acid sequence of mouse Respl8(SEQ ID

NO: 24) (the region encompassing the mouse Respl8 peptide [Mouse Peptide-pl] is highlighted in gray), and the nucleotide sequence encoding full-length mouse Respl8 (SEQ ID NO: 25) (the coding region is highlighted in gray).

[0067] Figure 18 shows a sequence alignment of Respl8 amino acid sequences from the indicated species. Amino acid sequences from mouse (SEQ ID NO: 24), rat (SEQ ID NO: 26), dog (SEQ ID NO: 27), gorilla (SEQ ID NO: 28), and human (SEQ ID NO: 22) comprising the Respl8 - related peptides are highlighted in gray. Residue positions that are fully conserved are indicated by (*), whereas residue positions that are semi-conserved are indicated by (.).

[0068] Figure 19, Panel a shows the effect of a single, bolus i.p. injection of mouse

Respl8 [Murine Peptide-pl] (10 mg/kg; gray squares) or Vehicle control (black squares) on basal (fasted) plasma glucose (FPG) concentration and oral glucose tolerance in high-fat fed mice. FPG concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Murine Peptide-pl or Vehicle control, and at minO glucose (lg/kg) in PBS was administered orally. Plasma glucose concentrations were determined at -30, 0, 15, 60 and 120 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide -pi and Vehicle-treated mice are indicated above the bars.)

[0069] Figure 19, Panel b shows the data from Figure 19, Panel a expressed as the percent change in plasma glucose concentration normalized to basal glucose concentration (min- 30) following a single, bolus i.p. injection of mouse Respl8 [Murine Peptide-pl] (10 mg/kg; gray squares) or Vehicle control (black squares) in high-fat fed mice, (n = 6 mice per group; p- values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[0070] Figure 19, Panel c shows the effect of a single, bolus i.p. injection of mouse

Respl8 [Murine Peptide-pl] (10 mg/kg; gray squares) and Vehicle control (black squares) on basal (fasted) plasma insulin concentration (FPI) and on glucose-stimulated insulin secretion (GSIS) in high-fat fed mice. FPI concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Murine Peptide-pl or Vehicle control, and at minO glucose (lg/kg) in PBS was administered orally. Plasma insulin concentrations were determined at -30, 0, 15, and 60 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[0071] Figure 19, Panel d shows the data from Figure 19, Panel c expressed as the percent change in plasma insulin concentration normalized to baseline (min-30) following a single, bolus i.p. injection of mouse Respl8 [Murine Peptide-pl] (10 mg/kg; gray squares) or Vehicle control (black squares) in high-fat fed mice, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-pl and Vehicle-treated mice are indicated below the bars.)

[0072] Figure 20 shows Tinag gene expression in EECs and ECs isolated from the indicated segments of the mouse gastrointestinal tract. Hatched bars represent expression in EECs, while solid bars represent expression in ECs.

[0073] Figure 21 provides the full-length amino acid sequence of human Tinag (SEQ ID

NO: 29) (the region encompassing the human Tinag -p3 and -p4 peptides [Human Peptide-p3 and Human Peptide -p4] is highlighted in gray), and the nucleotide sequence encoding full-length human Tinag (SEQ ID NO: 30) (the coding region is highlighted in gray). [0074] Figure 22 provides the full-length amino acid sequence of mouse Tinag (SEQ ID

NO: 31) (the region encompassing the mouse Tinag-p3 and -p4 peptides [Murine Peptide -p3 and Murine Peptide -p4] is highlighted in gray), and the nucleotide sequence encoding full-length mouse Tinag (SEQ ID NO: 32) (the coding region is highlighted in gray).

[0075] Figure 23 shows a sequence alignment of Tinag amino acid sequences from the indicated species. Amino acid sequences from chimpanzee (SEQ ID NO: 33), human (SEQ ID NO: 29), dog (SEQ ID NO: 34), mouse (SEQ ID NO: 31), and rat (SEQ ID NO: 35) comprising the Tiang - related peptides are highlighted in gray. Residue positions that are fully conserved are indicated by (*), whereas residue positions that are semi-conserved are indicated by (.).

[0076] Figure 24, Panel a shows the effect of a single, bolus i.p. injection of mouse

Tinag-p3 [Murine Peptide-p3] (10 mg/kg; gray squares) or Vehicle control (black squares) on basal (fasted) plasma glucose (FPG) concentration and oral glucose tolerance in high-fat fed mice. FPG concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Murine Peptide -p3 or Vehicle control, and at minO glucose (lg/kg) in PBS was administered orally. Plasma glucose concentrations were determined at -30, 0, 15, 60 and 120 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide -p3 and Vehicle-treated mice are indicated above the bars.)

[0077] Figure 24, Panel b shows the data from Figure 24, Panel a expressed as the percent change in plasma glucose concentration normalized to basal glucose concentration (min- 30) following a single, bolus i.p. injection of mouse Tinag-p3 [Murine Peptide -p3] (10 mg/kg; gray squares) or Vehicle control (black squares) in high-fat fed mice, (n = 6 mice per group; p- values determined by a student's t-test comparing Murine Peptide-p3 and Vehicle-treated mice are indicated above the bars.)

[0078] Figure 24, Panel c shows the effect of a single, bolus i.p. injection of mouse

Tinag -p3 [Murine Peptide-p3] (10 mg/kg; gray squares) and Vehicle control (black squares) on basal (fasted) plasma insulin concentration (FPI) and on glucose-stimulated insulin secretion (GSIS) in high-fat fed mice. FPI concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Murine Peptide -p3 or Vehicle control, and at minO glucose (lg/kg) in PBS was administered orally. Plasma insulin concentrations were determined at -30, 0, 15, and 60 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-p3 and Vehicle-treated mice are indicated above the bars.)

[0079] Figure 24, Panel d shows the data from Figure 24, Panel c expressed as the percent change in plasma insulin concentration normalized to baseline (min-30) following a single, bolus i.p. injection of Tinag-p3 [Murine Peptide-p3] (10 mg/kg; gray squares) or Vehicle control (black squares) in high-fat fed mice, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide -p3 and Vehicle-treated mice are indicated below the bars.)

[0080] Figure 25, Panel a shows the effect of a single, bolus i.p. injection of mouse

Tinag-p4 [Murine Peptide-p4] (10 mg/kg; gray squares) or Vehicle control (black squares) on basal (fasted) plasma glucose (FPG) concentration and oral glucose tolerance in high-fat fed mice. FPG concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Murine Peptide -4 or Vehicle control, and at minO glucose (lg/kg) in PBS was administered orally. Plasma glucose concentrations were determined at -30, 0, 15, 60 and 120 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide -4 and Vehicle -treated mice are indicated above the bars.)

[0081] Figure 25, Panel b shows the data from Figure 25, Panel a expressed as the percent change in plasma glucose concentration normalized to basal glucose concentration (min- 30) following a single, bolus i.p. injection of mouse Tinag-p4 [Murine Peptide -p4] (10 mg/kg; gray squares) or Vehicle control (black squares) in high-fat fed mice, (n = 6 mice per group; p- values determined by a student's t-test comparing Murine Peptide-p4 and Vehicle-treated mice are indicated above the bars.)

[0082] Figure 25, Panel c shows the effect of a single, bolus i.p. injection of mouse

Tinag-p4 [Murine Peptide-p4] (10 mg/kg; gray squares) and Vehicle control (black squares) on basal (fasted) plasma insulin concentration (FPI) and on glucose-stimulated insulin secretion (GSIS) in high-fat fed mice. FPI concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Murine Peptide -p4 or Vehicle control, and at minO glucose (lg/kg) in PBS was administered orally. Plasma insulin concentrations were determined at -30, 0, 15, and 60 minutes, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide-p4 and Vehicle-treated mice are indicated above the bars.)

[0083] Figure 25, Panel d shows the data from Figure 25, Panel c expressed as the percent change in plasma insulin concentration normalized to baseline (min-30) following a single, bolus i.p. injection of Tinag-p4 [Murine Peptide-p4] (10 mg/kg; gray squares) or Vehicle control (black squares) in high-fat fed mice, (n = 6 mice per group; p-values determined by a student's t-test comparing Murine Peptide -p4 and Vehicle-treated mice are indicated below the bars.)

DETAILED DESCRIPTION

[0084] Before the present invention is further described, it is to be understood that the invention is not limited to the particular embodiments set forth herein, and it is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting.

[0085] Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limit of that range and any other stated or intervening value in that stated range, is encompassed within the invention. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges, and are also encompassed within the invention, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the invention. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.

[0086] It must be noted that as used herein and in the appended claims, the singular forms "a," "an," and "the" include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to "the Human Ednl Peptide" includes reference to one or more Human Ednl Peptides, and so forth. It is further noted that the claims may be drafted to exclude any optional element. As such, this statement is intended to serve as antecedent basis for use of such exclusive terminology such as "solely," "only" and the like in connection with the recitation of claim elements, or use of a "negative" limitation. [0087] The publications discussed herein are provided solely for their disclosure prior to the filing date of the present application. Nothing herein is to be construed as an admission that the present invention is not entitled to antedate such publication by virtue of prior invention. Further, the dates of publication provided may be different from the actual publication dates which may need to be independently confirmed.

Overview

[0088] The present disclosure contemplates the use of the Modulators described herein, and compositions thereof, to treat and/or prevent various diseases, disorders and conditions, and/or the symptoms thereof. In some embodiments, the diseases, disorders and conditions, and/or the symptoms thereof, pertain to metabolic-related disorders, while in other embodiments they pertain to glucose metabolism disorders. By way of example, but not limitation, the Modulators, and compositions thereof, can be used for the treatment and/or prevention of diabetes (e.g., Type 2 diabetes), insulin resistance and diseases, disorders and conditions characterized by insulin resistance, decreased insulin production, hyperglycemia,

hypoinsulinemia, and metabolic syndrome. The Modulators, and compositions thereof, may also be useful in, for example, subjects who may be overweight or obese.

[0089] "Ednl ," or "endothelin- 1 ," encompasses peptides and variants thereof that are encoded by the Ednl gene or homologs thereof. Ednl is found in many mammals, including humans, non-human primates, rodents (e.g., mice) and canines.

[0090] Peptide subsequences predicted to be derived from the Ednl gene product are described herein. For example, human and murine peptides that are subsequences of full-length human Ednl or mouse Ednl have been identified (see highlighted sequences in Figures 2 and 3A). While an understanding of all of the characteristics of these murine peptides and human peptides is not required in order to practice embodiments of the present disclosure, they are believed to be secreted peptides.

[0091] "Habp2," or "hyaluronan binding protein 2" (also known as "factor VII activating protein"; "hyaluronic acid binding protein 2"; "plasma hyaluronan binding protein"; and

"hepatocyte growth factor activator-like protein") encompasses peptides and variants thereof that are encoded by the Habp2 gene or homologs thereof. Habp2 is found in many mammals, including humans, non-human primates, rodents (e.g., mice), and canines. [0092] Peptide subsequences predicted to be derived from the Habp2 gene product are described herein. For example, human and murine peptides that are subsequences of full-length human Habp2 or mouse Habp2 have been identified (see highlighted sequences in Figures 7A and 8A). While an understanding of all of the characteristics of these murine peptides and human peptides is not required in order to practice embodiments of the present disclosure, they are believed to be secreted peptides.

[0093] "Kazaldl," or "kazal-type serine peptidase inhibitor domain" (also known as

"BONOl"; "IGFBP-related protein 10"; "bone- and odontoblast-expressed gene 1"; "FKSG28"; and "FKSG40") encompasses peptides and variants thereof that are encoded by the Kazaldl gene or homologs thereof. Kazaldl is found in many mammals, including humans, non-human primates, rodents (e.g., mice), and canines.

[0094] Peptide subsequences predicted to be derived from the Kazaldl gene product are described herein. For example, human and murine peptides that are subsequences of full-length human Kazaldl or mouse Kazaldl have been identified (see highlighted sequences in Figures 12A and 13 A). While an understanding of all of the characteristics of these murine peptides and human peptides is not required in order to practice embodiments of the present disclosure, they are believed to be secreted peptides.

[0095] "Respl8," or "regulated endocrine-specific protein 18" encompasses peptides and variants thereof that are encoded by the Respl8 gene or homologs thereof. Respl8 is found in many mammals, including humans, non-human primates, rodents (e.g., mice), and canines.

[0096] Peptide subsequences predicted to be derived from the Respl8 gene product are described herein. For example, human and murine peptides that are subsequences of full-length human Respl8 or mouse Respl8 have been identified (see highlighted sequences in Figures 16 and 17). While an understanding of all of the characteristics of these murine peptides and human peptides is not required in order to practice embodiments of the present disclosure, they are believed to be secreted peptides.

[0097] "Tinag," or "tubulointerstitial nephritis antigen" encompasses peptides and variants thereof that are encoded by the Tinag gene or homologs thereof. Tinag is found in many mammals, including humans, non-human primates, rodents (e.g., mice), and canines.

[0098] Peptide subsequences predicted to be derived from the Tinag gene product are described herein. For example, human and murine peptides that are subsequences of full-length human Tinag or mouse Tinag have been identified (see highlighted sequences in Figures 21 and 22). While an understanding of all of the characteristics of these murine peptides and human peptides is not required in order to practice embodiments of the present disclosure, they are believed to be secreted peptides.

Definitions

[0099] The terms "patient" or "subject" are used interchangeably to refer to a human or a non-human animal (e.g., a mammal).

[00100] The terms 'treat", "treating", treatment" and the like refer to a course of action

(such as administering a Modulator or a pharmaceutical composition comprising a Modulator) initiated after a disease, disorder or condition, or a symptom thereof, has been diagnosed, observed, and the like so as to eliminate, reduce, suppress, mitigate, or ameliorate, either temporarily or permanently, at least one of the underlying causes of a disease, disorder, condition afflicting a subject, or at least one of the symptoms associated with a disease, disorder, condition afflicting a subject. Thus, treatment includes inhibiting (i.e., arresting the development or further development of the disease, disorder or condition or clinical symptoms association therewith) an active disease (e.g., so as to decrease the level of insulin and/or glucose in the bloodstream, to increase glucose tolerance so as to minimize fluctuation of glucose levels, and/or so as to protect against diseases caused by disruption of glucose homeostasis).

[00101] The term "in need of treatment" as used herein refers to a judgment made by a physician or other caregiver that a subject requires or will benefit from treatment. This judgment is made based on a variety of factors that are in the realm of the physician's or caregiver's expertise.

[00102] The terms "prevent", "preventing", "prevention" and the like refer to a course of action (such as administering a Modulator or a pharmaceutical composition comprising a Modulator) initiated in a manner (e.g., prior to the onset of a disease, disorder, condition or symptom thereof) so as to prevent, suppress, inhibit or reduce, either temporarily or permanently, a subject's risk of developing a disease, disorder, condition or the like (as determined by, for example, the absence of clinical symptoms) or delaying the onset thereof, generally in the context of a subject predisposed to having a particular disease, disorder or condition. In certain instances, the terms also refer to slowing the progression of the disease, disorder or condition or inhibiting progression thereof to a harmful or otherwise undesired state.

[00103] The term "in need of prevention" as used herein refers to a judgment made by a physician or other caregiver that a subject requires or will benefit from preventative care. This judgment is made based on a variety of factors that are in the realm of a physician's or caregiver's expertise.

[00104] The phrase "therapeutically effective amount" refers to the administration of an agent to a subject, either alone or as a part of a pharmaceutical composition and either in a single dose or as part of a series of doses, in an amount that is capable of having any detectable, positive effect on any symptom, aspect, or characteristics of a disease, disorder or condition when administered to a patient. The therapeutically effective amount can be ascertained by measuring relevant physiological effects. For example, in the case of a hyperglycemic condition, a lowering or reduction of blood glucose or an improvement in glucose tolerance test can be used to determine whether the amount of an agent is effective to treat the hyperglycemic condition. For example, a therapeutically effective amount is an amount sufficient to reduce or decrease any level (e.g., a baseline level) of FPG, wherein, for example, the amount is sufficient to reduce a FPG level greater than 200 mg/dl to less than 200 mg/dl, wherein the amount is sufficient to reduce a FPG level between 175 mg/dl and 200 mg/dl to less than the starting level, wherein the amount is sufficient to reduce a FPG level between 150 mg/dl and 175 mg/dl to less than the starting level, wherein the amount is sufficient to reduce a FPG level between 125 mg/dl and 150 mg/dl to less than the starting level, and so on (e.g., reducing FPG levels to less than 125 mg/dl, to less than 120 mg/dl, to less than 115 mg/dl, to less than 110 mg/dl, etc.). In the case of HbAIc levels, the effective amount is an amount sufficient to reduce or decrease levels by more than about 10% to 9%, by more than about 9% to 8%, by more than about 8% to 7%, by more than about 7% to 6%, by more than about 6% to 5%, and so on. More particularly, a reduction or decrease of HbAIc levels by about 0.1%, 0.25%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1%, 1.5%, 2%, 3%, 4%, 5%, 10%, 20%, 30%, 33%, 35%, 40%, 45%, 50%, or more is contemplated by the present disclosure. The therapeutically effective amount can be adjusted in connection with dosing regimen and diagnostic analysis of the subject's condition and the like.

[00105] The phrase "in a sufficient amount to effect a change" means that there is a detectable difference between a level of an indicator measured before (e.g., a baseline level) and after administration of a particular therapy. Indicators include any objective parameter (e.g., level of glucose or insulin) or subjective parameter (e.g., subject's feeling of well-being).

[00106] The phrase "glucose tolerance", as used herein, refers to the ability of a subject to control the level of plasma glucose and/or plasma insulin when glucose intake fluctuates. For example, glucose tolerance encompasses the subject's ability to reduce, within about 120 minutes, the level of plasma glucose back to a level determined before the intake of glucose.

[00107] Broadly speaking, the terms "diabetes" and "diabetic" refer to a progressive disease of carbohydrate metabolism involving inadequate production or utilization of insulin, frequently characterized by hyperglycemia and glycosuria. The terms "pre-diabetes" and "pre- diabetic" refer to a state wherein a subject does not have the characteristics, symptoms and the like typically observed in diabetes, but does have characteristics, symptoms and the like that, if left untreated, may progress to diabetes. The presence of these conditions may be determined using, for example, either the fasting plasma glucose test (FPG) or the oral glucose tolerance test (OGTT). Both require a subject to fast for at least 8 hours prior to initiating the test. In the FPG test, a subject's blood glucose is measured after the conclusion of the fasting; generally, the subject fasts overnight and the blood glucose is measured in the morning before the subject eats. A healthy subject would generally have a FPG concentration between 90 and about 100 mg/dl, a subject with "pre-diabetes" would generally have a FPG concentration between about 100 and about 125 mg/dl, and a subject with "diabetes" would generally have a FPG level above about 126 mg/dl. In the OGTT, a subject's blood glucose is measured after fasting and again two hours after drinking a glucose-rich beverage. Two hours after consumption of the glucose-rich beverage, a healthy subject generally has a blood glucose concentration below about 140 mg/dl, a pre-diabetic subject generally has a blood glucose concentration about 140 to about 199 mg/dl, and a diabetic subject generally has a blood glucose concentration about 200 mg/dl or above. While the aforementioned glycemic values pertain to human subjects, normoglycemia, moderate hyperglycemia and overt hyperglycemia are scaled differently in murine subjects. A healthy murine subject after a four-hour fast would generally have a FBG concentration between 100 to 150mg/dl, a murine subject with "pre-diabetes" would generally have a FPG concentration between 175 to 250 mg/dl and a murine subject with "diabetes" would generally have a FPG concentration between 250 to >600mg/dl. [00108] The term "insulin resistance" as used herein refers to a condition where a normal amount of insulin is unable to produce a normal physiological or molecular response. In some cases, a hyper-physiological amount of insulin, either endogenously produced or exogenously administered, is able to overcome the insulin resistance in whole or in part and produce a biologic response.

[00109] The term "metabolic syndrome" refers to an associated cluster of traits that includes, but is not limited to, hyperinsulinemia, abnormal glucose tolerance, obesity, redistribution of fat to the abdominal or upper body compartment, hypertension, dysfibrinolysis, and dyslipidemia characterized by high triglycerides, low HDL-cholesterol, and small dense LDL particles. Subjects having metabolic syndrome are at risk for development of Type 2 diabetes and, for example, atherosclerosis.

[00110] The phrase "glucose metabolism disorder" encompasses any disorder

characterized by a clinical symptom or a combination of clinical symptoms that is associated with an elevated level of glucose and/or an elevated level of insulin in a subject relative to a healthy individual. Elevated levels of glucose and/or insulin may be manifested in the following diseases, disorders and conditions: hyperglycemia, type II diabetes (e.g., insulin-resistance diabetes), gestational diabetes, type I diabetes, insulin resistance, impaired glucose tolerance, hyperinsulinemia, impaired glucose metabolism, pre-diabetes, metabolic disorders (such as metabolic syndrome which is also referred to as syndrome X), hypoglycemia, and obesity, among others. The Modulators of the present disclosure, and compositions thereof, can be used to, for example, achieve and/or maintain glucose homeostasis, e.g., to reduce glucose level in the bloodstream and/or to reduce insulin level to a range found in a healthy subject.

[00111] The term "hyperglycemia", as used herein, refers to a condition in which an elevated amount of glucose circulates in the blood plasma of a subject relative to a healthy individual. Hyperglycemia can be diagnosed using methods known in the art, including measurement of fasting blood glucose levels as described herein.

[00112] The term "hyperinsulinemia", as used herein, refers to a condition in which there are elevated levels of circulating insulin when, concomitantly, blood glucose levels are either elevated or normal. Hyperinsulinemia can be caused by insulin resistance which is associated with dyslipidemia such as high triglycerides, high cholesterol, high low-density lipoprotein (LDL) and low high-density lipoprotein (HDL); high uric acids levels; polycystic ovary syndrome; type II diabetes and obesity. Hyperinsulinemia can be diagnosed as having a plasma insulin level higher than about 2 μΙΙ/mL.

[00113] The term "Inhibitors" refers to agents that, for example, partially or totally block stimulation, decrease, prevent, delay activation, inactivate, desensitize, or down-regulate the function or activity of one or more Peptides, such as, for example, antagonists including antibodies, small molecule antagonist compounds, and antagonistic peptides distinguishable from the peptides disclosed herein; other examples of Inhibitors are described below.

[00114] The term "Activators" refers to agents that, for example, stimulate, increase, activate, facilitate, enhance activation, sensitize or up-regulate the function or activity of one or more Peptides, such as, for example, agonists including antibodies, small molecule agonists, the peptides disclosed herein, and other agonistic peptides distinguishable from the peptides disclosed herein; other examples of Activators are described below.

[00115] The term "Modulators" collectively refers to Inhibitors and Activators.

[00116] The terms "modulate", "modulation" and the like refer to the ability of the

Inhibitors and the Activators to decrease or increase, respectively, the function or activity of one or more Peptides (or the nucleic acid molecules encoding them), either directly or indirectly. Modulation may occur in vitro or in vivo.

[00117] As used herein, "homologues" or "variants" are used interchangeably to refer to amino acid or DNA sequences that are similar to reference amino acid or nucleic acid sequences, respectively. For example, homologues may refer to nucleic acid or amino acid sequences in one species that are similar to nucleic acid or amino acid sequences in another species. Alternatively, homologues may refer to nucleic acid or amino acid sequences in one species that are similar to nucleic acid or amino acid sequences in the same species. Homologues or variants encompass naturally occurring DNA sequences and proteins encoded thereby and their isoforms. The homologues also include known allelic or splice variants of a protein or gene. Homologues and variants also encompass nucleic acid sequences that vary in one or more bases from a naturally- occurring DNA sequence but still translate into an amino acid sequence that corresponds to the naturally-occurring protein due to degeneracy of the genetic code. Homologues and variants may also refer to those that differ from the naturally-occurring sequences by one or more conservative substitutions and/or tags and/or conjugates. [00118] The terms "polypeptide," "peptide," and "protein", used interchangeably herein, refer to a polymeric form of amino acids of any length, which can include genetically coded and non-genetically coded amino acids, chemically or biochemically modified or derivatized amino acids, and polypeptides having modified peptide backbones. The terms include fusion proteins, including, but not limited to, fusion proteins with a heterologous amino acid sequence, fusion proteins with heterologous and homologous leader sequences, with or without N-terminal methionine residues; immunologically tagged proteins; and the like. While the aforementioned terms can be used interchangeably, in general the term "peptide" refers to a polymeric form of amino acids of less than about 50 amino acids in length.

[00119] It will be appreciated that throughout this present disclosure reference is made to amino acids according to the single letter or three letter codes. For the reader's convenience, the single and three letter amino acid codes are provided below:

G Glycine Gly P Proline Pro

A Alanine Ala V Valine Val

L Leucine Leu I Isoleucine He

M Methionine Met C Cysteine Cys

F Phenylalanine Phe Y Tyrosine Tyr

W Tryptophan Trp H Histidine His

K Lysine Lys R Arginine Arg

Q Glutamine Gin N Asparagine Asn

E Glutamic Acid Glu D Aspartic Acid Asp

S Serine Ser T Threonine Thr

[00120] The terms "DNA", "nucleic acid", "nucleic acid molecule", "polynucleotide" and the like are used interchangeably herein to refer to a polymeric form of nucleotides of any length, either deoxyribonucleotides or ribonucleotides, or analogs thereof. Non-limiting examples of polynucleotides include linear and circular nucleic acids, messenger RNA (mRNA),

complementary DNA (cDNA), recombinant polynucleotides, vectors, probes, primers and the like. [00121] The term "Probe" refers to a fragment of DNA or R A corresponding to a gene or sequence of interest, wherein the fragment has been labeled radioactively (e.g., by

incorporating 32 ^p or 35 ^s ) or with some other detectable molecule, such as biotin, digoxygenin or fluorescein. As stretches of DNA or RNA with complementary sequences will hybridize, a probe can be used to, for example, label viral plaques, bacterial colonies or bands on a gel that contain the gene of interest. A probe can be cloned DNA or it can be a synthetic DNA strand; the latter can be used to obtain a cDNA or genomic clone from an isolated a protein by, for example, microsequencing a portion of the protein, deducing the nucleic acid sequence encoding the protein, synthesizing an oligonucleotide carrying that sequence, radiolabeling the sequence and using it as a probe to screen a cDNA library or a genomic library.

[00122] The term "heterologous" refers to two components that are defined by structures derived from different sources. For example, in the context of a polypeptide, a "heterologous" polypeptide may include operably linked amino acid sequences that are derived from different polypeptides (e.g., a first component comprising a recombinant peptide and a second component derived from a native peptide). Similarly, in the context of a polynucleotide encoding a chimeric polypeptide, a "heterologous" polynucleotide may include in operably linked nucleic acid sequences that can be derived from different genes (e.g., a first component from a nucleic acid encoding a peptide according to an embodiment disclosed herein and a second component from a nucleic acid encoding a carrier polypeptide). Other exemplary "heterologous" nucleic acids include expression constructs in which a nucleic acid comprising a coding sequence is operably linked to a regulatory element (e.g., a promoter) that is from a genetic origin different from that of the coding sequence (e.g., to provide for expression in a host cell of interest, which may be of different genetic origin than the promoter, the coding sequence or both). For example, a T7 promoter operably linked to a polynucleotide encoding an Ednl polypeptide or domain thereof is said to be a heterologous nucleic acid. In the context of recombinant cells, "heterologous" can refer to the presence of a nucleic acid (or gene product, such as a polypeptide) that is of a different genetic origin than the host cell in which it is present.

[00123] The term "operably linked" refers to linkage between molecules to provide a desired function. For example, "operably linked" in the context of nucleic acids refers to a functional linkage between a nucleic acid expression control sequence (such as a promoter, signal sequence, or array of transcription factor binding sites) and a second polynucleotide, wherein the expression control sequence affects transcription and/or translation of the second polynucleotide. In the context of a polypeptide, "operably linked" refers to a functional linkage between amino acid sequences (e.g., of different domains) to provide for a described activity of the polypeptide.

[00124] As used herein in the context of the structure of a polypeptide, "N-terminus" (or

"amino terminus") and "C-terminus" (or "carboxyl terminus") refer to the extreme amino and carboxyl ends of the polypeptide, respectively, while the terms "N-terminal" and "C-terminal" refer to relative positions in the amino acid sequence of the polypeptide toward the N-terminus and the C-terminus, respectively, and can include the residues at the N-terminus and C-terminus, respectively. "Immediately N-terminal" or "immediately C-terminal" refers to a position of a first amino acid residue relative to a second amino acid residue where the first and second amino acid residues are covalently bound to provide a contiguous amino acid sequence.

[00125] "Derived from", in the context of an amino acid sequence or polynucleotide sequence (e.g., an amino acid sequence "derived from" a Kazaldl polypeptide), is meant to indicate that the polypeptide or nucleic acid has a sequence that is based on that of a reference polypeptide or nucleic acid (e.g., a naturally occurring Kazaldl polypeptide or a Kazaldl - encoding nucleic acid), and is not meant to be limiting as to the source or method in which the protein or nucleic acid is made. By way of example, the term "derived from" includes homologues or variants of reference amino acid or DNA sequences.

[00126] "Isolated" refers to a peptide of interest that, if naturally occurring, is in an environment different from that in which it may naturally occur. "Isolated" is meant to include peptides that are within samples that are substantially enriched for the peptide of interest and/or in which the peptide of interest is partially or substantially purified. Where the peptide is not naturally occurring, "isolated" indicates the peptide has been separated from an environment in which it was made by either synthetic or recombinant means.

[00127] "Enriched" means that a sample is non-naturally manipulated (e.g., by a scientist or a clinician) so that a peptide of interest is present in a) a greater concentration (e.g., at least 3- fold greater, at least 4-fold greater, at least 8-fold greater, at least 64-fold greater, or more) than the concentration of the peptide in the starting sample, such as a biological sample (e.g., a sample in which the peptide naturally occurs or in which it is present after administration), or b) a greater concentration than the environment in which the peptide was made (e.g., as in a bacterial cell).

[00128] "Substantially pure" indicates that a component (e.g., a polypeptide) makes up greater than about 50% of the total content of the composition and typically, greater than about 60% of the total polypeptide content. More typically, "substantially pure" refers to compositions in which at least 75%, at least 85%, at least 90% or more of the total composition is the component of interest. In some cases, the polypeptide will make up greater than about 90%, or greater than about 95% of the total content of the composition.

[00129] The terms "antibodies" (Abs) and "immunoglobulins" (Igs) refer to glycoproteins having the same structural characteristics. While antibodies exhibit binding specificity to a specific antigen, immunoglobulins include both antibodies and other antibody-like molecules which lack antigen specificity. Antibodies are described in detail hereafter.

[00130] The term "monoclonal antibody" refers to an antibody obtained from a population of substantially homogeneous antibodies, that is, the individual antibodies comprising the population are identical except for possible naturally occurring mutations that may be present in minor amounts. Monoclonal antibodies are highly specific, being directed against a single antigenic site. In contrast to polyclonal antibody preparations which include different antibodies directed against different determinants (epitopes), each monoclonal antibody is directed against a single determinant on the antigen.

[00131] An "isolated" antibody is one which has been separated and/or recovered from contaminant components of its natural environment; such contaminant components are materials which might interfere with diagnostic or therapeutic uses for the antibody, and may include enzymes, hormones, and other proteinaceous or nonproteinaceous solutes.

PEPTIDES AND NUCLEIC ACIDS ENCODING SAME

Ednl

[00132] "Ednl ," or "endothelin- 1 ," encompasses peptides and variants thereof that are encoded by the Ednl gene or homologs thereof. Ednl is found in many mammals, including humans, non-human primates, rodents (e.g., mice) and canines. "Ednl" encompasses human and murine peptides and variants thereof that are encoded by the Ednl gene or homologs thereof. [00133] As depicted in Figure 1, Ednl gene expression is prevalent in certain enteroendocrine cells (EECs) of the gastrointestinal tract (e.g., EECs from the colon). Figure 4 depicts a sequence alignment of Ednl amino acid sequences from the indicated species, including a subsequence of Ednl amino acid sequences.

A. Ednl Peptide-related Amino Acid and Nucleic Acid Sequences

[00134] Mouse and human Ednl peptides have been identified, which peptides are Ednl gene products (Figure 4).

[00135] Non-limiting examples of Ednl peptides are provided below.

CWNFCQA-COOH (SEQ ID NO: 56); and

CWTFCQA-COOH (SEQ ID NO: 57).

[00136] Figure 5 indicates the effect of a mouse Ednl [Murine Peptide-pl : CWNFCQA

(SEQ ID NO: 56)] on elevating blood glucose levels and reducing glucose-stimulated insulin secretion. These data were generated as described in the Experimental section. Because they have the same amino acid sequence, the activity of human Ednl [Human Peptide-pl] is predicted to be comparable to that of the corresponding mouse Ednl [Murine Peptide-pl].

[00137] While a precise understanding of the Ednl Peptides' mechanism of action is not required in order to practice the embodiments of the present disclosure, the increase in systemic glycemia associated with the Edbl Peptides is believed to be dependent on reduced insulin concentration. This increase in systemic glycemia is thought to be attributed to one or more physiological responses, including reduced insulin production and/or secretion by pancreatic beta-cells; reduced insulin production and/or secretion due to a secondary messenger (e.g., glucagon or somatostatin); and increased insulin clearance by peripheral tissues, such as the liver.

[00138] As indicated in Figure 5, Ednl Murine Peptide-pl increases glucose levels and reduces glucose-stimulated insulin secretion. The Ednl Murine Peptide-pl increases circulating glucose concentration (Figure 5, Panel a), and decreases circulating insulin concentration (Figure 5, Panel c).

[00139] As used herein, the term "Ednl" refers to Ednl Peptides of the present disclosure, or fragments thereof, or Ednl Nucleic Acid Molecules of the present disclosure, which include their naturally-occurring and non-naturally occurring isoforms, allelic variants and splice variants. As previously noted, a Peptide also refers to peptides that have one or more alterations in the amino acid residues (e.g., at locations that are not conserved across variants or species) while retaining the conserved domains and having the same biological activity as the naturally- occurring Peptides. "Ednl" also encompasses nucleic acid sequences that vary in one or more bases from a naturally-occurring DNA sequence but still translate into an amino acid sequence that corresponds to a Peptide due to degeneracy of the genetic code. For example, Ednl may refer to amino acid sequences that differ from the naturally-occurring sequences (e.g., Ednl Peptides) by one or more conservative substitutions, tags, or conjugates.

[00140] Thus, in addition to any naturally-occurring Ednl polypeptide (e.g., an Ednl

Peptide), the present disclosure contemplates having 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 usually no more than 20, 10, or 5 amino acid substitutions, where the substitution is usually a conservative amino acid substitution.

[00141] By "conservative amino acid substitution" generally refers to substitution of amino acid residues within the following groups: 1) L, I, M, V, F; 2) R, K; 3) F, Y, H, W, R; 4) G, A, T, S; 5) Q, N; and 6) D, E. Conservative amino acid substitutions preserve the activity of the protein by replacing an amino acid(s) in the protein with an amino acid with a side chain of similar acidity, basicity, charge, polarity, or size of the side chain. Guidance for substitutions, insertions, or deletions may be based on alignments of amino acid sequences of different variant proteins or proteins from different species. For example, according to the alignments shown in Figure 4, at certain residue positions that are fully conserved (*), substitutions, deletions or insertions may not be allowed, while at other positions where one or more residues are not conserved, an amino acid change can be tolerated. Residues that are semi-conserved (.) may tolerate changes that preserve charge, polarity, and/or size.

[00142] Ednl Peptides are active fragments containing contiguous amino acid residues derived from the full-length Ednl polypeptide. In Figure 4, the regions encompassing the human peptides and the murine peptides are highlighted in gray.

[00143] The length of contiguous amino acid residues of a peptide or a polypeptide subsequence varies depending on the specific naturally-occurring amino acid sequence from which the subsequence is derived. In general, peptides and polypeptides may be from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 40 amino acids, from about 40 amino acids to about 50 amino acids, from about 50 amino acids to about 75 amino acids, from about 75 amino acids to about 100 amino acids, from about 100 amino acids to about 150 amino acids, from about 150 amino acids to about 200 amino acids, or from about 200 amino acids up to the full-length peptide or polypeptide. Peptides have a length that is less than the full length of the naturally-occurring polypeptide.

[00144] In some embodiments, the Ednl Peptides can have a length of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 35 amino acids, from about 40 amino acids to about 45 amino acids, from about 45 amino acids to about 50 amino acids, or from more than about 50 amino acids. In certain embodiments, the peptides contemplated by the present disclosure are less than about 35 amino acids in length (see Figure 4).

[00145] Additionally, the Ednl Peptides can have a defined sequence identity compared to a reference sequence over a defined length of contiguous amino acids (e.g., a "comparison window"). Methods of alignment of sequences for comparison are well-known in the art.

Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482 (1981), by the homology alignment algorithm of Needleman & Wunsch, J. Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson & Lipman, Proc. Nat'l. Acad. Sci. USA 85:2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by manual alignment and visual inspection (see, e.g., Current Protocols in Molecular Biology (Ausubel et al, eds. 1995 supplement)).

[00146] As an example, a suitable Peptide can comprise an amino acid sequence having at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 98%, or at least about 99%, amino acid sequence identity to a contiguous stretch of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 12 amino acids, from about 12 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 22 amino acids, from about 22 amino acids to about 25 amino acids, from about 25 amino acids to about 27 amino acids, from about 27 amino acids to about 29 amino acids, or from more than about 29 amino acids of one of the following reference amino acid sequences:

CWNFCQA-COOH (SEQ ID NO: 56); or

CWTFCQA-COOH (SEQ ID NO: 57).

[00147] For example, in some embodiments, a suitable Ednl Peptide can comprise an amino acid sequence having at least about 75%, at least about 80%, at least about 85%, at least about 90%), at least about 95%, at least about 98%, or at least about 99%, amino acid sequence identity to the following sequence: CWXFCQA (SEQ ID NO: 36), where X is a semi-conserved residue (e.g., where X is N or T), and where the peptide has a length of from about 5 amino acids to about 50 amino acids, or more than 50 amino acids. For example, the Ednl Peptide can have a length of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 12 amino acids, from about 12 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 22 amino acids, from about 22 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 35 amino acids, from about 35 amino acids to about 40 amino acids, from about 40 amino acids to about 45 amino acids, from about 45 amino acids to about 50 amino acids, or from more than about 50 amino acids. In some cases, the carboxyl terminal amino acid can be amidated.

[00148] The Ednl Peptides may be isolated from a natural source (e.g., in an environment other than its naturally-occurring environment) and also may be recombinantly made (e.g., in a genetically modified host cell such as bacteria; yeast; Pichia; insect cells; and the like), where the genetically modified host cell is modified with a nucleic acid comprising a nucleotide sequence encoding the peptide. The Ednl Peptides may also be synthetically produced (e.g., by cell-free chemical synthesis). Methods of productions are described in more detail below.

[00149] An Ednl Peptide may be generated using recombinant techniques to manipulate different Ednl- related nucleic acids known in the art to provide constructs capable of encoding the Peptide. It will be appreciated that, when provided a particular amino acid sequence, the ordinary skilled artisan will recognize a variety of different nucleic acid molecules encoding such amino acid sequence in view of her background and experience in, for example, molecular biology.

[00150] Ednl- related nucleic acid sequences and amino acid sequences are known and available in the art and include the following (listed with their corresponding GenBank accession nos).: 1) Homo sapiens: amino acid sequence: NP 001946; nucleotide sequence: NM 001955; amino acid sequence: NP 001 161791 ; nucleotide sequence: NM 001 168319; 2) Rattus norvegicus: amino acid sequence: NP 036680; nucleotide sequence: NM_012548; 3) Canis lupus familiaris: amino acid sequence: NP 001002956; nucleotide sequence: NM 001002956;

4) Pan troglodytes : amino acid sequence: XP_518241 ; nucleotide sequence: XM_518241 ; and

5) Mus musculus: amino acid sequence: NP_034234; nucleotide sequence: NM_010104.

Exemplary amino acid sequences are depicted in Figures 2, 3A, 3B, and 4.

Habp2

[00151] "Habp2," or "hyaluronan binding protein 2" (also known as "factor VII activating protein"; "hyaluronic acid binding protein 2"; "plasma hyaluronan binding protein"; and

"hepatocyte growth factor activator-like protein") encompasses peptides and variants thereof that are encoded by the Habp2 gene or homologs thereof. Habp2 is found in many mammals, including humans, non-human primates, rodents (e.g., mice), and canines.

[00152] As depicted in Figure 6, Habp2 gene expression is prevalent in certain EECs of the gastrointestinal tract (e.g., EECs of the duodenum). Figure 9 depicts a sequence alignment of Habp2 amino acid sequences from the indicated species, including a subsequence of Habp2 amino acid sequences.

B. Habp2 Peptide -related Amino Acid and Nucleic Acid Sequences

[00153] Mouse and human Habp2 peptides have been identified, which peptides are

Habp2 gene products (Figure 9). In some cases, an Habp2 Peptide comprises the following sequence: PGVYTQVXiKFLNWIKX ₂ TX ₃ X4X ₅ X6 7 8 (SEQ ID NO: 37), where each of X Xg are semi-conserved residues, which residues in some embodiments are as follows: Xi and X ₂ are A or T; X ₃ is I or M; X ₄ is K, Q, or H; X ₅ is S, K, or R; X ₆ is E or G; X? is S or A; X ₈ is S or G; and X is F or L.

[00154] Non-limiting examples of Habp2 peptides are provided below. PGVYTQVTKFLNWIKATIKSESGF (SEQ ID NO: 58);

PGVYTQVAKFLNWIKATIQKGSSF (SEQ ID NO: 59);

PGVYTQVTKFLNWIKTTMHREAGL (SEQ ID NO: 60); and

PGVYTQVTKFLNWIKTTMHKEAGL (SEQ ID NO: 61).

[00155] Figure 10 indicates the effect of a mouse Habp2 [Murine Peptide - i :

PGVYTQVTKFLNWIKTTMHREAGL (SEQ ID NO: 60)] on elevating blood glucose levels and reducing glucose-stimulated insulin secretion. These data were generated as described in the Experimental section. The activity of human Habp2 [Human Peptide-pl] is predicted to be comparable to that of the corresponding mouse Habp2 [Murine Peptide-pl] in view of the conservative and semi-conservative nature of the amino acid substitutions.

[00156] While a precise understanding of the Habp2 Peptides' mechanism of action is not required in order to practice the embodiments of the present disclosure, the increase in systemic glycemia associated with the Habp2 Peptides is believed to be dependent on reduced insulin concentration. This increase in systemic glycemia is thought to be attributed to one or more physiological responses, including reduced insulin production and/or secretion by pancreatic beta-cells; reduced insulin production and/or secretion due to a secondary messenger (e.g., glucagon or somatostatin); and increased insulin clearance by peripheral tissues, such as the liver.

[00157] As indicated in Figure 10, Habp2 Peptide increases glucose levels and reduces glucose-stimulated insulin secretion. The Habp2 Peptide increases circulating glucose concentration, and decreases circulating insulin concentration.

[00158] As used herein, the term "Habp2" refers to Habp2 Peptides of the present disclosure, or fragments thereof, or Habp2 Nucleic Acid Molecules of the present disclosure, which include their naturally-occurring and non-naturally occurring isoforms, allelic variants and splice variants. As previously noted, a Habp2 Peptide also refers to peptides that have one or more alterations in the amino acid residues (e.g., at locations that are not conserved across variants or species) while retaining the conserved domains and having the same biological activity as the naturally-occurring Peptides. "Habp2" also encompasses nucleic acid sequences that vary in one or more bases from a naturally-occurring DNA sequence but still translate into an amino acid sequence that corresponds to a Peptide due to degeneracy of the genetic code. For example, Habp2 may refer to amino acid sequences that differ from the naturally-occurring sequences (e.g., Habp2 Peptides) by one or more conservative substitutions, tags, or conjugates.

[00159] Thus, in addition to any naturally-occurring Habp2 polypeptide (e.g., a Habp2

Peptide), the present disclosure contemplates having 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 usually no more than 20, 10, or 5 amino acid substitutions, where the substitution is usually a conservative amino acid substitution.

[00160] By "conservative amino acid substitution" generally refers to substitution of amino acid residues within the following groups: 1) L, I, M, V, F; 2) R, K; 3) F, Y, H, W, R; 4) G, A, T, S; 5) Q, N; and 6) D, E. Conservative amino acid substitutions preserve the activity of the protein by replacing an amino acid(s) in the protein with an amino acid with a side chain of similar acidity, basicity, charge, polarity, or size of the side chain. Guidance for substitutions, insertions, or deletions may be based on alignments of amino acid sequences of different variant proteins or proteins from different species. For example, according to the alignments shown in Figure 9, at certain residue positions that are fully conserved (*), substitutions, deletions or insertions may not be allowed, while at other positions where one or more residues are not conserved, an amino acid change can be tolerated. Residues that are semi-conserved (.) may tolerate changes that preserve charge, polarity, and/or size.

[00161] Habp2 Peptides are active fragments containing contiguous amino acid residues derived from the full-length Habp2 polypeptide. In Figure 9, the regions encompassing the human peptides and the murine peptides are highlighted in gray.

[00162] The length of contiguous amino acid residues of a peptide or a polypeptide subsequence varies depending on the specific naturally-occurring amino acid sequence from which the subsequence is derived. In general, peptides and polypeptides may be from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 40 amino acids, from about 40 amino acids to about 50 amino acids, from about 50 amino acids to about 75 amino acids, from about 75 amino acids to about 100 amino acids, from about 100 amino acids to about 150 amino acids, from about 150 amino acids to about 200 amino acids, or from about 200 amino acids up to the full-length peptide or polypeptide. Peptides have a length that is less than the full length of the naturally-occurring polypeptide. [00163] In some embodiments, the Habp2 Peptides can have a length of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 35 amino acids, from about 40 amino acids to about 45 amino acids, from about 45 amino acids to about 50 amino acids, or from more than about 50 amino acids. In certain embodiments, the peptides contemplated by the present disclosure are less than about 25 amino acids in length (see Figure 9).

[00164] Additionally, the Habp2 Peptides can have a defined sequence identity compared to a reference sequence over a defined length of contiguous amino acids (e.g., a "comparison window"). Methods of alignment of sequences for comparison are well-known in the art.

Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482 (1981), by the homology alignment algorithm of Needleman & Wunsch, J. Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson & Lipman, Proc. Nat'l. Acad. Sci. USA 85:2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by manual alignment and visual inspection (see, e.g., Current Protocols in Molecular Biology (Ausubel et al, eds. 1995 supplement)).

[00165] As an example, a suitable Habp2 Peptide can comprise an amino acid sequence having at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%), at least about 98%), or at least about 99%, amino acid sequence identity to a contiguous stretch of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 12 amino acids, from about 12 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 22 amino acids, or from about 22 amino acids to about 24 amino acids of one of the following reference amino acid sequences:

PGVYTQVTKFLNWIKATIKSESGF (SEQ ID NO: 58);

PGVYTQVAKFLNWIKATIQKGSSF (SEQ ID NO: 59);

PGVYTQVTKFLNWIKTTMHREAGL (SEQ ID NO: 60); or

PGVYTQVTKFLNWIKTTMHKEAGL (SEQ ID NO: 61). [00166] For example, in some embodiments, a suitable Habp2 Peptide can comprise an amino acid sequence having at least about 75%, at least about 80%, at least about 85%, at least about 90%), at least about 95%, at least about 98%, or at least about 99%, amino acid sequence identity to the following sequence: PGVYTQVXiKFLNWIKX ₂ TX ₃ X4X ₅ 6 7 8 (SEQ ID NO: 37), where each of X1-X ₉ are semi-conserved residues (where, in some cases, Xi and X ₂ are A or T; X ₃ is I or M; X ₄ is K, Q, or H; X ₅ is S, K, or R; X ₆ is E or G; X ₇ is S or A; X ₈ is S or G; and X is F or L), and where the peptide has a length of from about 5 amino acids to about 50 amino acids, or more than 50 amino acids. For example, the Habp2 Peptide can have a length of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 12 amino acids, from about 12 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 22 amino acids, from about 22 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 35 amino acids, from about 35 amino acids to about 40 amino acids, from about 40 amino acids to about 45 amino acids, from about 45 amino acids to about 50 amino acids, or from more than about 50 amino acids. In some cases, the carboxyl terminal amino acid can be amidated.

[00167] The Habp2 Peptides may be isolated from a natural source (e.g., in an

environment other than its naturally-occurring environment) and also may be recombinantly made (e.g., in a genetically modified host cell such as bacteria; yeast; Pichia; insect cells; and the like), where the genetically modified host cell is modified with a nucleic acid comprising a nucleotide sequence encoding the peptide. The Habp2 Peptides may also be synthetically produced (e.g., by cell-free chemical synthesis). Methods of productions are described in more detail below.

[00168] A Habp2 Peptide may be generated using recombinant techniques to manipulate different Habp2- related nucleic acids known in the art to provide constructs capable of encoding the Habp2 Peptide. It will be appreciated that, when provided a particular amino acid sequence, the ordinary skilled artisan will recognize a variety of different nucleic acid molecules encoding such amino acid sequence in view of her background and experience in, for example, molecular biology.

[00169] Habp2- related nucleic acid sequences and amino acid sequences are known and available in the art and include the following (listed with their corresponding GenBank accession nos).: 1) Homo sapiens: amino acid sequence: NP 004123; nucleotide sequence: NM 004123; amino acid sequence: NP 001171 131; nucleotide sequence: NM 001177660; 2) Rattus norvegicus: amino acid sequence: NP 001001505; nucleotide sequence: NM 001001505; 3) Canis lupus familiaris: amino acid sequence: XP_535016; nucleotide sequence: NM_535016; 4) Pan troglodytes: amino acid sequence: XP 508042; nucleotide sequence: XM 508042; and 5) Mus musculus: amino acid sequence: NP 666213; nucleotide sequence: NM 146101. Exemplary amino acid sequences are depicted in Figures 7A, 7B, 8A, 8B, and 9.

Kazaldl

[00170] "Kazaldl," or "kazal-type serine peptidase inhibitor domain" (also known as

"BONOl"; "IGFBP-related protein 10"; "bone- and odontoblast-expressed gene 1"; "FKSG28"; and "FKSG40") encompasses peptides and variants thereof that are encoded by the Kazaldl gene or homo logs thereof. Kazaldl is found in many mammals, including humans, non-human primates, rodents (e.g., mice), and canines.

[00171] As depicted in Figure 11, Kazaldl gene expression is prevalent in certain EECs of the gastrointestinal tract (e.g., EECs of the duodenum). Figure 13B depicts a sequence alignment of Kazaldl amino acid sequences from the indicated species, including a subsequence of Kazaldl amino acid sequences.

C. Kazaldl Peptide-related Amino Acid and Nucleic Acid Sequences

[00172] Mouse and human Kazaldl peptides have been identified, which peptides are

Kazaldl gene products (Figure 13B). In some cases, a Kazaldl Peptide comprises the following sequence: GWXiRLLAEGEGCAPCRPEX ₂ CAAPRGCLA (SEQ ID NO: 38), where Xi and X ₂ are semi-conserved residues, which resides in some embodiments are as follows: Xi is L or M and X ₂ is E or D.

[00173] Non-limiting examples of Kazaldl peptides are provided below.

GWLRLLAEGEGCAPCRPEECAAPRGCLA (SEQ ID NO: 62); and

GWMRLLAEGEGCAPCRPEECAAPRGCLA (SEQ ID NO: 63).

[00174] Figure 14 indicates the effect of mouse Kazaldl [Murine Peptide-pl :

GWLRLLAEGEGCAPCRPEECAAPRGCLA (SEQ ID NO: 62)] on elevating blood glucose levels and reducing glucose-stimulated insulin secretion. These data were generated as described in the Experimental section. The activity of human Kazaldl [Human Peptide-pl] is predicted to be comparable to that of the corresponding mouse Kazaldl [Murine Peptide-pl] in view of the conservative and semi-conservative nature of the amino acid substitutions.

[00175] While a precise understanding of the Kazaldl Peptides' mechanism of action is not required in order to practice the embodiments of the present disclosure, the increase in systemic glycemia associated with the Kazaldl Peptides is believed to be dependent on reduced insulin concentration. This increase in systemic glycemia is thought to be attributed to one or more physiological responses, including reduced insulin production and/or secretion by pancreatic beta-cells; reduced insulin production and/or secretion due to a secondary messenger (e.g., glucagon or somatostatin); and increased insulin clearance by peripheral tissues, such as the liver.

[00176] As indicated in Figure 14, Kazaldl Peptide increases glucose levels and reduces glucose-stimulated insulin secretion. Kazaldl Peptide increases circulating glucose

concentration, and decreases circulating insulin concentration.

[00177] As used herein, the term "Kazaldl" refers to Kazaldl Peptides of the present disclosure, or fragments thereof, or Kazaldl Nucleic Acid Molecules of the present disclosure, which include their naturally-occurring and non-naturally occurring isoforms, allelic variants and splice variants. As previously noted, a Kazaldl Peptide also refers to peptides that have one or more alterations in the amino acid residues (e.g., at locations that are not conserved across variants or species) while retaining the conserved domains and having the same biological activity as the naturally-occurring Peptides. "Kazaldl" also encompasses nucleic acid sequences that vary in one or more bases from a naturally-occurring DNA sequence but still translate into an amino acid sequence that corresponds to a Peptide due to degeneracy of the genetic code. For example, Kazaldl may refer to amino acid sequences that differ from the naturally-occurring sequences (e.g., naturally-occurring Kazaldl Peptides) by one or more conservative

substitutions, tags, or conjugates.

[00178] Thus, in addition to any naturally-occurring Kazaldl polypeptide (e.g., a Kazaldl

Peptide), the present disclosure contemplates having 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 usually no more than 20, 10, or 5 amino acid substitutions, where the substitution is usually a conservative amino acid substitution. [00179] By "conservative amino acid substitution" generally refers to substitution of amino acid residues within the following groups: 1) L, I, M, V, F; 2) R, K; 3) F, Y, H, W, R; 4) G, A, T, S; 5) Q, N; and 6) D, E. Conservative amino acid substitutions preserve the activity of the protein by replacing an amino acid(s) in the protein with an amino acid with a side chain of similar acidity, basicity, charge, polarity, or size of the side chain. Guidance for substitutions, insertions, or deletions may be based on alignments of amino acid sequences of different variant proteins or proteins from different species. For example, according to the alignments shown in Figure 13B, at certain residue positions that are fully conserved (*), substitutions, deletions or insertions may not be allowed, while at other positions where one or more residues are not conserved, an amino acid change can be tolerated. Residues that are semi-conserved (.) may tolerate changes that preserve charge, polarity, and/or size.

[00180] Kazaldl Peptides are active fragments containing contiguous amino acid residues derived from the full-length Kazaldl polypeptide. In Figure 13B, the regions encompassing the human peptides and the murine peptides are highlighted in gray.

[00181] The length of contiguous amino acid residues of a peptide or a polypeptide subsequence varies depending on the specific naturally-occurring amino acid sequence from which the subsequence is derived. In general, peptides and polypeptides may be from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 28 amino acids, from about 30 amino acids to about 40 amino acids, from about 40 amino acids to about 50 amino acids, from about 50 amino acids to about 75 amino acids, from about 75 amino acids to about 100 amino acids, from about 100 amino acids to about 150 amino acids, from about 150 amino acids to about 200 amino acids, or from about 200 amino acids up to the full-length peptide or polypeptide. Peptides have a length that is less than the full length of the naturally-occurring polypeptide.

[00182] In some embodiments, the Kazaldl Peptides can have a length of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 35 amino acids, from about 40 amino acids to about 45 amino acids, from about 45 amino acids to about 50 amino acids, or from more than about 50 amino acids. In certain embodiments, the peptides contemplated by the present disclosure are less than about 30 amino acids in length (see Figure 13B).

[00183] Additionally, the Kazaldl Peptides can have a defined sequence identity compared to a reference sequence over a defined length of contiguous amino acids (e.g., a "comparison window"). Methods of alignment of sequences for comparison are well-known in the art. Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482 (1981), by the homology alignment algorithm of Needleman & Wunsch, J. Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson & Lipman, Proc. Nat'l. Acad. Sci. USA 85:2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by manual alignment and visual inspection (see, e.g., Current Protocols in Molecular Biology (Ausubel et al, eds. 1995 supplement)).

[00184] As an example, a suitable Kazaldl Peptide can comprise an amino acid sequence having at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%), at least about 98%), or at least about 99%, amino acid sequence identity to a contiguous stretch of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 12 amino acids, from about 12 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, or from about 25 amino acids to 28 amino acids of one of the following reference amino acid sequences:

GWLRLLAEGEGCAPCRPEECAAPRGCLA (SEQ ID NO: 62); or

GWMRLLAEGEGCAPCRPEECAAPRGCLA (SEQ ID NO: 63).

[00185] For example, in some embodiments, a suitable Kazaldl Peptide can comprise an amino acid sequence having at least about 75%, at least about 80%>, at least about 85%, at least about 90%), at least about 95%, at least about 98%, or at least about 99%, amino acid sequence identity to the following sequence: GWXiRLLAEGEGCAPCRPEX ₂ CAAPRGCLA (SEQ ID NO: 38), where Xi and X ₂ are semi-conserved residues (e.g., where Xi is L or M and X ₂ is E or D), and where the peptide has a length of from about 5 amino acids to about 50 amino acids, or more than 50 amino acids. For example, the Kazaldl Peptide can have a length of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 12 amino acids, from about 12 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 28 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 35 amino acids, from about 35 amino acids to about 40 amino acids, from about 40 amino acids to about 45 amino acids, from about 45 amino acids to about 50 amino acids, or from more than about 50 amino acids. In some cases, the carboxyl terminal amino acid can be amidated.

[00186] The Kazaldl Peptides may be isolated from a natural source (e.g., in an environment other than its naturally-occurring environment) and also may be recombinantly made (e.g., in a genetically modified host cell such as bacteria; yeast; Pichia; insect cells; and the like), where the genetically modified host cell is modified with a nucleic acid comprising a nucleotide sequence encoding the peptide. The Kazaldl Peptides may also be synthetically produced (e.g., by cell-free chemical synthesis). Methods of productions are described in more detail below.

[00187] A Kazaldl Peptide may be generated using recombinant techniques to manipulate different Kazaldl- related nucleic acids known in the art to provide constructs capable of encoding the Kazaldl Peptide. It will be appreciated that, when provided a particular amino acid sequence, the ordinary skilled artisan will recognize a variety of different nucleic acid molecules encoding such amino acid sequence in view of her background and experience in, for example, molecular biology.

[00188] Kazaldl - related nucleic acid sequences and amino acid sequences are known and available in the art and include the following (listed with their corresponding GenBank accession nos).: 1) Homo sapiens: amino acid sequence: NP l 12191; nucleotide sequence: NM 030929; 2) Rattus norvegicus: amino acid sequence: NP 001028236; nucleotide sequence:

NM 001033064; 3) Canis lupus familiaris: amino acid sequence: NP 851650; nucleotide sequence: NM_846557; 4) Pan troglodytes: amino acid sequence: XP_001 169573; nucleotide sequence: XM 001169573; and 5) Mus musculus: amino acid sequence: NP 849260; nucleotide sequence: NM_178929. Exemplary amino acid sequences are depicted in Figures 12A, 12B, 13 A, and 13B. Respl8

[00189] "Res l8," or "regulated endocrine-specific protein 18" encompasses peptides and variants thereof that are encoded by the Respl8 gene or homo logs thereof. Respl8 is found in many mammals, including humans, non-human primates, rodents (e.g., mice), and canines.

[00190] As depicted in Figure 15, Respl8 gene expression is prevalent in EECs of the gastrointestinal tract. Figure 18 depicts a sequence alignment of Respl8 amino acid sequences from the indicated species, including a subsequence of Respl8 amino acid sequences.

D. Resp 18 Peptide-related Amino Acid and Nucleic Acid Sequences

[00191] Mouse and human Resp 18 peptides have been identified, which peptides are Resp 18 gene products (Figure 18). In some cases, a Resp 18 Peptide comprises the following sequence: XiX ₂ CFTX ₃ X4VX ₅ X6KX7 8 io ii i2 i3 i4P( )n (SEQ ID NO: 39), where X X ₅ , X7-X ₁₂ , and Xi ₄ are semi-conserved residues; where X ₆ is P, L, or S; where X ₁₃ is T, K, or A; where X ₁₄ is H, T, or N; and where n is an integer from 1 to 5 (e.g., 1, 2, 3, 4, or 5) and X is any amino acid, wherein in some embodiments the following residues are as follows: Xi is D or E; X ₂ is R or Q; X is T or S; X4 is K or E; X ₅ is I, D, or V; X ₇ is A or T; Xg is T or L; X ₉ is K or E; X ₁₀ is I or Q; Xn is E or H; and X ₁₂ is A, V, or I. In some cases, (X) _n can be T, S, IV, or VKITY.

[00192] Non- limiting examples of Resp 18 peptides are provided below.

DRCFTTKVIPKATKQEATHPT (SEQ ID NO: 64);

DRCFTTKVIPKATKQEVTHPS (SEQ ID NO: 65);

EQCFTSKVDLKTLEIHIKTPIV (SEQ ID NO: 66);

DQCFTSKVVSKALKQEVANPVKITYR (SEQ ID NO: 67); and

DQCFTSEVVSKALKQEVANP VKITY (SEQ ID NO: 68).

[00193] Figure 19 indicates the effect of a mouse Resp 18 [Murine Peptide-pl :

DRCFTTKVIPKATKQEATHPT (SEQ ID NO: 64)] on elevating blood glucose levels and reducing glucose-stimulated insulin secretion. These data were generated as described in the Experimental section. The activity of human Resp 18 [Human Peptide-pl] is predicted to be comparable to that of the corresponding mouse [Murine Peptide-pl] in view of the conservative and semi-conservative nature of the amino acid substitutions. [00194] While a precise understanding of the Respl8 Peptides' mechanism of action is not required in order to practice the embodiments of the present disclosure, the increase in systemic glycemia associated with the Respl8 Peptides is believed to be dependent on reduced insulin concentration. This increase in systemic glycemia is thought to be attributed to one or more physiological responses, including reduced insulin production and/or secretion by pancreatic beta-cells; reduced insulin production and/or secretion due to a secondary messenger (e.g., glucagon or somatostatin); and increased insulin clearance by peripheral tissues, such as the liver.

[00195] As indicated in Figure 18, Respl8 Peptide increases glucose levels and reduces glucose-stimulated insulin secretion. Respl8 Peptide increases circulating glucose concentration, and decreases circulating insulin concentration.

[00196] As used herein, the term "Resp 18" refers to Resp 18 Peptides of the present disclosure, or fragments thereof, or Resp 18 Nucleic Acid Molecules of the present disclosure, which include their naturally-occurring and non-naturally occurring isoforms, allelic variants and splice variants. As previously noted, a Resp 18 Peptide also refers to peptides that have one or more alterations in the amino acid residues (e.g., at locations that are not conserved across variants or species) while retaining the conserved domains and having the same biological activity as the naturally-occurring Peptides. "Resp 18" also encompasses nucleic acid sequences that vary in one or more bases from a naturally-occurring DNA sequence but still translate into an amino acid sequence that corresponds to a Peptide due to degeneracy of the genetic code. For example, Resp 18 may refer to amino acid sequences that differ from the naturally-occurring sequences (e.g., Respl8 Peptides) by one or more conservative substitutions, tags, or conjugates.

[00197] Thus, in addition to any naturally-occurring Respl8 polypeptide (e.g., a Respl8

Peptide), the present disclosure contemplates having 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 usually no more than 20, 10, or 5 amino acid substitutions, where the substitution is usually a conservative amino acid substitution.

[00198] By "conservative amino acid substitution" generally refers to substitution of amino acid residues within the following groups: 1) L, I, M, V, F; 2) R, K; 3) F, Y, H, W, R; 4) G, A, T, S; 5) Q, N; and 6) D, E. Conservative amino acid substitutions preserve the activity of the protein by replacing an amino acid(s) in the protein with an amino acid with a side chain of similar acidity, basicity, charge, polarity, or size of the side chain. Guidance for substitutions, insertions, or deletions may be based on alignments of amino acid sequences of different variant proteins or proteins from different species. For example, according to the alignments shown in Figure 18, at certain residue positions that are fully conserved (*), substitutions, deletions or insertions may not be allowed, while at other positions where one or more residues are not conserved, an amino acid change can be tolerated. Residues that are semi-conserved (.) may tolerate changes that preserve charge, polarity, and/or size.

[00199] Respl8 Peptides are active fragments containing contiguous amino acid residues derived from the full-length Respl8 polypeptide. In Figure 19, the regions encompassing the human peptides and the murine peptides are highlighted in gray.

[00200] The length of contiguous amino acid residues of a peptide or a polypeptide subsequence varies depending on the specific naturally-occurring amino acid sequence from which the subsequence is derived. In general, peptides and polypeptides may be from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 28 amino acids, from about 30 amino acids to about 40 amino acids, from about 40 amino acids to about 50 amino acids, from about 50 amino acids to about 75 amino acids, from about 75 amino acids to about 100 amino acids, from about 100 amino acids to about 150 amino acids, from about 150 amino acids to about 200 amino acids, or from about 200 amino acids up to the full-length peptide or polypeptide. Peptides have a length that is less than the full length of the naturally-occurring polypeptide.

[00201] In some embodiments, the Respl8 Peptides can have a length of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 35 amino acids, from about 40 amino acids to about 45 amino acids, from about 45 amino acids to about 50 amino acids, or from more than about 50 amino acids. In certain embodiments, the peptides contemplated by the present disclosure are less than about 30 amino acids in length (see Figure 18).

[00202] Additionally, the Respl8 Peptides can have a defined sequence identity compared to a reference sequence over a defined length of contiguous amino acids (e.g., a "comparison window"). Methods of alignment of sequences for comparison are well-known in the art. Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482 (1981), by the homology alignment algorithm of Needleman & Wunsch, J. Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson & Lipman, Proc. Nat'l. Acad. Sci. USA 85 :2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by manual alignment and visual inspection (see, e.g., Current Protocols in Molecular Biology (Ausubel et al, eds. 1995 supplement)).

[00203] As an example, a suitable Respl 8 Peptide can comprise an amino acid sequence having at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%), at least about 98%), or at least about 99%, amino acid sequence identity to a contiguous stretch of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 12 amino acids, from about 12 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, or from about 20 amino acids to about 25 amino acids, of one of the following reference amino acid sequences:

DRCFTTKVIPKAT QEATHPT (SEQ ID NO: 64);

DRCFTTKVIPKATKQEVTHPS (SEQ ID NO: 65);

EQCFTSKVDLKTLEIHIKTPIV (SEQ ID NO: 66);

DQCFTSKVVSKALKQEVANPVKITYR (SEQ ID NO: 67); and

DQCFTSEVVSKALKQEVANP VKITY (SEQ ID NO: 68).

[00204] For example, in some embodiments, a suitable Respl 8 Peptide can comprise an amino acid sequence having at least about 75%, at least about 80%>, at least about 85%, at least about 90%), at least about 95%, at least about 98%, or at least about 99%, amino acid sequence identity to the following sequence: XiX ₂ CFTX ₃ X ₄ VX ₅ X ₆ KX ₇ X ₈ X ₉ XioXiiXi2Xi3Xi4P(X)n (SEQ ID NO: 39) (where X ₁ -X5, X ₇ -X ₁₂ , and X ₁₄ are semi-conserved residues; where X ₆ is P, L, or S; where X ₁₃ is T, K, or A; where X ₁₄ is H, T, or N; and where n is an integer from 1 to 5 (e.g., 1 , 2, 3, 4, or 5) and X is any amino acid; e.g., where Xi is D or E; X ₂ is R or Q; X ₃ is T or S; X ₄ is K or E; X ₅ is I, D, or V; X ₇ is A or T; X ₈ is T or L; X ₉ is K or E; X ₁₀ is I or Q; X _n is E or H; and X ₁₂ is A, V, or I; e.g., where (X) _n can be T, S, IV, or VKITY), and where the peptide has a length of from about 5 amino acids to about 50 amino acids, or more than 50 amino acids. For example, the Respl 8 Peptide can have a length of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 12 amino acids, from about 12 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 28 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 35 amino acids, from about 35 amino acids to about 40 amino acids, from about 40 amino acids to about 45 amino acids, from about 45 amino acids to about 50 amino acids, or from more than about 50 amino acids. In some cases, the carboxyl terminal amino acid can be amidated.

[00205] The Respl8 Peptides may be isolated from a natural source (e.g., in an environment other than its naturally-occurring environment) and also may be recombinantly made (e.g., in a genetically modified host cell such as bacteria; yeast; Pichia; insect cells; and the like), where the genetically modified host cell is modified with a nucleic acid comprising a nucleotide sequence encoding the peptide. The Respl8 Peptides may also be synthetically produced (e.g., by cell-free chemical synthesis). Methods of productions are described in more detail below.

[00206] A Resp 18 Peptide may be generated using recombinant techniques to manipulate different Resp 18- related nucleic acids known in the art to provide constructs capable of encoding the Resp 18 Peptide. It will be appreciated that, when provided a particular amino acid sequence, the ordinary skilled artisan will recognize a variety of different nucleic acid molecules encoding such amino acid sequence in view of her background and experience in, for example, molecular biology.

[00207] Resp 18- related nucleic acid sequences and amino acid sequences are known and available in the art and include the following (listed with their corresponding GenBank accession nos).: 1) Homo sapiens: amino acid sequence: NP 001007090; nucleotide sequence:

NM 001007089; 2) Rattus norvegicus: amino acid sequence: NP 062151; nucleotide sequence: NM_019278; and 3) Mus musculus: amino acid sequence: NP_0033075; nucleotide sequence: NM 009049. Exemplary amino acid sequences are depicted in Figures 16, 17, and 18.

Tinag

[00208] "Tinag," or "tubulointerstitial nephritis antigen" encompasses peptides and variants thereof that are encoded by the Tinag gene or homologs thereof. Tinag is found in many mammals, including humans, non-human primates, rodents (e.g., mice), and canines. [00209] As depicted in Figure 20, Tinag gene expression is prevalent in certain EECs of the gastrointestinal tract (e.g., EECs of the duodenum and ileum) and is also observed in certain ECs of the gastrointestinal tract (ECs of the duodenum). Figure 23 depicts a sequence alignment of Tinag amino acid sequences from the indicated species, including a subsequence of Tinag amino acid sequences.

E. Tinag Peptide-related Amino Acid and Nucleic Acid Sequences

[00210] Mouse and human Tinag peptides have been identified, which peptides are Tinag gene products (Figure 23). In some cases, a Tinag Peptide comprises the following sequence: LX ₁ THAVKLTGWGTLX ₂ GAX3GX ₄ KEKFWIAANSWG (SEQ ID NO: 41), where X _h X ₂ , X ₃ , and X ₄ are semi-conserved residues, which residues in some embodiments are as follows: each of Xi, X ₂ , X ₃ , and X ₄ is independently R, Q, or K. In some cases, Xi is R or Q; X ₂ is R or K; X ₃ is R or Q; and X ₄ is Q or K. Non- limiting examples of Tinag peptides are provided below.

LQTHAVKLTGWGTLRGAQGQKEKFWIAANSWG (SEQ ID NO: 42);

LRTHAVKLTGWGTLRGARGKKEKFWIAANSWG (SEQ ID NO: 44);

LQTHAVKLTGWGTLRGAQGQKEKFWIAANSWG-COOH (SEQ ID NO: 42);

LQTHAVKLTGWGTLRGAQGQKEKFWIAANSW-CONH ₂ (SEQ ID NO: 43);

LRTHAVKLTGWGTLRGARGKKEKFWIAANSWG-COOH (SEQ ID NO: 44); and

LRTHAVKLTGWGTLRGARGKKEKFWIAANSW-CONH ₂ (SEQ ID NO: 45).

[00211] Figures 24 and 25 indicate the effect of mouse Tinag Peptides p3 and p4 [Murine

Peptide-p3: LRTHAVKLTGWGTLRGARGKKEKFWIAANSWG-COOH (SEQ ID NO: 44); and Murine Peptide-p4: LRTHAVKLTGWGTLRGARGKKEKFWIAANSW-CONH ₂ (SEQ ID NO: 45)], respectively, on elevating blood glucose levels and reducing glucose-stimulated insulin secretion. These data were generated as described in the Experimental section. The activity of Human Tinag Peptides is predicted to be comparable to that of the corresponding Murine (mouse) Peptide in view of the conservative and semi-conservative nature of the amino acid substitutions.

[00212] While a precise understanding of the Tinag Peptides' mechanism of action is not required in order to practice the embodiments of the present disclosure, the increase in systemic glycemia associated with the Tinag Peptides is believed to be dependent on reduced insulin concentration. This increase in systemic glycemia is thought to be attributed to one or more physiological responses, including reduced insulin production and/or secretion by pancreatic beta-cells; reduced insulin production and/or secretion due to a secondary messenger (e.g., glucagon or somatostatin); and increased insulin clearance by peripheral tissues, such as the liver.

[00213] As indicated in Figures 24 and 25, the mouse Tinag peptides [Murine Peptide-p3 and Murine Peptide-p4] increase circulating glucose concentration and decrease circulating insulin concentration.

[00214] As used herein, the term "Tinag" refers to Tinag Peptides of the present disclosure, or fragments thereof, or Tinag Nucleic Acid Molecules of the present disclosure, which include their naturally-occurring and non-naturally occurring isoforms, allelic variants and splice variants. As previously noted, a Tinag Peptide also refers to peptides that have one or more alterations in the amino acid residues (e.g., at locations that are not conserved across variants or species) while retaining the conserved domains and having the same biological activity as the naturally-occurring Peptides. "Tinag" also encompasses nucleic acid sequences that vary in one or more bases from a naturally-occurring DNA sequence but still translate into an amino acid sequence that corresponds to a Peptide due to degeneracy of the genetic code. For example, Tinag may refer to amino acid sequences that differ from the naturally-occurring sequences (e.g., naturally-occurring Tinag Peptides) by one or more conservative substitutions, tags, or conjugates.

[00215] Thus, in addition to any naturally-occurring Tinag polypeptide (e.g., a Tinag

Peptide), the present disclosure contemplates having 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 usually no more than 20, 10, or 5 amino acid substitutions, where the substitution is usually a conservative amino acid substitution.

[00216] By "conservative amino acid substitution" generally refers to substitution of amino acid residues within the following groups: 1) L, I, M, V, F; 2) R, K; 3) F, Y, H, W, R; 4) G, A, T, S; 5) Q, N; and 6) D, E. Conservative amino acid substitutions preserve the activity of the protein by replacing an amino acid(s) in the protein with an amino acid with a side chain of similar acidity, basicity, charge, polarity, or size of the side chain. Guidance for substitutions, insertions, or deletions may be based on alignments of amino acid sequences of different variant proteins or proteins from different species. For example, according to the alignments shown in Figure 23, at certain residue positions that are fully conserved (*), substitutions, deletions or insertions may not be allowed, while at other positions where one or more residues are not conserved, an amino acid change can be tolerated. Residues that are semi-conserved (.) may tolerate changes that preserve charge, polarity, and/or size.

[00217] Tinag Peptides are active fragments containing contiguous amino acid residues derived from the full-length Tinag polypeptide. In Figure 23, the regions encompassing the human peptides and the murine peptides are highlighted in gray.

[00218] The length of contiguous amino acid residues of a peptide or a polypeptide subsequence varies depending on the specific naturally-occurring amino acid sequence from which the subsequence is derived. In general, peptides and polypeptides may be from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 40 amino acids, from about 40 amino acids to about 50 amino acids, from about 50 amino acids to about 75 amino acids, from about 75 amino acids to about 100 amino acids, from about 100 amino acids to about 150 amino acids, from about 150 amino acids to about 200 amino acids, or from about 200 amino acids up to the full-length peptide or polypeptide. Peptides have a length that is less than the full length of the naturally-occurring polypeptide.

[00219] In some embodiments, the Tinag Peptides can have a length of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 35 amino acids, from about 40 amino acids to about 45 amino acids, from about 45 amino acids to about 50 amino acids, or from more than about 50 amino acids. In certain embodiments, the peptides contemplated by the present disclosure are less than about 30 amino acids in length (see Figure 23).

[00220] Additionally, the Tinag Peptides can have a defined sequence identity compared to a reference sequence over a defined length of contiguous amino acids (e.g., a "comparison window"). Methods of alignment of sequences for comparison are well-known in the art.

Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482 (1981), by the homology alignment algorithm of Needleman & Wunsch, J. Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson & Lipman, Proc. Nat'l. Acad. Sci. USA 85 :2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by manual alignment and visual inspection (see, e.g., Current Protocols in Molecular Biology (Ausubel et al, eds. 1995 supplement)).

[00221] As an example, a suitable Tinag Peptide can comprise an amino acid sequence having at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 98%), or at least about 99%, amino acid sequence identity to a contiguous stretch of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 12 amino acids, from about 12 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, or from about 30 amino acids to 33 amino acids, of one of the following reference amino acid sequences:

LQTHAVKLTGWGTLPvGAQGQKEKFWIAANSWG (SEQ ID NO: 42);

LRTHAVKLTGWGTLPvGAPvGKKEKFWIAANSWG (SEQ ID NO: 44);

LQTHAVKLTGWGTLRGAQGQKEKFWIAANSWG-COOH (SEQ ID NO: 42);

LQTHAVKLTGWGTLRGAQGQKEKFWIAANSW-CONH ₂ (SEQ ID NO: 43);

LRTHAVKLTGWGTLRGARGKKEKFWIAANSWG-COOH (SEQ ID NO: 44); and

LRTHAVKLTGWGTLRGARGKKEKFWIAANSW-CONH ₂ (SEQ ID NO: 45).

[00222] For example, in some embodiments, a suitable Tinag Peptide can comprise an amino acid sequence having at least about 75%, at least about 80%>, at least about 85%, at least about 90%), at least about 95%, at least about 98%, or at least about 99%), amino acid sequence identity to the following sequence: LXiTHAVKLTGWGTLX ₂ GAX ₃ GX ₄ KEKFWIAANSWG (SEQ ID NO: 41), where Xi, X ₂ , X ₃ , and X ₄ are semi-conserved residues (e.g., where each of Xi, X ₂ , X ₃ , and X ₄ is independently R, Q, or K; e.g., where Xi is R or Q; X2 is R or K; X ₃ is R or Q; and X ₄ is Q or K), and where the peptide has a length of from about 5 amino acids to about 50 amino acids, or more than 50 amino acids. For example, the Tinag Peptide can have a length of from about 5 amino acids to about 10 amino acids, from about 10 amino acids to about 12 amino acids, from about 12 amino acids to about 15 amino acids, from about 15 amino acids to about 20 amino acids, from about 20 amino acids to about 25 amino acids, from about 25 amino acids to about 30 amino acids, from about 30 amino acids to about 33 amino acids, from about 30 amino acids to about 35 amino acids, from about 35 amino acids to about 40 amino acids, from about 40 amino acids to about 45 amino acids, from about 45 amino acids to about 50 amino acids, or from more than about 50 amino acids. In some cases, the carboxyl terminal amino acid can be amidated.

[00223] The Tinag Peptides may be isolated from a natural source (e.g., in an environment other than its naturally-occurring environment) and also may be recombinantly made (e.g., in a genetically modified host cell such as bacteria; yeast; Pichia; insect cells; and the like), where the genetically modified host cell is modified with a nucleic acid comprising a nucleotide sequence encoding the peptide. The Tinag Peptides may also be synthetically produced (e.g., by cell-free chemical synthesis). Methods of productions are described in more detail below.

[00224] A Tinag Peptide may be generated using recombinant techniques to manipulate different Tinag-related nucleic acids known in the art to provide constructs capable of encoding the Tinag Peptide. It will be appreciated that, when provided a particular amino acid sequence, the ordinary skilled artisan will recognize a variety of different nucleic acid molecules encoding such amino acid sequence in view of her background and experience in, for example, molecular biology.

[00225] Tinag- related nucleic acid sequences and amino acid sequences encoding are known and available in the art and include the following (listed with their corresponding

GenBank accession nos).: 1) Homo sapiens: amino acid sequence: NP 055279; nucleotide sequence: NM 014464; 2) Rattus norvegicus: amino acid sequence: NP 001005549; nucleotide sequence: NM 001005549; 3) Canis lupus familiaris: amino acid sequence: XP 538969;

nucleotide sequence: XM 538969; 4) Pan troglodytes: amino acid sequence: XP 518550;

nucleotide sequence: XM 518550; and S) Mus musculus: amino acid sequence: NP 036163; nucleotide sequence: NM 012033. Exemplary amino acid sequences are depicted in Figures 21, 22, and 23.

MODULATORS

[00226] The term "Modulators" refers to both "Inhibitors" and "Activators" of the

Peptides and/or the activity thereof. [00227] As described above, the Peptides (e.g., Ednl Peptides; Habp2 Peptides; Kazaldl Peptides; Respl8 Peptides; and Tinag Peptides), for example, elevate blood glucose levels and reduce glucose-stimulated insulin secretion. The Inhibitors contemplated by the present disclosure counteract these effects by, for example, acting to partially or totally block

stimulation, decrease, prevent, delay activation, inactivate, desensitize, or antagonize or down- regulate the effects of the Peptides.

[00228] In some embodiments, the Inhibitor is an antibody that is capable of eliminating or significantly reducing an effector function of a target antigen (e.g., an Invention Peptide) to which it binds. An antibody useful according to the present disclosure can be generated by a skilled artisan using routine techniques. For example, one or more antibodies to known antigens may be generated and then evaluated to select at least one with the desired properties.

Thereafter, one or more antibodies can be produced and formulated in a manner suitable for administration to a subject.

[00229] In other embodiments, the Inhibitor is a small molecule antagonist compound, antibody-related molecule, or other bioorganic molecule that binds or otherwise blocks (e.g., at or around a Peptide binding site) a Peptide from having its normal endogenous effect. Numerous libraries of small molecule compounds (e.g., combinatorial libraries) are commercially available and can serve as a starting point for identifying an Inhibitor. The skilled artisan is able to develop one or more assays (e.g., biochemical or cell-based assays) in which such compound libraries can be screened in order to identify one or more compounds having the desired properties; thereafter, the skilled medicinal chemist is able to optimize such one or more compounds by, for example, synthesizing and evaluating analogs and derivatives thereof.

Synthetic and/or molecular modeling studies can also be utilized in the identification of an Inhibitor.

[00230] In still further embodiments, the Inhibitor is an antagonistic peptide structurally distinguishable from the Peptides (e.g., a peptide variant having one or more amino acid deletions, insertions or non-conservative substitutions compared to the Peptides) capable of binding to a receptor (or other effector of activity), but deficient in its ability to mediate a biological response. One of ordinary skill in the art is knowledgeable about techniques for generating antagonistic peptides having desired properties. For example, the amino acid sequences of the Peptides can be systematically modified by making one or more amino acid deletions, insertions or non-conservative substitutions and then evaluating the activity of the resulting peptides as described in the Examples that follow or in other experimental settings known to the skilled artisan.

[00231] When a subject is hypoglycemic or suffers from a disease, disorder or condition involving decreased blood glucose levels, increased glucose-stimulated insulin secretion, and/or similar effects, it may be appropriate to administer an agent capable of elevating blood glucose. Thus, some embodiments of the present disclosure contemplate the use of Activators that include, for example, agents that stimulate, increase, activate, facilitate, enhance activation, sensitize or agonize or up-regulate the function or activity of one or more Peptides.

[00232] In some embodiments, the Activator is a Peptide described herein. In other embodiments, the Activator is an agonistic peptide structurally distinguishable from the Peptides (e.g., a variant peptide having one or more amino acid deletions, insertions or non-conservative substitutions compared to the Peptides) but having comparable activity. The skilled artisan is able to identify agonistic peptides having desired properties using methodologies similar to those set forth above for antagonist antibodies.

[00233] In other embodiments, the Activator is a small molecule agonist compound having activity similar to glucagon (GLUCAGEN), a linear peptide of 29 amino acids. Parenteral administration of glucagon activates hepatic gluconeogenesis and stimulates the breakdown of glycogen stored in the liver, causing an increase in blood glucose levels. As generally described above in the context of small molecule antagonist compounds and other bioorganic molecules, a skilled medicinal chemist is able to utilize known techniques to identify and optimize a small molecule agonist or other bioorganic molecule having the desired properties. The present disclosure envisions agonists that are both structurally related and unrelated to glucagon and analogs and derivatives thereof.

[00234] In still further embodiments, the Activator is an antibody that mimics, in whole or in part, the activity of the Peptides. The generation and use of such antibodies is known in the art (see, e.g., Kifor et al, JCEM (2004) 89(2): 548-56; Dragun et al, NEJM (2005) 352:558-69).

Amide Bond Substitutions

[00235] In some cases, a Peptide (e.g., an Ednl Peptide; a Habp2 Peptide; a Kazaldl

Peptide; a Respl8 Peptide; or a Tinag Peptide), includes one or more linkages other than peptide bonds, e.g., at least two adjacent amino acids are joined via a linkage other than an amide bond. For example, in order to reduce or eliminate undesired proteolysis or other means of degradation, and/or to increase serum stability, and/or to restrict or increase conformational flexibility, one or more amide bonds within the backbone of a Peptide can be substituted.

[00236] In another example, one or more amide linkages (-CO-NH-) in a Peptide can be replaced with a linkage which is an isostere of an amide linkage, such as -CH2NH-, CH ₂ S-, - CH ₂ CH ₂ -, -CH=CH-(cis and trans), -COCH ₂ -, -CH(OH)CH ₂ - or -CH ₂ SO-. One or more amide linkages in an Invention Peptide can also be replaced by, for example, a reduced isostere pseudopeptide bond. See Couder et al. (1993) Int. J. Peptide Protein Res. 41 : 181-184. Such replacements and how to effect them are known to those of ordinary skill in the art.

Amino Acid Substitutions

[00237] One or more amino acid substitutions can be made in a Peptide (e.g., an Ednl

Peptide; a Habp2 Peptide; a Kazaldl Peptide; a Respl8 Peptide; or a Tinag Peptide). The following are non- limiting examples:

[00238] a) substitution of alkyl-substituted hydrophobic amino acids, including alanine, leucine, isoleucine, valine, norleucine, (S)-2-aminobutyric acid, (S)-cyclohexylalanine or other simple alpha-amino acids substituted by an aliphatic side chain from C1-C10 carbons including branched, cyclic and straight chain alkyl, alkenyl or alkynyl substitutions;

[00239] b) substitution of aromatic-substituted hydrophobic amino acids, including phenylalanine, tryptophan, tyrosine, sulfotyrosine, biphenylalanine, 1-naphthylalanine, 2- naphthylalanine, 2-benzothienylalanine, 3-benzothienylalanine, histidine, including amino, alkylamino, dialkylamino, aza, halogenated (fluoro, chloro, bromo, or iodo) or alkoxy (from Ci- C4)-substituted forms of the above-listed aromatic amino acids, illustrative examples of which are: 2-, 3- or 4-aminophenylalanine, 2-, 3- or 4-chlorophenylalanine, 2-, 3- or 4- methylphenylalanine, 2-, 3- or 4-methoxyphenylalanine, 5-amino-, 5-chloro-, 5-methyl- or 5- methoxytryptophan, 2'-, 3'-, or 4'-amino-, 2'-, 3'-, or 4'-chloro-, 2, 3, or 4-biphenylalanine, 2'-, 3'-, or 4'-methyl-, 2-, 3- or 4-biphenylalanine, and 2- or 3-pyridylalanine;

[00240] c) substitution of amino acids containing basic side chains, including arginine, lysine, histidine, ornithine, 2,3-diaminopropionic acid, homoarginine, including alkyl, alkenyl, or aryl-substituted (from C ₁ -C ₁₀ branched, linear, or cyclic) derivatives of the previous amino acids, whether the substituent is on the heteroatoms (such as the alpha nitrogen, or the distal nitrogen or nitrogens, or on the alpha carbon, in the pro-R position for example. Compounds that serve as illustrative examples include: N-epsilon-isopropyl-lysine, 3-(4-tetrahydropyridyl)-glycine, 3-(4- tetrahydropyridyl)-alanine, Ν,Ν-gamma, gamma'-diethyl-homoarginine. Included also are compounds such as alpha-methyl-arginine, alpha-methyl-2,3-diaminopropionic acid, alpha- methyl-histidine, alpha-methyl-ornithine where the alkyl group occupies the pro-R position of the alpha-carbon. Also included are the amides formed from alkyl, aromatic, heteroaromatic (where the heteroaromatic group has one or more nitrogens, oxygens or sulfur atoms singly or in combination) carboxylic acids or any of the many well-known activated derivatives such as acid chlorides, active esters, active azolides and related derivatives) and lysine, ornithine, or 2,3- diaminopropionic acid;

[00241] d) substitution of acidic amino acids, including aspartic acid, glutamic acid, homoglutamic acid, tyrosine, alkyl, aryl, arylalkyl, and heteroaryl sulfonamides of 2,4- diaminopriopionic acid, ornithine or lysine and tetrazole-substituted alkyl amino acids;

[00242] e) substitution of side chain amide residue, including asparagine, glutamine, and alkyl or aromatic substituted derivatives of asparagine or glutamine; and

[00243] f) substitution of hydroxyl containing amino acids, including serine, threonine, homoserine, 2,3-diaminopropionic acid, and alkyl or aromatic substituted derivatives of serine or threonine.

[00244] In some cases, a Peptide comprises one or more naturally occurring non- genetically encoded L-amino acids, synthetic L-amino acids or D-enantiomers of an amino acid. For example, a Peptide can comprise only D-amino acids. For example, a Peptide can comprise one or more of the following residues: hydroxyproline, β-alanine, o-aminobenzoic acid, m- aminobenzoic acid, p-aminobenzoic acid, m-aminomethylbenzoic acid, 2,3-diaminopropionic acid, a-aminoisobutyric acid, N-methylglycine (sarcosine), ornithine, citrulline, t-butylalanine, t- butylglycine, N-methylisoleucine, phenylglycine, cyclohexylalanine, norleucine,

naphthylalanine, pyridylalanine 3-benzothienyl alanine, 4-chlorophenylalanine, 2- fluorophenylalanine, 3-fluorophenylalanine, 4-fluorophenylalanine, penicillamine, 1,2,3,4- tetrahydroisoquinoline-3 -carboxylic acid, β-2-thienylalanine, methionine sulfoxide,

homoarginine, N-acetyl lysine, 2,4-diamino butyric acid, rho-aminophenylalanine, N- methylvaline, homocysteine, homoserine, ε-amino hexanoic acid, ω-aminohexanoic acid, ω- aminoheptanoic acid, ω-aminooctanoic acid, ω-aminodecanoic acid, ω-aminotetradecanoic acid, cyclohexylalanine, α,γ-diaminobutyric acid, α,β-diaminopropionic acid, δ-amino valeric acid, and 2,3-diaminobutyric acid.

Additional modifications

[00245] A cysteine residue or a cysteine analog can be introduced into a Peptide (e.g., an

Ednl Peptide; a Habp2 Peptide; a Kazaldl Peptide; a Respl8 Peptide; or a Tinag Peptide) to provide for linkage to another peptide via a disulfide linkage or to provide for cyclization of the Peptide. Methods of introducing a cysteine or cysteine analog are known in the art; see, e.g., U.S. Patent No. 8,067,532.

[00246] A Peptide can be cyclized. One or more cysteine or cysteine analogs can be introduced into a Peptide, where the introduced cysteine or cysteine analog can form a disulfide bond with a second introduced cysteine or cysteine analog. Other means of cyclization include introduction of an oxime linker or a lanthionine linker; see, e.g., U.S. Patent No. 8,044,175. Any combination of amino acids (or non-amino acid moiety) that can form a cyclizing bond can be used and/or introduced. A cyclizing bond can be generated with any combination of amino acids (or with amino acid and -(CH ₂ ) _n -CO- or -(CH ₂ ) _n -C ₆ H ₄ -CO-) with functional groups which allow for the introduction of a bridge. Some examples are disulfides, disulfide mimetics such as the - (CH ₂ ) _n - carba bridge, thioacetal, thioether bridges (cystathionine or lanthionine) and bridges containing esters and ethers. In these examples, n can be any integer, but is frequently less than ten.

[00247] Other modifications include, for example, an N-alkyl (or aryl) substitution or backbone crosslinking to construct lactams and other cyclic structures. Other derivatives of the modulator compounds of the presen disclosure include C-terminal

hydroxymethyl derivatives, O-modified derivatives (e.g., C-terminal hydroxymethyl benzyl ether), N-terminally modified derivatives including substituted amides such as alkylamides and hydrazides.

[00248] In some cases, one or more L-amino acids in a Peptide is replaced with a D-amino acid.

[00249] In some cases, a Peptide is a retroinverso analog. Sela and Zisman (1997) FASEB

J. 11 :449. Retro-inverso peptide analogs are isomers of linear peptides in which the direction of the amino acid sequence is reversed (retro) and the chirality, D- or L-, of one or more amino acids therein is inverted (inverso), e.g., using D-amino acids rather than L-amino acids. See, e.g., Jameson et al. (1994) Nature 368:744; and Brady et al. (1994) Nature 368:692.

[00250] A Peptide can include a "Protein Transduction Domain" (PTD), which refers to a polypeptide, polynucleotide, carbohydrate, or organic or inorganic compound that facilitates traversing a lipid bilayer, micelle, cell membrane, organelle membrane, or vesicle membrane. A PTD attached to another molecule facilitates the molecule traversing a membrane, for example going from extracellular space to intracellular space, or cytosol to within an organelle. In some embodiments, a PTD is covalently linked to the amino terminus of a Peptide. In some embodiments, a PTD is covalently linked to the carboxyl terminus of a Peptide. Exemplary protein transduction domains include, but are not limited to, a minimal undecapeptide protein transduction domain (corresponding to residues 47-57 of HIV- 1 TAT comprising

YGRKKR QR R; SEQ ID NO: 46); a polyarginine sequence comprising a number of arginines sufficient to direct entry into a cell (e.g., 3, 4, 5, 6, 7, 8, 9, 10, or 10-50 arginines); a VP22 domain (Zender et al. (2002) Cancer Gene Ther. 9(6):489-96); an Drosophila Antennapedia protein transduction domain (Noguchi et al. (2003) Diabetes 52(7): 1732-1737); a truncated human calcitonin peptide (Trehin et al. (2004) Pharm. Research 21 : 1248-1256); polylysine (Wender et al. (2000) Proc. Natl. Acad. Sci. USA 97: 13003-13008); RRQRRTSKLMKR (SEQ ID NO: 47); Transportan GWTLNSAGYLLGKTNLKALAALAKKIL (SEQ ID NO: 48);

KALAWEAKLAKALAKALAKHLAKALAKALKCEA (SEQ ID NO: 49); and

RQIKIWFQNRRMKWK (SEQ ID NO: 50). Exemplary PTDs include, but are not limited to, YGRKKRRQRRR (SEQ ID NO: 46), RKKRRQRRR (SEQ ID NO: 51); an arginine

homopolymer of from 3 arginine residues to 50 arginine residues; Exemplary PTD domain amino acid sequences include, but are not limited to, any of the following: YGRKKRRQRRR (SEQ ID NO: 46); RKKRRQRR (SEQ ID NO: 52); YARAAARQARA (SEQ ID NO: 53);

THRLPRRRRRR (SEQ ID NO: 54); and GGRRARRRRRR (SEQ ID NO: 55).

[00251] The carboxyl group COR ₃ of the amino acid at the C-terminal end of a Peptide can be present in a free form (R3 = OH) or in the form of a physiologically-tolerated alkaline or alkaline earth salt such as, e.g., a sodium, potassium or calcium salt. The carboxyl group can also be esterified with primary, secondary or tertiary alcohols such as, e.g., methanol, branched or unbranched Ci-C ₆ -alkyl alcohols, e.g., ethyl alcohol or tert-butanol. The carboxyl group can also be amidated with primary or secondary amines such as ammonia, branched or unbranched Ci-C ₆ - alkylamines or Ci-C ₆ di-alkylamines, e.g., methylamine or dimethylamine.

[00252] The amino group of the amino acid NRiR ₂ at the N-terminus of a Peptide can be present in a free form (Ri = H and R ₂ = H) or in the form of a physiologically-tolerated salt such as, e.g., a chloride or acetate. The amino group can also be acetylated with acids such that Ri = H and R ₂ = acetyl, trifluoroacetyl, or adamantyl. The amino group can be present in a form protected by amino-protecting groups conventionally used in peptide chemistry such as, e.g., Fmoc, Benzyloxy-carbonyl (Z), Boc, or Alloc. The amino group can be N-alkylated in which Ri and/or R ₂ = Ci-C ₆ alkyl or C ₂ -C8 alkenyl or C7-C9 aralkyl. Alkyl residues can be straight- chained, branched or cyclic (e.g., ethyl, isopropyl and cyclohexyl, respectively).

[00253] A Peptide can include one or more modifications that enhance a property desirable in a protein formulated for therapy (e.g., serum half-life), that enable the raising of antibodies for use in detection assays (e.g., epitope tags), that provide for ease of protein purification, etc. Such modifications include, but are not limited to, pegylation (covalent attachment of one or more molecules of polyethylene glycol (PEG), or derivatives thereof); N- glycosylation and polysialylation; albumin fusion; albumin binding through a conjugated fatty acid chain (acylation); Fc-fusion proteins; and fusion with a PEG mimetic.

[00254] Pegylation: The clinical effectiveness of protein therapeutics is often limited by short plasma half-life and susceptibility to protease degradation. Studies of various therapeutic proteins (e.g., filgrastim) have shown that such difficulties may be overcome by various modifications, including conjugating or linking the polypeptide sequence to any of a variety of non-proteinaceous polymers, e.g., polyethylene glycol (PEG), polypropylene glycol, or polyoxyalkylenes (e.g., typically via a linking moiety covalently bound to both the protein and the non-proteinaceous polymer, e.g., a PEG). Such PEG-conjugated biomolecules have been shown to possess clinically useful properties, including better physical and thermal stability, protection against susceptibility to enzymatic degradation, increased solubility, longer in vivo circulating half-life and decreased clearance, reduced immunogenicity and antigenicity, and reduced toxicity.

[00255] PEGs suitable for conjugation to a polypeptide sequence are generally soluble in water at room temperature, and have the general formula R(0-CH ₂ -CH ₂ )nO-R, where R is hydrogen or a protective group such as an alkyl or an alkanol group, and where n is an integer from 1 to 1000. When R is a protective group, it generally has from 1 to 8 carbons. The PEG conjugated to the polypeptide sequence can be linear or branched. Branched PEG derivatives, "star-PEGs" and multi-armed PEGs are contemplated by the present disclosure. The molecular weight of a PEG used in the present disclosure is not restricted to any particular range, but certain embodiments have a molecular weight between 500 and 20,000, while other

embodiments have a molecular weight between 4,000 and 10,000.

[00256] The present disclosure also contemplates compositions of conjugates wherein the

PEGs have different n values and thus the various different PEGs are present in specific ratios. For example, some compositions comprise a mixture of conjugates where n=l, 2, 3 and 4. In some compositions, the percentage of conjugates where n=l is 18-25%, the percentage of conjugates where n=2 is 50-66%, the percentage of conjugates where n=3 is 12-16%), and the percentage of conjugates where n=4 is up to 5%>. Such compositions can be produced by reaction conditions and purification methods know in the art. For example, cation exchange chromatography may be used to separate conjugates, and a fraction is then identified which contains the conjugate having, for example, the desired number of PEGs attached, purified free from unmodified protein sequences and from conjugates having other numbers of PEGs attached.

[00257] PEG may be bound to a polypeptide of the present disclosure via a terminal reactive group (a "spacer"). The spacer is, for example, a terminal reactive group which mediates a bond between the free amino or carboxyl groups of one or more of the polypeptide sequences and polyethylene glycol. An example of a PEG molecule, modified to include a spacer, that may be bound to the free amino group of a polypeptide is N-hydroxysuccinylimide polyethylene glycol, which may be prepared by activating succinic acid ester of polyethylene glycol with N-hydroxysuccinylimide. Another activated polyethylene glycol which may be bound to a free amino group is 2,4-bis(0-methoxypolyethyleneglycol)-6-chloro-s-triazine, which may be prepared by reacting polyethylene glycol monomethyl ether with cyanuric chloride. Examples of an activated polyethylene glycol bound to the free carboxyl group of a polypeptide include polyoxyethylenediamine.

[00258] Conjugation of one or more of the polypeptide sequences of the present disclosure to PEG having a spacer may be carried out by various conventional methods. For example, the conjugation reaction can be carried out in solution at a pH of from 5 to 10, at a temperature from 4°C to room temperature, for 30 minutes to 20 hours, utilizing a molar ratio of reagent to protein of from 4: 1 to 30: 1. Reaction conditions may be selected to direct the reaction towards producing predominantly a desired degree of substitution. In general, low temperature, low pH (e.g., pH=5), and short reaction time tend to decrease the number of PEGs attached, whereas high temperature, neutral to high pH (e.g., pH>7), and longer reaction time tend to increase the number of PEGs attached. Various means known in the art may be used to terminate the reaction. In some embodiments the reaction is terminated by acidifying the reaction mixture and freezing at, e.g., -20°C.

[00259] The present disclosure also contemplates the use of PEG Mimetics. Recombinant PEG mimetics have been developed that retain the attributes of PEG (e.g., enhanced serum half- life) while conferring several additional advantageous properties. By way of example, simple polypeptide chains (comprising, for example, Ala, Glu, Gly, Pro, Ser and Thr) capable of forming an extended conformation similar to PEG can be produced recombinantly already fused to the peptide or protein of interest (e.g., Amunix' XTEN technology; Mountain View, CA). This obviates the need for an additional conjugation step during the manufacturing process. Moreover, established molecular biology techniques enable control of the side chain composition of the polypeptide chains, allowing optimization of immunogenicity and manufacturing properties.

[00260] Glycosylation and Polysialylation: For purposes of the present disclosure,

"glycosylation" is meant to broadly refer to the enzymatic process that attaches glycans to proteins, lipids or other organic molecules. The use of the term "glycosylation" in conjunction with the present disclosure is generally intended to mean adding or deleting one or more carbohydrate moieties (either by removing the underlying glycosylation site or by deleting the glycosylation by chemical and/or enzymatic means), and/or adding one or more glycosylation sites to the native sequence. In addition, the term includes qualitative changes in the

glycosylation pattern of the native sequence involving a change in the nature and proportions of the various carbohydrate moieties present.

[00261] Glycosylation can dramatically affect the physical properties of proteins and can also be important in protein stability, secretion, and subcellular localization. Proper

glycosylation can be essential for biological activity. In fact, some genes from eucaryotic organisms, when expressed in bacteria (e.g., E. coli) which lack cellular processes for glycosylating proteins, yield proteins that are recovered with little or no activity by virtue of their lack of glycosylation.

[00262] The addition of glycosylation sites can be accomplished by altering the amino acid sequence. The alteration to the polypeptide may be made by, for example, the addition of, or substitution by, one or more serine or threonine residues (for O-linked glycosylation sites) or asparagine residues (for N-linked glycosylation sites). The structures of N-linked and O-linked oligosaccharides and the sugar residues found in each type may be different. One type of sugar that is commonly found in both is N-acetylneuraminic acid (hereafter referred to as sialic acid). Sialic acid is usually the terminal residue of both N-linked and O-linked oligosaccharides and, by virtue of its negative charge, may confer acidic properties to the glycoprotein. A particular embodiment of the present disclosure comprises the generation and use of N-glycosylation variants.

[00263] The polypeptide sequences of the present disclosure may optionally be altered through changes at the DNA level, particularly by mutating the DNA encoding the polypeptide at preselected bases such that codons are generated that will translate into the desired amino acids. Another means of increasing the number of carbohydrate moieties on the polypeptide is by chemical or enzymatic coupling of glycosides to the polypeptide. Removal of carbohydrates may be accomplished chemically or enzymatically, or by substitution of codons encoding amino acid residues that are glycosylated. Chemical deglycosylation techniques are known, and enzymatic cleavage of carbohydrate moieties on polypeptides can be achieved by the use of a variety of endo- and exo-glycosidases.

[00264] Dihydrofolate reductase (DHFR) - deficient Chinese Hamster Ovary (CHO) cells are a commonly used host cell for the production of recombinant glycoproteins. These cells do not express the enzyme beta-galactoside alpha-2,6-sialyltransferase, and therefore do not add sialic acid in the alpha-2,6 linkage to N-linked oligosaccharides of glycoproteins produced in these cells.

[00265] The present disclosure also contemplates the use of polysialylation, the conjugation of peptides and proteins to the naturally occurring, biodegradable a-(2→8) linked polysialic acid ("PSA") in order to improve their stability and in vivo pharmacokinetics. PSA is a biodegradable, non-toxic natural polymer that is highly hydrophilic, giving it a high apparent molecular weight in the blood which increases its serum half-life. In addition, polysialylation of a range of peptide and protein therapeutics has led to markedly reduced proteolysis, retention of in vivo activity, and reduction of immunogenicity and antigenicity (see, e.g., G. Gregoriadis et al, Int. J. Pharmaceutics 300(1-2): 125-30 (2005)). As with modifications with other conjugates (e.g., PEG), various techniques for site-specific polysialylation are available (see, e.g., T.

Lindhout et al, PNAS 108(18)7397-7402 (2011)).

[00266] Albumin Fusion and Conjugation with Other Molecules: Additional suitable components and molecules for conjugation include, for example, thyroglobulin; albumins such as human serum albumin (HAS); tetanus toxoid; Diphtheria toxoid; polyamino acids such as poly(D-lysine:D-glutamic acid); VP6 polypeptides of rotaviruses; influenza virus hemaglutinin, influenza virus nucleoprotein; Keyhole Limpet Hemocyanin (KLH); and hepatitis B virus core protein and surface antigen; or any combination of the foregoing.

[00267] Fusion of albumin to one or more polypeptides of the present disclosure can, for example, be achieved by genetic manipulation, such that the DNA coding for HSA, or a fragment thereof, is joined to the DNA coding for the one or more polypeptide sequences.

Thereafter, a suitable host can be transformed or transfected with the fused nucleotide sequences in the form of, for example, a suitable plasmid, so as to express a fusion polypeptide. The expression may be effected in vitro from, for example, prokaryotic or eukaryotic cells, or in vivo from, for example, a transgenic organism. In some embodiments of the present disclosure, the expression of the fusion protein is performed in mammalian cell lines, for example, CHO cell lines. Transformation is used broadly herein to refer to the genetic alteration of a cell resulting from the direct uptake, incorporation and expression of exogenous genetic material (exogenous DNA) from its surroundings and taken up through the cell membrane(s). Transformation occurs naturally in some species of bacteria, but it can also be effected by artificial means in other cells.

[00268] Furthermore, albumin itself may be modified to extend its circulating half-life.

Fusion of the modified albumin to one or more Peptides can be attained by the genetic manipulation techniques described above or by chemical conjugation; the resulting fusion molecule has a half-life that exceeds that of fusions with un-modified albumin. (See, e.g., WO2011/051489).

[00269] Several albumin - binding strategies have been developed as alternatives to direct fusion, including albumin binding through a conjugated fatty acid chain (acylation). Because serum albumin is a transport protein for fatty acids, these natural ligands with albumin-binding activity have been used for half-life extension of small protein therapeutics. For example, insulin determir (LEVEMIR), an approved product for diabetes, comprises a myristyl chain conjugated to a genetically-modified insulin, resulting in a long-acting insulin analog.

[00270] Another type of modification involves conjugation of one or more additional components or molecules at the N- and/or C-terminus of a polypeptide sequence, such as another protein (e.g., a protein having an amino acid sequence heterologous to the subject protein), or a carrier molecule. Thus, an exemplary polypeptide sequence can be provided as a conjugate with another component or molecule.

[00271] A conjugate modification may result in a polypeptide sequence that retains its inherent activity but also has an additional or complementary function or activity of the second molecule. For example, a polypeptide sequence may be conjugated to a molecule to, e.g., facilitate solubility, storage, in vivo or shelf half-life or stability, reduction in immunogenicity, delayed or controlled release in vivo, etc. Other functions or activities include a conjugate that reduces toxicity relative to an unconjugated polypeptide sequence, a conjugate that targets a type of cell or organ more efficiently than an unconjugated polypeptide sequence, or a drug to further counter the causes or effects associated with a disorder or disease as set forth herein (e.g., diabetes).

[00272] A polypeptide may also be conjugated to large, slowly metabolized

macromolecules such as proteins; polysaccharides, such as sepharose, agarose, cellulose and cellulose beads; polymeric amino acids such as polyglutamic acid and polylysine; amino acid copolymers; inactivated virus particles; inactivated bacterial toxins such as toxoid from diphtheria, tetanus, cholera and leukotoxin molecules; inactivated bacteria; and dendritic cells. If desired, such conjugated forms can be used to produce antibodies against a polypeptide of the present disclosure.

[00273] Additional candidate components and molecules for conjugation include those suitable for isolation or purification. Particular non-limiting examples include binding molecules, such as biotin (biotin-avidin - specific binding pair), an antibody, a receptor, a ligand, a lectin, or molecules that comprise a solid support, including, for example, plastic or

polystyrene beads, plates or beads, magnetic beads, test strips, and membranes.

[00274] Purification methods such as cation exchange chromatography may be used to separate conjugates by charge difference, which effectively separates conjugates into their various molecular weights. For example, a cation exchange column can be loaded and then washed with -20 mM sodium acetate, pH -4, and then eluted with a linear (0 M to 0.5 M) NaCl gradient buffered at a pH from about 3 to 5.5, e.g., at pH -4.5. The content of the fractions obtained by cation exchange chromatography may be identified by molecular weight using conventional methods, for example, mass spectroscopy, SDS-PAGE, or other known methods for separating molecular entities by molecular weight.

[00275] Fc-fusion Molecules: In certain embodiments, the amino- or carboxyl- terminus of a polypeptide sequence of the present disclosure can be fused with an immunoglobulin Fc region (e.g., human Fc) to form a fusion conjugate (or fusion molecule). Fc fusion conjugates have been shown to increase the systemic half-life of biopharmaceuticals, and thus the biopharmaceutical product may require less frequent administration.

[00276] Fc binds to the neonatal Fc receptor (FcRn) in endothelial cells that line the blood vessels, and, upon binding, the Fc fusion molecule is protected from degradation and re-released into the circulation, keeping the molecule in circulation longer. This Fc binding is believed to be the mechanism by which endogenous IgG retains its long plasma half-life. More recent Fc- fusion technology links a single copy of a biopharmaceutical to the Fc region of an antibody to optimize the pharmacokinetic and pharmacodynamic properties of the biopharmaceutical as compared to traditional Fc-fusion conjugates.

[00277] Other Modifications: The present disclosure contemplates the use of other modifications, currently known or developed in the future, of polypeptides to improve one or more properties. One such method for prolonging the circulation half-life, increasing the stability, reducing the clearance, or altering the immunogenicity or allergenicity of a polypeptide of the present disclosure involves modification of the polypeptide sequences by hesylation, which utilizes hydroxyethyl starch derivatives linked to other molecules in order to modify the molecule's characteristics. Various aspects of hesylation are described in, for example, U.S. Patent Appln. Nos. 2007/0134197 and 2006/0258607.

[00278] Any of the foregoing components and molecules used to modify the polypeptide sequences of the present disclosure may optionally be conjugated via a linker. Suitable linkers include "flexible linkers" which are generally of sufficient length to permit some movement between the modified polypeptide sequences and the linked components and molecules. The linker molecules are generally about 6-50 atoms long. The linker molecules may also be, for example, aryl acetylene, ethylene glycol oligomers containing 2-10 monomer units, diamines, diacids, amino acids, or combinations thereof. Suitable linkers can readily be selected and can be of any suitable length, such as 1 (e.g., Gly), 2, 3, 4, 5, 6, 7, 8, 9, 10, 10-20, 20-30, 30-50 amino acids (e.g., Gly).

[00279] Exemplary flexible linkers include glycine polymers (G) _n , glycine-serine polymers (for example, (GS)„, GSGGS _n (SEQ ID NO: 69) and GGGS„ (SEQ ID NO: 70), where n is an integer of at least one), glycine-alanine polymers, alanine-serine polymers, and other flexible linkers. Glycine and glycine-serine polymers are relatively unstructured, and therefore may serve as a neutral tether between components. Exemplary flexible linkers include, but are not limited to, GGSG (SEQ ID NO: 71), GGSGG (SEQ ID NO: 72), GSGSG (SEQ ID NO: 73), GSGGG (SEQ ID NO: 74), GGGSG (SEQ ID NO: 75), and GSSSG (SEQ ID NO: 76).

METHODS OF PRODUCTION OF PEPTIDES

[00280] A peptide of the present disclosure (e.g., an Ednl Peptide; a Habp2 Peptide; a Kazaldl Peptide; a Respl8 Peptide; or a Tinag Peptide) can be produced by any suitable method, including recombinant and non-recombinant methods (e.g., chemical synthesis).

A. Chemical Synthesis

[00281] Where a polypeptide is chemically synthesized, the synthesis may proceed via liquid-phase or solid-phase. Solid-phase peptide synthesis (SPPS) allows the incorporation of unnatural amino acids and/or peptide/protein backbone modification. Various forms of SPPS, such as Fmoc and Boc, are available for synthesizing peptides of the present disclosure. Details of the chemical synthesis are known in the art (e.g., Ganesan A. 2006 Mini Rev. Med Chem. 6:3- 10 and Camarero JA et al. 2005 Protein Pept Lett. 12:723-8).

[00282] Solid phase peptide synthesis may be performed as described hereafter. The a functions (Na) and any reactive side chains are protected with acid-labile or base-labile groups. The protective groups are stable under the conditions for linking amide bonds but can be readily cleaved without impairing the peptide chain that has formed. Suitable protective groups for the a-amino function include, but are not limited to, the following: t-butyloxycarbonyl (Boc), benzyloxycarbonyl (Z), o-chlorbenzyloxycarbonyl, bi-phenylisopropyloxycarbonyl, tert- amyloxycarbonyl (Amoc), a, a-dimethyl-3,5-dimethoxy-benzyloxycarbonyl, o-nitrosulfenyl, 2- cyano-t-butoxy-carbonyl, 9-fluorenylmethoxycarbonyl (Fmoc), l-(4,4-dimethyl-2,6- dioxocylohex-l-ylidene)ethyl (Dde) and the like. For example, 9-fluorenylmethoxycarbonyl (Fmoc) can be used as the Na-protective group.

[00283] Suitable side chain protective groups include, but are not limited to: acetyl, allyl

(All), allyloxycarbonyl (Alloc), benzyl (Bzl), benzyloxycarbonyl (Z), t-butyloxycarbonyl (Boc), benzyloxymethyl (Bom), o-bromobenzyloxycarbonyl, t-butyl (tBu), t-butyldimethylsilyl, 2- chlorobenzyl, 2-chlorobenzyloxycarbonyl (2-CIZ), 2,6-dichlorobenzyl, cyclohexyl, cyclopentyl, l-(4,4-dimethyl-2,6-dioxocyclohex-l-ylidene)ethyl (Dde), isopropyl, 4-methoxy-2,3-6- trimethylbenzylsulfonyl (Mtr), 2,3,5,7,8-pentamethylchroman-6-sulfonyl (Pmc), pivalyl, tetrahydropyran-2-yl, tosyl (Tos), 2,4,6-trimethoxybenzyl, trimethylsilyl and trityl (Trt).

[00284] In the solid phase synthesis, the C-terminal amino acid is coupled to a suitable support material. Suitable support materials are those which are inert towards the reagents and reaction conditions for the step-wise condensation and cleavage reactions of the synthesis process and which do not dissolve in the reaction media being used. Examples of commercially- available support materials include styrene/divinylbenzene copolymers which have been modified with reactive groups and/or polyethylene glycol; chloromethylated

styrene/divinylbenzene copolymers; hydroxymethylated or aminomethylated

styrene/divinylbenzene copolymers and the like. Polystyrene (l%)-divinylbenzene or TentaGel® derivatized with 4-benzyloxybenzyl-alcohol (Wang-anchor) or 2-chlorotrityl chloride can be used if it is intended to prepare the peptidic acid. In the case of the peptide amide, polystyrene (1%) divinylbenzene or TentaGel® derivatized with 5-(4'-aminomethyl)-3',5'- dimethoxyphenoxy)valeric acid (PAL-anchor) or p-(2,4-dimethoxyphenyl-amino methyl)- phenoxy group (Rink amide anchor) can be used.

[00285] The linkage to the polymeric support can be achieved by reacting the C-terminal

Fmoc-protected amino acid with the support material with the addition of an activation reagent in ethanol, acetonitrile, Ν,Ν-dimethylformamide (DMF), dichloromethane, tetrahydrofuran, N- methylpyrrolidone or similar solvents at room temperature or elevated temperatures (e.g., between 40°C and 60°C) and with reaction times of, e.g., 2 to 72 hours.

[00286] The coupling of the Na-protected amino acid (e.g., the Fmoc amino acid) to the

PAL, Wang or Rink anchor can, for example, be carried out with the aid of coupling reagents such as Ν,Ν'-dicyclohexylcarbodiimide (DCC), Ν,Ν'-diisopropylcarbodiimide (DIC) or other carbodiimides, 2-(lH-benzotriazol-l-yl)-l,l,3,3-tetramethyluronium tetrafluoroborate (TBTU) or other uronium salts, o-acyl-ureas, benzotriazol-l-yl-tris-pyrrolidino-phosphonium hexafluorophosphate (PyBOP) or other phosphonium salts, N-hydroxysuccinimides, other N- hydroxyimides or oximes in the presence or also in the absence of 1-hydroxybenzotriazole or 1- hydroxy-7-azabenzotriazole, e.g., with the aid of TBTU with addition of HOBt, with or without the addition of a base such as for example diisopropylethylamine (DIEA), triethylamine or N- methylmorpholine, e.g., diisopropylethylamine with reaction times of 2 to 72 hours (e.g., 3 hours in a 1.5 to 3-fold excess of the amino acid and the coupling reagents, e.g., in a 2-fold excess and at temperatures between about 10°C and 50°C, e.g., 25°C in a solvent such as

dimethylformamide, N-methylpyrrolidone or dichloromethane, e.g., dimethylformamide).

[00287] Instead of the coupling reagents, it is also possible to use the active esters (e.g., pentafluorophenyl, p-nitrophenyl or the like), the symmetric anhydride of the Na-Fmoc-amino acid, its acid chloride or acid fluoride under the conditions described above.

[00288] The Na-protected amino acid (e.g., the Fmoc amino acid) can be coupled to the 2- chlorotrityl resin in dichloromethane with the addition of DIEA with reaction times of 10 to 120 minutes, e.g., 20 minutes, but is not limited to the use of this solvent and this base.

[00289] The successive coupling of the protected amino acids can be carried out according to conventional methods in peptide synthesis, typically in an automated peptide synthesizer. After cleavage of the Na-Fmoc protective group of the coupled amino acid on the solid phase by treatment with, e.g., piperidine (10% to 50%>) in dimethylformamide for 5 to 20 minutes, e.g., 2 x 2 minutes with 50%> piperidine in DMF and 1 x 15 minutes with 20%> piperidine in DMF, the next protected amino acid in a 3 to 10-fold excess, e.g., in a 10-fold excess, is coupled to the previous amino acid in an inert, non-aqueous, polar solvent such as dichloromethane, DMF or mixtures of the two and at temperatures between about 10°C and 50°C, e.g., at 25°C. The previously mentioned reagents for coupling the first Na-Fmoc amino acid to the PAL, Wang or Rink anchor are suitable as coupling reagents. Active esters of the protected amino acid, or chlorides or fluorides or symmetric anhydrides thereof can also be used as an alternative.

[00290] At the end of the solid phase synthesis the peptide is cleaved from the support material while simultaneously cleaving the side chain protecting groups. Cleavage can be carried out with trifluoroacetic acid or other strongly acidic media with addition of 5%-20% V/V of scavengers such as dimethylsulfide, ethylmethylsulfide, thioanisole, thiocresol, m-cresol, anisole ethanedithiol, phenol or water, e.g., 15%> v/v dimethylsulfide/ethanedithiol/m-cresol 1 : 1 : 1, within 0.5 to 3 hours, e.g., 2 hours. Peptides with fully protected side chains are obtained by cleaving the 2-chlorotrityl anchor with glacial acetic acid/trifluoroethanol/dichloromethane 2:2:6. The protected peptide can be purified by chromatography on silica gel. If the peptide is linked to the solid phase via the Wang anchor and if it is intended to obtain a peptide with a C-terminal alkylamidation, the cleavage can be carried out by aminolysis with an alkylamine or

fluoroalkylamine. The aminolysis is carried out at temperatures between about -10°C and 50°C, e.g., about 25°C and reaction times between about 12 and 24 hours, e.g., about 18 hours. In addition the peptide can also be cleaved from the support by re-esterification, e.g., with methanol.

[00291] The acidic solution that is obtained may be admixed with a 3 to 20-fold amount of cold ether or n-hexane, e.g., a 10-fold excess of diethyl ether, in order to precipitate the peptide and hence to separate the scavengers and cleaved protective groups that remain in the ether. A further purification can be carried out by re -precipitating the peptide several times from glacial acetic acid. The precipitate that is obtained can be taken up in water or tert- butanol or mixtures of the two solvents, e.g., a 1 : 1 mixture of tert-butanol/water, and freeze-dried.

[00292] The peptide obtained can be purified by various chromatographic methods, including ion exchange over a weakly basic resin in the acetate form; hydrophobic adsorption chromatography on non-derivatized polystyrene/divinylbenzene copolymers (e.g., Amberlite® XAD); adsorption chromatography on silica gel; ion exchange chromatography, e.g., on carboxymethyl cellulose; distribution chromatography, e.g., on Sephadex® G-25; countercurrent distribution chromatography; or high pressure liquid chromatography (HPLC) e.g., reversed- phase HPLC on octyl or octadecylsilylsilica (ODS) phases.

B. Recombinant Production

[00293] Where a peptide is produced using recombinant techniques, the peptide may be produced as an intracellular protein or as a secreted protein, using any suitable construct and any suitable host cell, which can be a prokaryotic or eukaryotic cell, such as a bacterial (e.g., E. coli) or a yeast host cell, respectively. Other examples of eukaryotic cells that may be used as host cells include insect cells, mammalian cells, and/or plant cells. Where mammalian host cells are used, they may include human cells (e.g., HeLa, 293, H9 and Jurkat cells); mouse cells (e.g., NIH3T3, L cells, and C127 cells); primate cells (e.g., Cos 1, Cos 7 and CV1) and hamster cells (e.g., Chinese hamster ovary (CHO) cells).

[00294] A variety of host- vector systems suitable for the expression of a peptide may be employed according to standard procedures known in the art. See, e.g., Sambrook et al, 1989 Current Protocols in Molecular Biology Cold Spring Harbor Press, New York and Ausubel et al. 1995 Current Protocols in Molecular Biology, Eds. Wiley and Sons. Methods for introduction of genetic material into host cells include, for example, transformation, electroporation,

conjugation, calcium phosphate methods and the like. The method for transfer can be selected so as to provide for stable expression of the introduced polypeptide-encoding nucleic acid. The polypeptide-encoding nucleic acid can be provided as an inheritable episomal element (e.g., a plasmid) or can be genomically integrated. A variety of appropriate vectors for use in production of a peptide of interest are available commercially.

[00295] Vectors can provide for extrachromosomal maintenance in a host cell or can provide for integration into the host cell genome. The expression vector provides transcriptional and translational regulatory sequences, and may provide for inducible or constitutive expression where the coding region is operably-linked under the transcriptional control of the transcriptional initiation region, and a transcriptional and translational termination region. In general, the transcriptional and translational regulatory sequences may include, but are not limited to, promoter sequences, ribosomal binding sites, transcriptional start and stop sequences, translational start and stop sequences, and enhancer or activator sequences. Promoters can be either constitutive or inducible, and can be a strong constitutive promoter (e.g., T7, and the like).

[00296] Expression constructs generally have convenient restriction sites located near the promoter sequence to provide for the insertion of nucleic acid sequences encoding proteins of interest. A selectable marker operative in the expression host may be present to facilitate selection of cells containing the vector. In addition, the expression construct may include additional elements. For example, the expression vector may have one or two replication systems, thus allowing it to be maintained in organisms, for example, in mammalian or insect cells for expression and in a prokaryotic host for cloning and amplification. In addition, the expression construct may contain a selectable marker gene to allow the selection of transformed host cells. Selectable genes are well known in the art and will vary with the host cell used. [00297] Isolation and purification of a protein can be accomplished according to methods known in the art. For example, a protein can be isolated from a lysate of cells genetically modified to express the protein constitutively and/or upon induction, or from a synthetic reaction mixture by immunoaffinity purification, which generally involves contacting the sample with an anti- protein antibody, washing to remove non-specifically bound material, and eluting the specifically bound protein. The isolated protein can be further purified by dialysis and other methods normally employed in protein purification methods. In one embodiment, the protein may be isolated using metal chelate chromatography methods. Proteins may contain

modifications to facilitate isolation.

[00298] The peptides may be prepared in substantially pure or isolated form (e.g., free from other polypeptides). The peptides can present in a composition that is enriched for the peptide relative to other components that may be present (e.g., other polypeptides or other host cell components). Purified peptide may be provided such that the peptide is present in a composition that is substantially free of other expressed proteins, e.g., less than 90%, less than 60%, less than 50%, less than 40%, less than 30%, less than 20%, less than 10%, less than 5%, or less than 1%, of the composition is made up of other expressed proteins.

ANTIBODIES

[00299] The term "antibody" encompasses intact monoclonal antibodies, polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies) formed from at least two intact antibodies, and antibody binding fragments including Fab and F(ab)' ₂ , provided that they exhibit the desired biological activity. The basic antibody structural unit comprises a tetramer, and each tetramer is composed of two identical pairs of polypeptide chains, each pair having one "light" chain (about 25 kDa) and one "heavy" chain (about 50-70 kDa). The amino-terminal portion of each chain includes a variable region of about 100 to 110 or more amino acids primarily responsible for antigen recognition. In contrast, the carboxy-terminal portion of each chain defines a constant region primarily responsible for effector function. Human light chains are classified as kappa and lambda light chains, whereas human heavy chains are classified as mu, delta, gamma, alpha, or epsilon, and define the antibody's isotype as IgM, IgD, IgA, and IgE, respectively. Binding fragments are produced by recombinant DNA techniques, or by enzymatic or chemical cleavage of intact antibodies. Binding fragments include Fab, Fab', F(ab') ₂ , Fv, and single-chain antibodies.

[00300] Each heavy chain has at one end a variable domain (VH) followed by a number of constant domains. Each light chain has a variable domain at one end (VL) and a constant domain at its other end; the constant domain of the light chain is aligned with the first constant domain of the heavy chain, and the light chain variable domain is aligned with the variable domain of the heavy chain. Within light and heavy chains, the variable and constant regions are joined by a "J" region of about 12 or more amino acids, with the heavy chain also including a "D" region of about 10 more amino acids. The antibody chains all exhibit the same general structure of relatively conserved framework regions (FR) joined by three hyper-variable regions, also called complementarity-determining regions or CDRs. The CDRs from the two chains of each pair are aligned by the framework regions, enabling binding to a specific epitope. From N- terminal to C-terminal, both light and heavy chains comprise the domains FR1, CDR1, FR2, CDR2, FR3, CDR3 and FR4.

[00301] An intact antibody has two binding sites and, except in bifunctional or bispecific antibodies, the two binding sites are the same. A bispecific or bifunctional antibody is an artificial hybrid antibody having two different heavy/light chain pairs and two different binding sites. Bispecific antibodies can be produced by a variety of methods including fusion of hybridomas or linking of Fab' fragments.

[00302] As set forth above, binding fragments may be produced by enzymatic or chemical cleavage of intact antibodies. Digestion of antibodies with the enzyme papain results in two identical antigen-binding fragments, also known as "Fab" fragments, and an "Fc" fragment which has no antigen-binding activity. Digestion of antibodies with the enzyme pepsin results in a F(ab')2 fragment in which the two arms of the antibody molecule remain linked and comprise two-antigen binding sites. The F(ab')2 fragment has the ability to crosslink antigen.

[00303] As used herein the term "Fab" refers to a fragment of an antibody that comprises the constant domain of the light chain and the CHI domain of the heavy chain.

[00304] The term "Fv" when used herein refers to the minimum fragment of an antibody that retains both antigen-recognition and antigen-binding sites. In a two-chain Fv species, this region includes a dimer of one heavy-chain and one light-chain variable domain in non-covalent association. In a single-chain Fv species, one heavy-chain and one light-chain variable domain can be covalently linked by a flexible peptide linker such that the light and heavy chains can associate in a "dimeric" structure analogous to that in a two-chain Fv species. It is in this configuration that the three CDRs of each variable domain interact to define an antigen-binding site on the surface of the VH-VL dimer. While the six CDRs, collectively, confer antigen- binding specificity to the antibody, even a single variable domain (or half of an Fv comprising only three CDRs specific for an antigen) has the ability to recognize and bind antigen.

[00305] When used herein, the term "complementarity determining regions" or "CDRs" refers to parts of immunological receptors that make contact with a specific ligand and determine its specificity.

[00306] The term "hypervariable region" refers to the amino acid residues of an antibody which are responsible for antigen-binding. The hypervariable region generally comprises amino acid residues from a "complementarity determining region" or "CDR" and/or those residues from a "hypervariable loop".

[00307] As used herein, the term "epitope" refers to binding sites for antibodies on protein antigens. Epitopic determinants usually comprise chemically active surface groupings of molecules such as amino acids or sugar side chains, as well as specific three dimensional structural and charge characteristics. An antibody is said to bind an antigen when the dissociation constant is <1 μΜ, < 100 nM, or < 10 nM. An increased equilibrium constant ("KD") means that there is less affinity between the epitope and the antibody, whereas a decreased equilibrium constant means that there is a higher affinity between the epitope and the antibody. An antibody with a KD of "no more than" a certain amount means that the antibody will bind to the epitope with the given KD or more strongly. Whereas KD describes the binding characteristics of an epitope and an antibody, "potency" describes the effectiveness of the antibody itself for a function of the antibody. There is not necessarily a correlation between an equilibrium constant and potency; thus, for example, a relatively low KD does not automatically mean a high potency.

[00308] The term "selectively binds" in reference to an antibody does not mean that the antibody only binds to a single substance, but rather that the K _D of the antibody to a first substance is less than the KD of the antibody to a second substance. An antibody that exclusively binds to an epitope only binds to that single epitope. [00309] When administered to humans, antibodies that contain rodent (i.e., murine or rat) variable and/or constant regions are sometimes associated with, for example, rapid clearance from the body or the generation of an immune response by the body against the antibody. In order to avoid the utilization of rodent-derived antibodies, fully human antibodies can be generated through the introduction of human antibody function into a rodent so that the rodent produces fully human antibodies. Unless specifically identified herein, "human" and "fully human" antibodies can be used interchangeably herein. The term "fully human" can be useful when distinguishing antibodies that are only partially human from those that are completely, or fully human. The skilled artisan is aware of various methods of generating fully human antibodies.

[00310] In order to address possible human anti-mouse antibody responses, chimeric or otherwise humanized antibodies can be utilized. Chimeric antibodies have a human constant region and a murine variable region, and, as such, human anti-chimeric antibody responses may be observed in some patients. Therefore, it is advantageous to provide fully human antibodies against multimeric enzymes in order to avoid possible human anti-mouse antibody or human anti-chimeric antibody responses.

[00311] Fully human monoclonal antibodies can be prepared, for example, by the generation of hybridoma cell lines by techniques known to the skilled artisan. Other preparation methods involve the use of sequences encoding particular antibodies for transformation of a suitable mammalian host cell, such as a CHO cell. Transformation can be by any known method for introducing polynucleotides into a host cell, including, for example, packaging the

polynucleotide in a virus (or into a viral vector) and transducing a host cell with the virus (or vector) or by transfection procedures known in the art. Methods for introducing heterologous polynucleotides into mammalian cells are well known in the art and include dextran-mediated transfection, calcium phosphate precipitation, polybrene -mediated transfection, protoplast fusion, electroporation, encapsulation of the polynucleotide(s) in liposomes, and direct microinjection of the DNA into nuclei. Mammalian cell lines available as hosts for expression are well known in the art and include, but are not limited to CHO cells, HeLa cells, and human hepatocellular carcinoma cells.

[00312] The antibodies of the present disclosure can be used diagnostically and/or therapeutically. For example, the antibodies can be used as a diagnostic by detecting the level of one or more peptides of the present disclosure in a subject, and either comparing the detected level to a standard control level or to a baseline level in a subject determined previously (e.g., prior to any illness). The antibodies can be used as a therapeutic to modulate the activity of one or more peptides of the present disclosure, thereby having an effect on a condition or disorder associated with the one or more peptides.

[00313] Another embodiment of the present disclosure entails the use of one or more human domain antibodies (dAb). dAbs are the smallest functional binding units of human antibodies (IgGs) and have favorable stability and solubility characteristics. The technology entails a dAb(s) conjugated to HSA (thereby forming a "AlbudAb"; see, e.g., EP1517921B, WO2005/118642 and WO2006/051288) and a molecule of interest (e.g., a peptide of the present disclosure). AlbudAbs are often smaller and easier to manufacture in microbial expression systems, such as bacteria or yeast, than current technologies used for extending the serum half- life of peptides. As HSA has a half-life of about three weeks, the resulting conjugated molecule improves the half-life of the molecule of interest. Use of the dAb technology may also enhance the efficacy of the molecule of interest.

THERAPEUTIC AND PROPHYLACTIC USES

[00314] The present disclosure provides methods for treating or preventing

hyperglycemia, hyperinsulinemia, glucose intolerance, glucose metabolism disorders, obesity, as well as other metabolic and metabolic-associated diseases, disorders and conditions by the administration of the Modulators, or compositions thereof, as described herein. Such methods may also have an advantageous effect on one or more of symptoms associated with a disease, disorder or condition by, for example, decreasing the severity or the frequency of a symptom.

[00315] In order to determine whether a subject may be a candidate for the treatment or prevention of hyperglycemia, hyperinsulinemia, glucose intolerance, and/or glucose disorders by the methods provided herein, various diagnostic methods known in the art may be utilized. Such methods include those described elsewhere herein (e.g., fasting plasma glucose (FPG) evaluation and the oral glucose tolerance test (oGTT)).

[00316] In order to determine whether a subject may be a candidate for the treatment or prevention of obesity by the methods provided herein, parameters such as, but not limited to, the etiology and the extent of the subject's condition (i.e., how overweight the subject is compared to reference healthy individual) should be evaluated. For example, a subject may be considered obese or overweight by assessment of the subject's Body Mass Index (BMI). An adult having a BMI in the range of 18.5 to 24.9 kg/m ² is considered to have a normal weight; an adult having a BMI between 25 and 29.9 kg/m ² may be considered overweight (pre -obese); an adult who has a BMI of 30 kg/m ² or higher may be considered obese. For subjects who are overweight and/or who have poor diets (e.g., diets high in fat and calories), it is common to initially implement and assess the effect of modified dietary habits and/or exercise regimens before initiating a course of therapy comprising one or more of the Modulators of the present disclosure.

PHARMACEUTICAL COMPOSITIONS, ROUTES OF ADMINISTRATION, COMBINATION THERAPY, AND DOSING

[00317] The Modulators of the present disclosure may be in the form of compositions suitable for administration to a subject. In general, such compositions are "pharmaceutical compositions" comprising one or more Modulators and one or more pharmaceutically acceptable or physiologically acceptable diluents, carriers or excipients. In certain embodiments, the Modulators are present in a therapeutically acceptable amount. The pharmaceutical

compositions may be used in the methods of the present disclosure ; thus, for example, the pharmaceutical compositions can be administered ex vivo or in vivo to a subject in order to practice the therapeutic and prophylactic methods and uses described herein.

[00318] The pharmaceutical compositions of the present disclosure can be formulated to be compatible with the intended method or route of administration; exemplary routes of administration are set forth herein. Furthermore, the pharmaceutical compositions may be used in combination with other therapeutically active agents or compounds (e.g., glucose lowering agents) as described herein in order to treat or prevent the diseases, disorders and conditions as contemplated by the present disclosure.

[00319] The pharmaceutical compositions typically comprise a therapeutically effective amount of at least one of the Modulators contemplated by the present disclosure and one or more pharmaceutically and physiologically acceptable formulation agents. Suitable pharmaceutically acceptable or physiologically acceptable diluents, carriers or excipients include, but are not limited to, antioxidants (e.g., ascorbic acid and sodium bisulfate), preservatives (e.g., benzyl alcohol, methyl parabens, ethyl or n-propyl, p-hydroxybenzoate), emulsifying agents, suspending agents, dispersing agents, solvents, fillers, bulking agents, detergents, buffers, vehicles, diluents, and/or adjuvants. For example, a suitable vehicle may be physiological saline solution or citrate buffered saline, possibly supplemented with other materials common in pharmaceutical compositions for parenteral administration. Neutral buffered saline or saline mixed with serum albumin are further exemplary vehicles. Those skilled in the art will readily recognize a variety of buffers that could be used in the pharmaceutical compositions and dosage forms. Typical buffers include, but are not limited to pharmaceutically acceptable weak acids, weak bases, or mixtures thereof. As an example, the buffer components are water soluble materials such as phosphoric acid, tartaric acids, lactic acid, succinic acid, citric acid, acetic acid, ascorbic acid, aspartic acid, glutamic acid, and salts thereof. Acceptable buffering agents include, for example, a Tris buffer, N-(2-Hydroxyethyl)piperazine-N'-(2-ethanesulfonic acid) (HEPES), 2-(N- Morpholino)ethanesulfonic acid (MES), 2-(N-Morpholino)ethanesulfonic acid sodium salt (MES), 3-(N-Morpholino)propanesulfonic acid (MOPS), and N-tris[Hydroxymethyl]methyl-3- aminopropanesulfonic acid (TAPS).

[00320] After a pharmaceutical composition has been formulated, it may be stored in sterile vials as a solution, suspension, gel, emulsion, solid, or dehydrated or lyophilized powder. Such formulations may be stored either in a ready to use form, a lyophilized form requiring reconstitution prior to use, a liquid form requiring dilution prior to use, or other acceptable form. In some embodiments, the pharmaceutical composition is provided in a single-use container (e.g., a single-use vial, ampoule, syringe, or autoinjector (similar to, e.g., an EpiPen®)), whereas a multi-use container (e.g., a multi-use vial) is provided in other embodiments. Any drug delivery apparatus may be used to deliver the Modulators (e.g., Peptides), including implants (e.g., implantable pumps) and catheter systems, both of which are well known to the skilled artisan. Depot injections, which are generally administered subcutaneously or intramuscularly, may also be utilized to release the peptides disclosed herein over a defined period of time. Depot injections are usually either solid- or oil-based and generally comprise at least one of the formulation components set forth herein. One of ordinary skill in the art is familiar with possible formulations and uses of depot injections.

[00321] The pharmaceutical compositions may be in the form of a sterile injectable aqueous or oleagenous suspension. This suspension may be formulated according to the known art using those suitable dispersing or wetting agents and suspending agents been mentioned herein. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally-acceptable diluent or solvent, for example, as a solution in 1,3-butane diol. Acceptable diluents, solvents and dispersion media that may be employed include water, Ringer's solution, isotonic sodium chloride solution, Cremophor EL™ (BASF, Parsippany, NJ) or phosphate buffered saline (PBS), ethanol, polyol (e.g., glycerol, propylene glycol, and liquid polyethylene glycol), and suitable mixtures thereof. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed including synthetic mono- or diglycerides. Moreover, fatty acids such as oleic acid find use in the preparation of injectables. Prolonged absorption of particular injectable formulations can be achieved by including an agent that delays absorption (e.g., aluminum monostearate or gelatin).

[00322] The pharmaceutical compositions containing the active ingredient may be in a form suitable for oral use, for example, as tablets, capsules, troches, lozenges, aqueous or oily suspensions, dispersible powders or granules, emulsions, hard or soft capsules, or syrups, solutions, microbeads or elixirs. Pharmaceutical compositions intended for oral use may be prepared according to any method known to the art for the manufacture of pharmaceutical compositions, and such compositions may contain one or more agents selected from sweetening agents, flavoring agents, coloring agents and preserving agents in order to provide

pharmaceutically elegant and palatable preparations. Tablets contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets. These excipients may be, for example, diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example, corn starch, or alginic acid; binding agents, for example starch, gelatin or acacia, and lubricating agents, for example magnesium stearate, stearic acid or talc.

[00323] The tablets, capsules and the like suitable for oral administration may be uncoated or they may be coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period. For example, a time-delay material such as glyceryl monostearate or glyceryl distearate may be employed. They may also be coated by techniques known in the art to form osmotic therapeutic tablets for controlled release. Additional agents include biodegradable or biocompatible particles or a polymeric substance such as polyesters, polyamine acids, hydrogel, polyvinyl pyrrolidone, polyanhydrides, polyglycolic acid, ethylene -vinylacetate, methylcellulose,

carboxymethylcellulose, protamine sulfate, or lactide/glycolide copolymers,

polylactide/glycolide copolymers, or ethylenevinylacetate copolymers in order to control delivery of an administered composition. For example, the oral agent can be entrapped in microcapsules prepared by coacervation techniques or by interfacial polymerization, by the use of hydroxymethylcellulose or gelatin-microcapsules or poly (methylmethacrolate)

microcapsules, respectively, or in a colloid drug delivery system. Colloidal dispersion systems include macromolecule complexes, nano-capsules, microspheres, microbeads, and lipid-based systems, including oil-in-water emulsions, micelles, mixed micelles, and liposomes. Methods of preparing liposomes are described in, for example, U.S. Patent Nos. 4,235,871, 4,501,728, and 4,837,028. Methods for the preparation of the above-mentioned formulations will be apparent to those skilled in the art and are commercially available.

[00324] Formulations for oral use may also be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate, kaolin or microcrystalline cellulose, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example peanut oil, liquid paraffin, or olive oil.

[00325] Aqueous suspensions contain the active materials in admixture with excipients suitable for the manufacture thereof. Such excipients are suspending agents, for example sodium carboxymethylcellulose, methylcellulose, hydroxy-propylmethylcellulose, sodium alginate, polyvinyl -pyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents may be a naturally-occurring phosphatide, for example lecithin, or condensation products of an alkylene oxide with fatty acids, for example polyoxy-ethylene stearate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol anhydrides, for example polyethylene sorbitan monooleate. The aqueous suspensions may also contain one or more preservatives.

[00326] Oily suspensions may be formulated by suspending the active ingredient in a vegetable oil, for example arachis oil, olive oil, sesame oil or coconut oil, or in a mineral oil such as liquid paraffin. The oily suspensions may contain a thickening agent, for example beeswax, hard paraffin or cetyl alcohol. Sweetening agents such as those set forth above, and flavoring agents may be added to provide a palatable oral preparation.

[00327] Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water provide the active ingredient in admixture with a dispersing or wetting agent, suspending agent and one or more preservatives. Suitable dispersing or wetting agents and suspending agents are exemplified herein.

[00328] The pharmaceutical compositions of the present disclosure may also be in the form of oil-in-water emulsions. The oily phase may be a vegetable oil, for example olive oil or arachis oil, or a mineral oil, for example, liquid paraffin, or mixtures of these. Suitable emulsifying agents may be naturally-occurring gums, for example, gum acacia or gum

tragacanth; naturally-occurring phosphatides, for example, soy bean, lecithin, and esters or partial esters derived from fatty acids; hexitol anhydrides, for example, sorbitan monooleate; and condensation products of partial esters with ethylene oxide, for example, polyoxyethylene sorbitan monooleate.

[00329] Formulations can also include carriers to protect the composition against rapid degradation or elimination from the body, such as a controlled release formulation, including implants, liposomes, hydrogels, prodrugs and microencapsulated delivery systems. For example, a time delay material such as glyceryl monostearate or glyceryl stearate alone, or in combination with a wax, may be employed.

[00330] The present disclosure contemplates the administration of a Modulator (e.g., a

Peptide) in the form of suppositories for rectal administration of the drug. The suppositories can be prepared by mixing the drug with a suitable non-irritating excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug. Such materials include, but are not limited to, cocoa butter and polyethylene glycols.

[00331] The Modulators contemplated by the present disclosure may be in the form of any other suitable pharmaceutical composition (e.g., sprays for nasal or inhalation use) currently known or developed in the future.

[00332] The concentration of a peptide or fragment thereof in a formulation can vary widely (e.g., from less than about 0.1%, usually at or at least about 2% to as much as 20% to 50%) or more by weight) and will usually be selected primarily based on fluid volumes, viscosities, and subject-based factors in accordance with, for example, the particular mode of administration selected.

Routes of Administration

[00333] The present disclosure contemplates the administration of the disclosed

Modulators, and compositions thereof, in any appropriate manner. Suitable routes of administration include parenteral (e.g., intramuscular, intravenous, subcutaneous (injection or implant), intraperitoneal, intracisternal, intraarticular, intraperitoneal, intracerebral

(intraparenchymal) and intracerebro ventricular), oral, nasal, vaginal, sublingual, intraocular, rectal, topical (e.g., transdermal), sublingual and inhalation.

[00334] Depot injections, which are generally administered subcutaneously or intramuscularly, may also be utilized to release the peptides disclosed herein over a defined period of time. Depot injections are usually either solid- or oil-based and generally comprise at least one of the formulation components set forth herein. One of ordinary skill in the art is familiar with possible formulations and uses of depot injections.

[00335] In an exemplary embodiment, an antibody or antibody fragment of the present disclosure is stored at 10 mg/ml in sterile isotonic aqueous saline solution for injection at 4°C and is diluted in either 100 ml or 200 ml 0.9% sodium chloride for injection prior to

administration to the subject. The antibody is administered by intravenous infusion over the course of 1 hour at a dose of between 0.2 and 10 mg/kg. In other embodiments, the antibody is administered by intravenous infusion over a period of between 15 minutes and 2 hours. In still other embodiments, the administration procedure is via subcutaneous bolus injection.

Combination Therapy

[00336] The present disclosure contemplates the use of the Modulators in combination with one or more active therapeutic agents or other prophylactic or therapeutic modalities. In such combination therapy, the various active agents frequently have different mechanisms of action. Such combination therapy may be especially advantageous by allowing a dose reduction of one or more of the agents, thereby reducing or eliminating the adverse effects associated with one or more of the agents; furthermore, such combination therapy may have a synergistic therapeutic or prophylactic effect on the underlying disease, disorder, or condition [00337] As used herein, "combination" is meant to include therapies that can be administered separately, e.g., formulated separately for separate administration (e.g., as may be provided in a kit), and therapies that can be administered together in a single formulation (i.e., a "co-formulation").

[00338] In certain embodiments, the Modulators are administered or applied sequentially, e.g., where one agent is administered before or one or more other agents. In other embodiments, the Modulators are administered simultaneously, e.g., where two or more agents are administered at or about the same time; the two or more agents may be present in two or more separate formulations or combined into a single formulation (i.e., a co-formulation). Regardless of whether the two or more agents are administered sequentially or simultaneously, they are considered to be administered in combination for purposes of the present disclosure.

[00339] The Modulators of the present disclosure can be used in combination with other agents useful in the treatment, prevention, suppression or amelioration of the diseases, disorders or conditions set forth herein, including those that are normally administered to subjects suffering from hyperglycemia, hyperinsulinemia, glucose intolerance, and other glucose metabolism disorders,.

[00340] The present disclosure contemplates combination therapy with numerous agents

(and classes thereof), including 1) insulin, insulin mimetics and agents that entail stimulation of insulin secretion, including sulfonylureas (e.g., chlorpropamide, tolazamide, acetohexamide, tolbutamide, glyburide, glimepiride, glipizide) and meglitinides (e.g., repaglinide (PRANDIN) and nateglinide (STARLIX)); 2) biguanides (e.g., metformin (GLUCOPHAGE)) and other agents that act by promoting glucose utilization, reducing hepatic glucose production and/or diminishing intestinal glucose output; 3) alpha-glucosidase inhibitors (e.g., acarbose and miglitol) and other agents that slow down carbohydrate digestion and consequently absorption from the gut and reduce postprandial hyperglycemia; 4) thiazolidinediones (e.g., rosiglitazone (AVANDIA), troglitazone (REZULIN), pioglitazone (ACTOS), glipizide, balaglitazone, rivoglitazone, netoglitazone, troglitazone, englitazone, ciglitazone, adaglitazone, darglitazone that enhance insulin action (e.g., by insulin sensitization), thus promoting glucose utilization in peripheral tissues; 5) glucagon-like -peptides including DPP-IV inhibitors (e.g., vildagliptin (GALVUS) and sitagliptin (JANUVIA)) and Glucagon-Like Peptide- 1 (GLP-1) and GLP-1 agonists and analogs (e.g., exenatide (BYETTA)); 6) and DPP-IV-resistant analogues (incretin mimetics), PPAR gamma agonists, dual-acting PPAR agonists, pan-acting PPAR agonists, PTP1B inhibitors, SGLT inhibitors, insulin secretagogues, RXR agonists, glycogen synthase kinase-3 inhibitors, immune modulators, beta-3 adrenergic receptor agonists, 1 lbeta-HSDl inhibitors, and amylin analogues.

[00341] Furthermore, the present disclosure contemplates combination therapy with agents and methods for promoting weight loss, such as agents that stimulate metabolism or decrease appetite, and modified diets and/or exercise regimens to promote weight loss.

[00342] The Modulators of the present disclosure may be used in combination with one or more other agent in any manner appropriate under the circumstances. In one embodiment, treatment with the at least one active agent and at least one Modulator of the present disclosure is maintained over a period of time. In another embodiment, treatment with the at least one active agent is reduced or discontinued (e.g., when the subject is stable), while treatment with the Modulator of the present disclosure is maintained at a constant dosing regimen. In a further embodiment, treatment with the at least one active agent is reduced or discontinued (e.g., when the subject is stable), while treatment with the Modulator of the present disclosure is reduced (e.g., lower dose, less frequent dosing or shorter treatment regimen). In yet another embodiment, treatment with the at least one active agent is reduced or discontinued (e.g., when the subject is stable), and treatment with the Modulator of the present disclosure is increased (e.g., higher dose, more frequent dosing or longer treatment regimen). In yet another embodiment, treatment with the at least one active agent is maintained and treatment with the Modulator of the present disclosure is reduced or discontinued (e.g., lower dose, less frequent dosing or shorter treatment regimen). In yet another embodiment, treatment with the at least one active agent and treatment with the Modulator of the present disclosure are reduced or discontinued (e.g., lower dose, less frequent dosing or shorter treatment regimen).

Dosing

[00343] The Modulators of the present disclosure may be administered to a subject in an amount that is dependent upon, for example, the goal of the administration (e.g., the degree of resolution desired); the age, weight, sex, and health and physical condition of the subject to be treated; the nature of the Modulator, and/or formulation being administered; the route of administration; and the nature of the disease, disorder, condition or symptom thereof (e.g., the severity of the dysregulation of glucose/insulin and the stage of the disorder). The dosing regimen may also take into consideration the existence, nature, and extent of any adverse effects associated with the agent(s) being administered. Effective dosage amounts and dosage regimens can readily be determined from, for example, safety and dose-escalation trials, in vivo studies (e.g., animal models), and other methods known to the skilled artisan.

[00344] In general, dosing parameters dictate that the dosage amount be less than an amount that could be irreversibly toxic to the subject (i.e., the maximum tolerated dose, "MTD") and not less than an amount required to produce a measurable effect on the subject. Such amounts are determined by, for example, the pharmacokinetic and pharmacodynamic parameters associated with absorption, distribution, metabolism, and excretion ("ADME"), taking into consideration the route of administration and other factors.

[00345] An effective dose (ED) is the dose or amount of an agent that produces a therapeutic response or desired effect in some fraction of the subjects taking it. The "median effective dose" or ED50 of an agent is the dose or amount of an agent that produces a therapeutic response or desired effect in 50% of the population that takes it. Although the ED ₅ o is commonly used as a measure of reasonable expectance of an agent's effect, it is not necessarily the dose that a clinician might deem appropriate taking into consideration all relevant factors. Thus, in some situations the effective amount is more than the calculated ED 50, in other situations the effective amount is less than the calculated ED ₅₀ , and in still other situations the effective amount is the same as the calculated ED ₅ o.

[00346] In addition, an effective dose of the Modulators of the present disclosure may be an amount that, when administered in one or more doses to a subject, produces a desired result relative to a healthy subject. For example, an effective dose may be one that, when administered to a subject having elevated plasma glucose and/or plasma insulin, achieves a desired reduction relative to that of a healthy subject by at least about 10%>, at least about 20%>, at least about 25%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, or more than 80%.

[00347] An appropriate dosage level will generally be about 0.001 to 100 mg per kg patient body weight per day which can be administered in single or multiple doses. In some embodiments, the dosage level will be about 0.01 to about 25 mg/kg per day, and in other embodiments about 0.05 to about 10 mg/kg per day. A suitable dosage level may be about 0.01 to 25 mg/kg per day, about 0.05 to 10 mg/kg per day, or about 0.1 to 5 mg/kg per day. Within this range, the dosage may be 0.005 to 0.05, 0.05 to 0.5 or 0.5 to 5.0 mg/kg per day.

[00348] For administration of an oral agent, the compositions can be provided in the form of tablets, capsules and the like containing from 1.0 to 1000 milligrams of the active ingredient, particularly 1.0, 3.0, 5.0, 10.0, 15.0, 20.0, 25.0, 50.0, 75.0, 100.0, 150.0, 200.0, 250.0, 300.0, 400.0, 500.0, 600.0, 750.0, 800.0, 900.0, and 1000.0 milligrams of the active ingredient for the symptomatic adjustment of the dosage to the patient to be treated. The compounds may be administered on a regimen of 1 to 4 times per day, and often once or twice per day.

[00349] The dosage of the Modulators of the present disclosure may be repeated at an appropriate frequency which may be in the range once per day to once every three months, depending on the pharmacokinetics of the Modulators (e.g. half-life of the antibody in the circulation) and the pharmacodynamic response (e.g. the duration of the therapeutic effect of the Modulator). In some embodiments where the Modulator is an antibody or a fragment thereof, or a peptide or variants thereof, dosing is repeated between once per week and once every 3 months. In other embodiments, the antibody is administered approximately once per month.

[00350] In certain embodiments, the dosage of the disclosed Modulators is contained in a

"unit dosage form". The phrase "unit dosage form" refers to physically discrete units, each unit containing a predetermined amount of a Modulator of the present disclosure, either alone or in combination with one or more additional agents, sufficient to produce the desired effect. It will be appreciated that the parameters of a unit dosage form will depend on the particular agent and the effect to be achieved.

KITS

[00351] The present disclosure also contemplates kits comprising the disclosed

Modulators, and pharmaceutical compositions thereof. The kits are generally in the form of a physical structure housing various components, as described below, and may be utilized, for example, in practicing the methods described above (e.g., administration of a Modulator to a subject in need of restoring glucose homeostasis).

[00352] A kit can include one or more of the Modulators disclosed herein (provided in, e.g., a sterile container), which may in the form of a pharmaceutical composition suitable for administration to a subject. The Modulators can be provided in a form that is ready for use or in a form requiring, for example, reconstitution or dilution prior to administration. When the Modulators are in a form that needs to be reconstituted by a user, the kit may also include buffers, pharmaceutically acceptable excipients, and the like, packaged with or separately from the Modulators. When combination therapy is contemplated, the kit may contain the several agents separately or they may already be combined in the kit. Each component of the kit can be enclosed within an individual container and all of the various containers can be within a single package. A kit of the present disclosure can be designed for conditions necessary to properly maintain the components housed therein (e.g., refrigeration or freezing).

[00353] A kit may contain a label or packaging insert including identifying information for the components therein and instructions for their use (e.g., dosing parameters, clinical pharmacology of the active ingredient(s), including mechanism of action, pharmacokinetics and pharmacodynamics, adverse effects, contraindications, etc.). Labels or inserts can include manufacturer information such as lot numbers and expiration dates. The label or packaging insert may be, e.g., integrated into the physical structure housing the components, contained separately within the physical structure, or affixed to a component of the kit (e.g., an ampoule, tube or vial). Exemplary instructions include those for reducing or lowering blood glucose, treatment of hyperglycemia, treatment of diabetes, etc. with the disclosed Modulators, and pharmaceutical compositions thereof.

[00354] Labels or inserts can additionally include, or be incorporated into, a computer readable medium, such as a disk (e.g., hard disk, card, memory disk), optical disk such as CD- or DVD-ROM/RAM, DVD, MP3, magnetic tape, or an electrical storage media such as RAM and ROM or hybrids of these such as magnetic/optical storage media, FLASH media or memory type cards. In some embodiments, the actual instructions are not present in the kit, but means for obtaining the instructions from a remote source, e.g., via the internet, are provided.

EXPERIMENTAL

[00355] The following examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how to make and use the present invention, and are not intended to limit the scope of what the inventors regard as their invention nor are they intended to represent that the experiments below are all or the only experiments performed. Efforts have been made to ensure accuracy with respect to numbers used (e.g., amounts, temperature, etc.), but some experimental errors and deviations should be accounted for.

[00356] Unless indicated otherwise, parts are parts by weight, molecular weight is weight average molecular weight, temperature is in degrees Celsius (°C), and pressure is at or near atmospheric. Standard abbreviations are used, including the following: bp = base pair(s); kb = kilobase(s); pi = picoliter(s); s or sec = second(s); min = minute(s); h or hr = hour(s); aa = amino acid(s); kb = kilobase(s); nt = nucleotide(s); ng = nanogram; μg = microgram; mg = milligram; g = gram; kg = kilogram; dl or dL = deciliter; μΐ or μΐ, = microliter; ml or mL = milliliter; 1 or L = liter; μΜ = micromolar; mM = millimolar; M = molar; i.m. = intramuscular(ly); i.p. =

intraperitoneal(ly); s.c. = subcutaneous(ly); HPLC = high performance liquid chromatography; MALDI-TOF = matrix-assisted laser desorption/ionization time-of-fiight (MALDI-TOF); BW = body weight; U = unit; FPG = fasting plasma glucose; FPI = fasting plasma insulin; ITT = insulin tolerance test; PTT = pyruvate tolerance test; oGTT = oral glucose tolerance test; GSIS = glucose-stimulated insulin secretion; PBS = phosphate -buffered saline; ECCs = enteroendocrine cells; ECs = enterocytes; and FPKM = fragments per kilobase of exon per million fragments mapped.

Materials and Methods

[00357] The following methods and materials were used in the Examples below:

[00358] Peptide Analysis. The full-length Ednl, Habp2, Kazaldl, Respl8 and Tinag precursors were subjected to analysis to identify putative processing sites using previously described bioinformatic methods. (See Samson et al, J. Biol. Chem. 283:31949 (2008)). Briefly, Ednl, Habp2, Kazaldl, Respl8 and Tinag sequences from mammalian species were aligned, and putative processing sites identified based on conservation of flanking mono- or di-basic processing sites.

[00359] Peptide Synthesis. Solid-phase peptide synthesis was performed by Abgent (San Diego, CA) or iBioSource (Foster City, CA). Peptide purity was assessed using reverse phase HPLC and/or MALDI-TOF mass spectrometry.

[00360] Animals. Eight-week old male C57BL/6 mice were purchased from the Charles

River Laboratory (Wilmington, MA). Mice were kept in accordance with welfare guidelines under controlled light (12 hr light and 12 hr dark cycle, dark 6:30 p.m. - 6:30 a.m.), temperature (22±4°C) and humidity (50%±20%) conditions. Mice had free access to water (autoclaved distilled water) and were fed ad libitum on a high-fat diet (D 12492, Research Diets, New Brunswick, NJ) containing 60 kcal% fat, 20 kcal% protein and 20 kcal% carbohydrate for a minimum of 12 weeks to induce obesity and systemic insulin resistance. All animal studies were approved by the NGM Institutional Animal Care and Use Committee for NGM-7-2008 entitled "Effect of gastrointestinal bypass surgery on systemic insulin sensitivity in rodent models of obesity, insulin resistance and type 2 diabetes".

[00361] Body Weight. Body weight was determined prior to all metabolic tests using an automated digital scale (Sartorius LE5201, Sartorius Mechatronics Corp., Bohemia, NY) equipped with Software Wedge (Sartorius YSW05, Sartorius Mechatronics Corp., Bohemia, NY).

[00362] Metabolic Studies. The high-fat fed mice were randomly assigned to vehicle control or peptide groups for each of the metabolic studies described hereafter. All groups (n = 6 mice per group) were matched for age and body weight, and the average body weight for each group of mice in each study was -50 g.

[00363] Fasting Plasma Glucose and Fasting Plasma Insulin. Basal glucose and insulin concentrations (i.e., FPG and FPI, respectively) were determined in untreated mice following a 4-hour fast (e.g., at min-30 in Figure 5, Panels a and c, respectively). In addition, the effect of peptide or vehicle administration on FPG and FPI was determined at minO prior to oGTT or GSIS (i.e., 30 minutes-post peptide or vehicle treatment; see, e.g., Figure 5, Panels a and c, respectively). Blood samples were taken from mice via tail vein. FPG concentration was determined using the Mutarotase-GOD enzymatic assay (Wako Diagnostics Inc, Richmond, VA). FPI concentration was determined by a mouse ultra-sensitive enzyme-linked

immunosorbent assay (ALPCO Diagnostics, Salem, NH).

[00364] Oral Glucose Tolerance Test (oGTT). Following a 4 hr fast, mice received a single bolus i.p. injection of peptide or vehicle control at min-30. At minO, glucose (lg/kg) in PBS was administered orally. Plasma glucose concentration was determined at -30, 0, 15, 60 and 120 minutes by the Mutarotase-GOD enzymatic assay (Wako Diagnostics Inc, Richmond, VA). All measurements were made by taking blood samples from the tail vein. oGTT was used to assess glucose tolerance. [00365] Glucose-stimulated Insulin Secretion (GSIS). Following a 4 hr fast, mice received a single bolus i.p. injection of peptide or vehicle control at min-30. At minO, mice received glucose (lg/kg) in PBS orally. Plasma insulin concentration was determined at -30, 0, 15 and 60 minutes by a mouse ultra-sensitive enzyme-linked immunosorbent assay (ALPCO Diagnostics, Salem, NH). All measurements were made by taking blood samples from the tail vein. GSIS was used to assess insulin secretion in response to a glucose challenge.

[00366] Statistics. Statistical analysis was performed with Student's t-Test with 2-tailed distribution.

Example 1: Ednl Gene Expression

[00367] EECs and ECs were isolated from the mouse duodenum, jejunum, ileum and colon. Ednl gene expression was then measured in FACS-sorted cells using SOLiD deep sequencing technology as directed by the manufacturer (Applied Biosystems, Foster City, CA, USA).

[00368] Ednl gene expression data (measured in units of FPKM) are set forth in Figure 1.

As indicated in Figure 1, Ednl gene expression is prevalent in EECs of the colon and is either below the level of detection or is not expressed in the jejunum, duodenum and ileum. Ednl gene expression in ECs is either below the level of detection or is not expressed in the duodenum, jejunum, ileum or colon.

Example 2: Effect of Ednl Murine Peptide-pl on Glucose Homeostasis in High-fat Fed Obese, Insulin-resistant Mice

[00369] The glucoregulatory effects of murine Ednl Murine Peptide-pl on glucose homeostasis were evaluated. Twenty-two week-old high-fat fed mice weighing approximately 50 g were injected i.p. with a single dose of Ednl Murine Peptide-pl or vehicle control, and plasma glucose and insulin concentrations were determined. Basal (fasted) plasma glucose (FPG) concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Ednl Murine Peptide-pl (lOmg/kg) or vehicle control, and at minO glucose (1 g/kg) in PBS was administered orally. Plasma glucose concentrations were determined at -30, 0, 15, 60 and 120 minutes. [00370] Figure 5, Panel a shows the effect of a single bolus i.p. injection of Ednl Murine

Peptide- l (gray squares) and vehicle control (black squares) on basal (fasted) plasma glucose concentration and on oral glucose tolerance, whereas Figure 5, Panel b shows the data from Figure 5, Panel a expressed as the percent change in plasma glucose concentration normalized to baseline (min-30). As indicated in Figure 5, Panel a, Ednl Murine Peptide-pl increased plasma glucose concentration at 15 and 60 minutes in a statistically significant manner, but did not significantly increase FPG concentration. When the data are normalized to baseline, there is a trend towards worsening oral glucose tolerance at each time point (see Figure 5, Panel b).

[00371] Basal (fasted) plasma insulin (FPI) and glucose-stimulated insulin secretion

(GSIS) concentrations were evaluated in a manner similar to that utilized for plasma glucose. Briefly, FPI concentrations were determined in untreated high-fat fed mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Ednl Murine Peptide-pl or vehicle control, and at minO glucose (1 g/kg) in PBS was administered orally. Plasma insulin concentrations were determined at -30, 0, 15 and 60 minutes. Figure 5, Panel c shows the effect of a single bolus i.p. injection of Ednl Murine Peptide-pl (gray squares) and vehicle control (black squares) on FPI and GSIS concentrations, whereas Figure 5, Panel d shows the data from Figure 5, Panel c expressed as the percent change in plasma insulin concentration normalized to baseline (min-30). As indicated in Figure 5, Panel c, Ednl Murine Peptide-pl decreased FPI concentration and GSIS concentration at 15 minutes in a statistically significant manner. When the data are normalized to baseline, there is a trend towards decreasing both FPI concentration and GSIS concentration (see Figure 5, Panel d). (n = 6 mice per group; p-values determined by a student's t-test comparing Ednl Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[00372] These data indicate that an inhibitor of Endl peptide function may result in a positive effect on glucose homeostasis.

Example 3: Habp2 Gene Expression

[00373] EECs and ECs were isolated from the mouse duodenum, jejunum, ileum and colon. Habp2 gene expression was then measured in FACS-sorted cells using SOLiD deep sequencing technology as directed by the manufacturer (Applied Biosystems, Foster City, CA, USA). [00374] Habp2 gene expression data (measured in units of FPKM) are set forth in Figure

6. As indicated in Figure 6, Habp2 gene expression is prevalent in EECs of the duodenum and is either below the level of detection or is not expressed in the jejunum, ileum and colon. Habp2 gene expression in ECs is either below the level of detection or is not expressed in the duodenum, jejunum, ileum or colon.

Example 4: Effect of Habp2 Murine Peptide-pl on Glucose Homeostasis in High-fat Fed Obese, Insulin-resistant Mice

[00375] The glucoregulatory effects of murine Habp2 Murine Peptide-pl on glucose homeostasis were evaluated as described in Example 2. Briefly, twenty-two week-old high-fat fed mice weighing approximately 50 g were injected i.p. with a single dose of Habp2 Murine Peptide-pl or vehicle control, and plasma glucose and insulin concentrations were determined. Basal (fasted) plasma glucose (FPG) concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Habp2 Murine Peptide-pl (lOmg/kg) or vehicle control, and at minO glucose (1 g/kg) in PBS was administered orally. Plasma glucose concentrations were determined at -30, 0, 15, 60 and 120 minutes.

[00376] Figure 10, Panel a shows the effect of a single bolus i.p. injection of Habp2

Murine Peptide-pl (gray squares) and vehicle control (black squares) on basal (fasted) plasma glucose concentration and on oral glucose tolerance, whereas Figure 10, Panel b shows the data from Figure 10a expressed as the percent change in plasma glucose concentration normalized to baseline (min-30). As indicated in Figure 10, Panel a and b, administration of Habp2 Murine Peptide-pl resulted in increased FPG concentration and oral glucose tolerance concentration at 60 minutes in a statistically significant manner.

[00377] Basal (fasted) plasma insulin (FPI) and GSIS concentrations were evaluated in a manner similar to that utilized for plasma glucose. Briefly, FPI concentrations were determined in untreated high-fat fed mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Habp2 Murine Peptide-pl or vehicle control, and at minO glucose (1 g/kg) in PBS was administered orally. Plasma insulin concentrations were determined at -30, 0, 15 and 60 minutes. Figure 10, Panel c shows the effect of a single bolus i.p. injection of Habp2 Murine Peptide-pl (gray squares), and vehicle control (black squares) on FPI concentration and on glucose-stimulated insulin secretion (GSIS), whereas Figure 10, Panel d shows the data from Figure 10, Panel c expressed as the percent change in plasma insulin concentration normalized to baseline (min-30). As indicated in Figure 10, Panel c, Habp2 Murine Peptide-pl decreased GSIS concentration at the 15 minute time point in a statistically significant manner, and there was a trend toward decreasing FPI concentration and GSIS concentration at the other time points. When these data are normalized to baseline, Habp2 Murine Peptide-pl worsened both FPI and GSIS in a statistically significant manner (see Figure 10, Panel d). (n = 6 mice per group; p- values determined by a student's t-test comparing Habp2 Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[00378] These data indicate that an inhibitor of Habp2 peptide function may result in a positive effect on glucose homeostasis.

Example 5: Kazaldl Gene Expression

[00379] EECs and ECs were isolated from the mouse duodenum, jejunum, ileum and colon. Kazaldl gene expression was then measured in FACS-sorted cells using SOLiD deep sequencing technology as directed by the manufacturer (Applied Biosystems, Foster City, CA, USA).

[00380] Kazaldl gene expression data (measured in units of FPKM) are set forth in Figure

11. As indicated in Figure 11 , Kazaldl gene expression is prevalent in EECs of the duodenum and is either below the level of detection or is not expressed in the jejunum, ileum and colon. Kazaldl gene expression in ECs is either below the level of detection or is not expressed in the duodenum, jejunum, ileum and colon.

Example 6: Effect of Kazaldl Murine Peptide-pl on Glucose Homeostasis in High-fat Fed Obese, Insulin-resistant Mice

[00381] The glucoregulatory effects of Kazaldl Murine Peptide-pl on glucose homeostasis were evaluated as described in Example 2. Briefly, twenty-two week-old high-fat fed mice weighing approximately 50 g were injected i.p. with a single dose of Kazaldl Murine Peptide-pl or vehicle control, and plasma glucose and insulin concentrations were determined. Basal (fasted) plasma glucose (FPG) concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Kazaldl Murine Peptide -pi (lOmg/kg) or vehicle control, and at minO glucose (1 g/kg) in PBS was administered orally. Plasma glucose concentrations were determined at -30, 0, 15, 60 and 120 minutes.

[00382] Figure 14, Panel a shows the effect of a single bolus i.p. injection of Kazaldl

Murine Peptide -pi (gray squares) and vehicle control (black squares) on basal (fasted) plasma glucose concentration and on oral glucose tolerance, whereas Figure 14, Panel b shows the data from Figure 14, Panel a expressed as the percent change in plasma glucose concentration normalized to baseline (min-30). As indicated in Figure 14, Panel a, Kazaldl Murine Peptide-pl increased plasma glucose concentration at the 60 minute time point in a statistically significantly manner, and, when the data were normalized to baseline, increased plasma glucose concentration at 120 minutes (see Figure 14, Panel b). A trend is observed of Kazaldl Murine Peptide-pl worsening FPG concentration and glucose tolerance at all time points.

[00383] Basal (fasted) plasma insulin (FPI) and GSIS concentrations were evaluated in a manner similar to that utilized for plasma glucose. Briefly, FPI concentrations were determined in untreated high-fat fed mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Kazaldl Murine Peptide-pl or vehicle control, and at minO glucose (1 g/kg) in PBS was administered orally. Plasma insulin concentrations were determined at -30, 0, 15 and 60 minutes. Figure 14, Panel c shows the effect of a single bolus i.p. injection of Kazaldl Murine Peptide-pl (gray squares), and vehicle control (black squares) on FPI concentration and on glucose-stimulated insulin secretion (GSIS), whereas Figure 14, Panel d shows the data from Figure 14, Panel c expressed as the percent change in plasma insulin concentration normalized to baseline (min-30). As indicated in Figure 14, Panel c, Kazaldl Murine Peptide-pl worsened plasma insulin concentrations, and this trend was statistically significant at the 15 minute time point when the data were normalized to baseline (see Figure 14, Panel d). (n = 6 mice per group; p-values determined by a student's t-test comparing Kazaldl Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[00384] These data indicate that an inhibitor of Kazaldl peptide function may result in a positive effect on glucose homeostasis. Example 7: Respl8 Gene Expression

[00385] EECs and ECs were isolated from the mouse duodenum, jejunum, ileum and colon. Kazaldl gene expression was then measured in FACS-sorted cells using SOLiD deep sequencing technology as directed by the manufacturer (Applied Biosystems, Foster City, CA, USA).

[00386] Respl8 gene expression data (measured in units of FPKM) are set forth in Figure

15. As indicated in Figure 15, Respl8 gene expression is most prevalent in EECs of the colon and is observed to a lesser extent in EECs of the duodenum, jejunum and ileum. Respl81 gene expression in ECs is either below the level of detection or is not expressed in the duodenum, jejunum, ileum and colon.

Example 8: Effect of Respl8 Murine Peptide-pl on Glucose Homeostasis in High-fat Fed Obese, Insulin-resistant Mice

[00387] The glucoregulatory effects of Respl8 Murine Peptide-pl on glucose homeostasis were evaluated as described in Example 2. Briefly, twenty-two week-old high-fat fed mice weighing approximately 50 g were injected i.p. with a single dose of Respl8 Murine Peptide-pl or vehicle control, and plasma glucose and insulin concentrations were determined. Basal (fasted) plasma glucose (FPG) concentrations were determined in untreated mice following a 4- hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Respl8 Murine Peptide-pl (lOmg/kg) or vehicle control, and at minO glucose (1 g/kg) in PBS was administered orally. Plasma glucose concentrations were determined at -30, 0, 15, 60 and 120 minutes.

[00388] Figure 19, Panel a shows the effect of a single bolus i.p. injection of Respl8 Murine Peptide-pl (gray squares) and vehicle control (black squares) on basal (fasted) plasma glucose concentration and on oral glucose tolerance, whereas Figure 19, Panel b shows the data from Figure la expressed as the percent change in plasma glucose concentration normalized to baseline (min-30). As indicated in Figure 19, Panels a and b, upon administration of Respl8 Murine Peptide-pl there is a trend toward increasing plasma glucose concentration at each time point.

[00389] Basal (fasted) plasma insulin (FPI) and GSIS concentrations were evaluated in a manner similar to that utilized for plasma glucose. Briefly, FPI concentrations were determined in untreated high-fat fed mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Res l8 Murine Peptide -pi or vehicle control, and at minO glucose (1 g/kg) in PBS was administered orally. Plasma insulin concentrations were determined at -30, 0, 15 and 60 minutes. Figure 19c shows the effect of a single bolus i.p. injection of Respl8 Murine Peptide -pi (gray squares), and vehicle control (black squares) on FPI concentration and on glucose-stimulated insulin secretion (GSIS), whereas Figure 19, Panel d shows the data from Figure 19, Panel c expressed as the percent change in plasma insulin concentration normalized to baseline (min-30). As indicated in Figuresl9, Panels c and d, upon administration of Respl8 Murine Peptide -pi there is a trend toward decreasing plasma insulin concentration at each time point, (n = 6 mice per group; p-values determined by a student's t-test comparing Respl8 Murine Peptide-pl and Vehicle-treated mice are indicated above the bars.)

[00390] These data indicate that an inhibitor of Resp 18 peptide function may result in a positive effect on glucose homeostasis.

Example 9: Tinag Gene Expression

[00391] EECs and ECs were isolated from the mouse duodenum, jejunum, ileum and colon. Kazaldl gene expression was then measured in FACS-sorted cells using SOLiD deep sequencing technology as directed by the manufacturer (Applied Biosystems, Foster City, CA, USA).

[00392] Tinag gene expression data (measured in units of FPKM) are set forth in Figure

20. As indicated in Figure 20, Tinag gene expression is prevalent in EECs of the duodenum and ileum and is either below the level of detection or is not expressed in the jejunum and colon. Tinag gene expression in ECs is observed in the duodenum and is either below the level of detection or is not expressed in the jejunum, ileum and colon.

Example 10: Effect of Tinag Murine Peptides-p3 and -p4 on Glucose Homeostasis in High- fat Fed Obese, Insulin-resistant Mice

[00393] The glucoregulatory effects of Tinag Murine Peptides-p3 and -p4 on glucose homeostasis were evaluated as described in Example 2. Briefly, twenty-two week-old high- fat fed mice weighing approximately 50 g were injected i.p. with a single dose of either Tinag Murine Peptide -p3, Tinag Murine Peptide -p4 or vehicle control, and plasma glucose and insulin concentrations were determined. Basal (fasted) plasma glucose (FPG) concentrations were determined in untreated mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Tinag Murine Peptides-p3 (lOmg/kg), Tinag Murine Peptides-p4 (lOmg/kg), or vehicle control, and at minO glucose (1 g/kg) in PBS was administered orally. Plasma glucose concentrations were determined at -30, 0, 15, 60 and 120 minutes.

[00394] Figure 24 Panel a shows the effect of a single bolus i.p. injection of Tinag Murine

Peptide-p3 (gray squares) and vehicle control (black squares) on basal (fasted) plasma glucose concentration and on oral glucose tolerance, whereas Figure 24, Panel b shows the data from Figure 24, Panel a expressed as the percent change in plasma glucose concentration normalized to baseline (min-30). As indicated in Figure 24, Panel a, Tinag Murine Peptide -p3 increased plasma glucose concentration in a statistically significant manner at the 50 minute time point, and, when the data from Figure 24, Panel a are normalized to baseline, administration of Tinag Murine Peptide -p3 increased plasma glucose concentrations in a statistically significant manner at the 60- and 120-minute time points (see Figure 24, Panel b)

[00395] Basal (fasted) plasma insulin (FPI) and GSIS concentrations were evaluated in a manner similar to that utilized for plasma glucose. Briefly, FPI concentrations were determined in untreated high-fat fed mice following a 4-hour fast (min-30). Thereafter, mice received a single bolus i.p. injection of Tinag Murine Peptide -p3 or vehicle control, and at minO glucose (1 g/kg) in PBS was administered orally. Plasma insulin concentrations were determined at -30, 0, 15 and 60 minutes. Figure 24, Panel c shows the effect of a single bolus i.p. injection of Tinag Murine Peptide -p3 (gray squares) and vehicle control (black squares) on FPI concentration and on glucose-stimulated insulin secretion (GSIS), whereas Figure 24, Panel d shows the data from Figure 24c expressed as the percent change in plasma insulin concentration normalized to baseline (min-30). As indicated in Figure 24, Panels c and d, upon administration of Tinag Murine Peptide -p3 there is a trend toward decreasing plasma insulin concentration at each time point, (n = 6 mice per group; p-values determined by a student's t-test comparing Tinag Murine Peptide-p3 and Vehicle-treated mice are indicated above the bars.)

[00396] Data were generated for Tinag Murine Peptide -p4 in a manner analogous to that described for Tinag Murine Peptide -p3. As indicated in Figure 25, Panel a and b, Tinag Murine Peptide-p4 (gray squares) increased plasma glucose concentrations compared to vehicle control (black squares) in a statistically significant manner at the 60 minute time point, and there was a trend toward increased plasma glucose concentrations at the other time points. [00397] Figure 25, Panels c and d indicate that Tinag Murine Peptide-p4 (gray squares) decreased FPI or GSIS concentrations compared to vehicle control (black squares), but that this decrease was not statistically significant, (n = 6 mice per group; p-values determined by a student's t-test comparing Tinag Murine Peptide -p4 and Vehicle-treated mice are indicated above the bars.)

[00398] In view of the data described above, an inhibitor of Tinag Murine Peptides-p3 and/or -p4 function may result in a positive effect on glucose homeostasis.

[00399] Particular embodiments of this invention are described herein, including the best mode known to the inventors for carrying out the invention. Upon reading the foregoing, description, variations of the disclosed embodiments may become apparent to individuals working in the art, and it is expected that those skilled artisans may employ such variations as appropriate. Accordingly, it is intended that the invention be practiced otherwise than as specifically described herein, and that the invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law.

Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly

contradicted by context.

[00400] All publications, patent applications, accession numbers, and other references cited in this specification are herein incorporated by reference as if each individual publication or patent application were specifically and individually indicated to be incorporated by reference.