CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority Ip U.S. Provisional Application Serial No, 62/866,741* filed June 26, 2019, and U.S. Provisional Application Serial No. 63/012,568, filed April 20, 2020, each of which is incorporated herein by reference in its entirety

FIELD OF THE IN VENTION

19001 [ The resent invention is in the fields of molecular biology, virology, and gene therapy. More particularly, the invention relates to a baculovi ys system for th synthesis of recombinant protein in insect cells

BACKGROUND OF THE INVENTION

[9002] Gene therapy hits been developed to treat a number of disorders such as carreer and genetic related diseases. Such treatment includes the use of recombinant proteins w hich have been produced in mammalian systems using viral vectors

[9093] Currently there arc several technologies in the field of recombinant protein and viral vector production which use different means of introducing foreign ge es into the host ceils. For example, traditional met ods of introducing AAV genes utilize f!ietransfection of mammalian cell hues suc as HEK-293 or Bela cells with triple or double plasmids (Xiao, Li t al 1998, Grimm, Kay ei al 2003). Another technique htil es Herpes simplex virus (HSV) to infect mammalia cells, e.g., for AAV mamifactur g (Zhang, De Alwis-etuL 19 9)

|9094| Unfortunately, AAV production in these systems has been low. For example*

A AV vector production has been hampered by the difficulties of generating sufficient HSV seed stocks. Also the anufacture of AAV vectors: is difficult to scale up due to the inherent properties of adherent mammalian cells and low yield of AAV production, Tims, large scale production of AAV in these systems sufficient to obtain enough material ibr clinical trials has been problematic.

}0ίKί5| Other recombinant protein and viral productio s stems include the use of baculovinis in insect cells (Chen 2008, Kotin 201 1 ). The baculovinis expression vector (of bacmid) System (REVS) is a well-established metho for the production of recombinant proteins to he used as vaccines, therapeutic molecules, or diagnostic reagents (van Gets, Pijlman ef a/. 2013). This ystem provides increased AAV production yields relative to other AAV production technologies (Galibert and Merten 201 i ). However, this method has encountered AAV capsid degradation:. Removal of the baculovims chitinase (chiAj and cathepsin (v-caik) genes has bees reported to improve the integrity of secreted recombinant proteins and prevente AAV8 capsid degradation (Galibert. Savy el aί 2018), However, removal of the chid gene alsoremo es the chitinase activity that is required to breakdown the chitin, a high molecular weight linear polymer: of iNi-aeeiyhD-glueosainine units synthesized in the insect cells (fshimwe, Hodgson ccof 2015), Without vh 4 activity _* the: AAV particles produced in these insect cells are difficult to isolate from, the viscous edi lysate, thereby reducing the recovery of AAV particles,.

(00061 Therefore, improved expression systems that produce useful amounts of recombinant viral vectors an proteins that are not degraded and that have useful levels of activity are needed,

SUMMARY OF THE INVENTION

1 071 It has been discovered that a recombinant baculovims (rBV) having a genome with a deietion of the v-mrh gene enables the expression of AAV capsid proteins with higher structural integrity, from a cassette that has been integrated into the rBV genome. Therefore, «AAV isolatedfront insect-qells infected with rwi&i wfw-deleted rBV have higher iofeetivity than rA AV isolated from insect cells infected with rBV containing cathepsin,

|0008| These disco veries have been exploited to develop the present disclosure, which, in part, is directed to a .recombinant baculovims system, the components thereof, and to methods using a specifically deleted rBV for foreign protein expression. 10009] In one aspect, the disclosure provides a recombinant baeuiowus (rBV) DNA backbone, comprising: a: chitinase gene; a deletion of the v-cath gene; and a DNA fragment enabl ing integration of one or more foreign protein expression cassettes into the backbone, such that the one or more foreign protein or proteins expressed in an insect cell are less degraded than they are when expressed from a rBV backbone without the deletion.

[0010] In some embodiments, the DNA fragment comprises a DN A sequence homologous to two sequences flanking the one or more foreign protein expression cassetes in a donor plasmid. In certain embodiments, the DNA fragment is derived from bM ON 14272. In some embodiments, the DNA fragment comprises ad origin of replication. In specific embodiments, the origin of replication is a mini-F-rep!ieon _s ColEL oriC, OriV On For OriS,

In certain embodiments, the DNA fragment further comprises a reporter gene, in specific embodiments, the reporter gene is LacZa.

10011] In some embodiments, the rB V D A backbone further comprises a selection marker expression gene cassete integrated into the eath-y deletion in particular embodiments, the selection marker expression gene cassete comprises an antibiotic-resistance gene, and in particular embodiments, the anti biotic-resistance gene is a kanarnycin-resistaut gene, an amptciliin -resistant gene, afefmcyciine-resistant gene, a geniam ici rcSistant gene, a blastieidin-resistasce gette, a chloramphenicol-resistance gene, a streptomycin -resistance gene, or a genctid -resistance gene. In other embodiments, the selection marker expression gene cassette comprises a selection marker gene encoding a visually detectable protein, In some embodiments, the selection marker gene encodes a colorimetric, fluorescent, chromatographic, chemiluminescent, or luminescent protein,

[0012] The present discourse also provides a recombinant baculo virus (rBV) genome comprising: a rBV DNA backbone; and a foreign protein expression cassette. The rB V DNA backbone comprises: a chitinase genera deletion of the v-cath gene; and a DNA fragment enabling integration of one or more foreign protein expression cassettes into the backbone, such that the one or more foreign protein or proteins expressed in an insect cel l are less degraded than they arc when expressed from a rBV backbone without the deletion. The foreign protein gene cassette comprises: at least one foreign protein gene; an insect cell promoter operably linked to the at least one foreign gene; and two DMA sequences, enabling the foreig protein expression cassette to integrate into the rBV DNA backbone.

J0013J In some embodiments _» the at least one foreign protein gene in the foreign expression cassette compromises at least one viral protein gene and or at least one mammalian protein gene in certain embodiments, the viral protein .gene encodes an AV protein, an adenoviral protein, a retroviral protein, an SV40 protein, or a Herpes si plex viral proteim Tn specific embodiments, the foreign protein expression cassette comprises a sequence encoding at least one AAV capsid protein. In certain embodiments, the at least one AAV protein is VP L VP2, VP3, and/or a Re protein, and in particular embodiments, the at least one $V40 protein is V P I major capsid protein.

1 0141 In some embodiments, the foreign protein expression cassette comprises an insect promoter _» such as a polyhedron, p lO, or 6,9 insect promoter, operably linked to the at least one foreign protein gene. 0015] In some embodiments, the tw DNA sequences enabling the foreign protei expression cassette to integrate into th DN A backbone are homologous to the DNA sequence in the rBV DMA backbone. In particular embodiments, the two DMA sequences enabling the foreign protein expression cassette to integrate into the DNA backbone are iransposable elements in certain embodiments, the two DNA sequences enabling the foreign protein expression cassette, to integrate into the DNA backbone are Tn7R and Tir7L

100101 In another aspect, th disclosure provides a recombinant baeuloviras (rB V) genome, comprising: a rBV DNA backbone and a foreign protein cassete. The rBV backbone comprises: a chitinase gene; a deletion of the v-caih gene; a selection raarkergene cassette integrated into the cath v deletion; and a DMA fragment enabling integration of one or more foreign protein expression -cassettes into the back one, such that the one or more foreign protein Of proteins expressed in an insect cell are less degraded than they are when expressed from a rBV backbone withou the deletion. The foreign protein expression cassette comprises: at; least one foreign protein gene; an insect cell promoter operably linked to the at least one foreign gene; and two DNA sequences, enabling the foreign protein expression cassette to integrate into the rBV D A backbone.

[0017] In yet another aspect, the disclosure provides a recombinant bacuiovirus (rBV) vector or particle comprising: an rBV genome; an at least one baculoviral capsid protein. The rBV genome comprises: an rB V DN A backbone; and a foreign protein e pression cassette, the rBV DMA backbone comprising: a chitinase gene; a deletion of the v-caik gene and a DMA fragment enabling integration of one or more foreign protein expression cassettes into the backbone, such that the one or more foreign protein or proteins expressed in an insect cell are less degraded than they are when expressed from a rBV backbone without the deletion, and the foreign protein gene cassette comprises; at least one foreign protein gene; an insect cell promoter operab!y linked to the at least one foreign gene; and two DMA sequences, enabling the foreign protein expression cassette to integrate into lire rBV DNA backbone, in some embodiments, the rB V genome comprises a rB V backbone comprising a foreign protein expression cassette encoding at least one AAV capsid protein.

|00I8] In stil l another aspect, the disclosure provides a recombinant bacuiovirus (rBV) vector or particle comprising: aiBV genome; and at least one haculoviral capsid protein. The rBV genome comprises: an rBV DNA backbone comprising: a chitinase gene; a deletion of the v~cath gene; a selection marker gene cassette integrated into the ath~v deletion; and a DNA fragment enabling integration of one or more foreign protein expression cassettes into the backbone, such that the one or more foreign protein or proteins expressed in an insect cell are less degrade than they are when expressed from a rBV backbone without the deletion, The foreign protein expression cassette comprises: at least one foreign protein gene; an insect cell promoter uperahly linked to the at least one foreign gene; and two D A sequences, enabling the otic or more foreign protein expression cassettes to integrate into tile rBV DNA back bone. In some embodiments, the iB V genome comprises a rBV backbone comprising a foreign protein expression cassette encoding at least one AAV capsid protein.

P019] The disclosure also provides an insect cell comprising a recombinant bacuiovirus

(rBV) vector or particle comprising: a rBV genome: and at least one bacuioviral capsid protein. The rBV genome comprises: an rBV DMA backbone comprising; a chitinase gene; a deletion of the v-catk gene; an a DMA fragment enabling integration of one or more foreign protein expression cassettes into the backbone, such that the one or more foreign protein or proteins expressed m an insect cell are less degraded than they are when expressed from a rBV backbone without the deletion. The foreign protein expression cassette comprises: at least one foreign protein gene; an insect cell promoter opefabiy linked to the at least one foreign gene; and two DNA sequences, enabling the foreign protein expression cassette to integrate into the rBV ITNA backbone.

10020} In some embodiments, the insect cell is an Si*?, Sf2 ! , S2, Tr hopliisia ni, B4a, or

BTI-TK-5B1-4 cell. In particular embodiments, the Insect cell further comprises at least one foreign protein expressed train the foreign protein expression cassette in the rBY backbone of th rBV genome of the rBV vector or particle, and in certain embodiments, the at least one foreign protein is ai least one AAV capsid protein,

}0021| Also provided herein is an insect cell comprising a recombinant baculovirus vector or particle, comprising: a rBV genome: and at least one bacuioviral capsid protein. The rBV genome comprises: an rBV O A backbone comprising: a ehitinase gene; ft deletion of the v-cath gene; a selsction marker gene integrated into the cath-v deletion; tmd a DM A fragment enabling integration of one or more foreign protein expression cassettes into the backbone, such that the one or more foreign proteins expressed in an insect cell are less degraded than they arc whe expressed from a rBV backbone without the deletion. The foreign protein expression cassete comprises: at least one foreign protein gene; an insect cell promoter opembly linked to the a t least one Foreign gene; and two ^" DNA sequences, enabling die foreign protein expression cassette to integrate into the rBV DMA backbone,

(00:221 lit some embodiments, the insect cell is an S£9, SO1. S2, Triehop!usia ni, £4a, or

BTI-TN-SB1-4 cell In particular embodiments, the insect cell further comprises at least one foreign protein expressed from the foreign protein expression cassette in the r V backbone of the rB V genome of the rBV vector or particle, and in certain embodiments, the at least one foreign protein is at least one AAV capsid protein. 1110231 In another aspect, tire disclosure provides a heterologous expression system comprising: an rBV vector or particle; and an insect ceil. The rBV vector or particle comprises; an rBV genome; and at least one baeulovimi capsid protein, the rB V genome comprising: an rBV DNA backbone comprising: a chitinase gene; a deletion of the y~cath gene; and a DMA fragment enabling integration of one or more foreign protein expression cassettes into the backbone, such that the one or more foreign protein or proteins expressed in the insect cell are less egraded than they are when expressed from the rB V backbone without th deletion; and a foreign protein expression cassette, the foreign protein expression cassette comprising: at least one foreign protein gene; an msect cell promoter operably linke to the at least on foreign gene; and tw DNA sequences, enabling the foreign protein expression cassette to integrate into the rBV DNA backbone The insect cell in the system is susceptible to infection, and capable of expressing the at least one foreign protein encoded, by the rBV backbone in the rBV vector or particle.

|0Q24f In some embodiments. rBV vector or particle comprises an rBV backbone comprising a foreign protein expression cassette, the foreign protein expression _: casset comprising a sequence encoding at least one AAV capsid protein. Ip some embodiments _* the insect cell is an Slfo S121, S2, Tridmplusia ni, B4a, or BTl~TN SBl-4 cell.

(0025] In yet another aspect, the disclosure provides a heterologous expression system comprising; an rBV vector or particle; and an insect cell. Ί he recombinant baculovims vector or particle comprises: an: rBV genome; and at least one bacuioviral capsid protein. The rBV genome comprises: an rBV DNA backbone comprising; a chitinasc gene; a deletion of the v-cath gene; a selection marker cassette integrate into the cath-v deletion; and DNA fragment enablin integration of one or more foreign protein expression cassettes into the backbone, such that the one or more foreign protein or protei ns expressed in the insect cell are less degraded than they are when expressed from a rBV backbon without the deletion. The foreign protein expression cassette comprises; at least one foreign protein gene; an insect cell promoter opetably linke to the at least one foreign gene; and two DN A sequences, enabling the foreign protein expression cassette to integrate into the rB V DN A backbone. The insect eel! Of the system is susceptible t infectio , and capable of expressing the at least one foreig protein encoded, by the rB V backbone in the rB vector or particle. 100:26! In some embodiments. rBV vector or particle comprises an rBV backbone comprising a foreig protein expression cassette, the foreign protein expression cassete comprising a sequence encoding at least one AAV capsid protein in sortie embodiments, the insect cell is an SO I , S2, Trichopiusia ti, E4a, or BTTT foBI-4 ceil. 271 The preseat dis osuire also provides a nomviscous insect cell lysate, comprising; the recombinant bacukwinis (rBV) genome; and at least one foreign protein encoded by the rBV genome and expressed in the lysate. Th rBV genome comprises; an rBV l)hA backbonecomprising: a ehitfoase gene; a deletion of the v-cath gene; and a DNA fragment enabling integral ton of one or more foreign protein expression cassetes info the backbone, such lhai the one or more foreign protein or proteins expressed in an insect cell are less degraded than they are when expressed from a rB V backbone without the deletion. The foreign protein expression cassette comprises; at least one foreign protein gene; an insect cell promoter operably linked to the at least one foreign gene; anti two DNA sequences, enabling the foreig protein expression cassette to integrate into the rBV DNA backbone.

(<H)28J In some embodiments, the at least one foreign protein encoded by the rB V genome is at least one AAV capsid protein. In some embodiment foe insect cell lysate is derived thorn an Sffo Sf21 , S2, Triehopiusia nt, K4a. or RTS-TN-5B1 -4 insect cell infected with the rBV genome.

|#O20[ In another aspect, thedisclosure provides a. non-viscous insect cell lysate, comprising; a recombinant baeuki virus (rBV) genome; and at least one foreign protein encoded by the rBV genome and expressed hi the lysate. The rBV genome comprises; an fBV D A backbone comprising: a ebstinase gene; a deletion of foe v~mth gene; a selection marker gene cassette integrated into the mth-v deletion; and a DNA fragment enabling integration of one or more foreign protein expression cassetes into the backbone, such that the one or more foreign proteins expresse in an insect cell are less degraded than they tire when expressed if tint a tB V ^: backbone without foe deletion. The foreign protein expression cassette comprises: at least one foreign protein gene; an insect cell promoter Operably linked to the at least one foreign: gene; and two A sequences, enabling the foreign protein expression cassette to integrate into the rBV DNA backbone. )003G] In some embodiments, the at least one foreign protein encoded by the rBV genome i at least one AAV capsid protein. In some embodiments, the insect cell lysate is derived from an SI , SI2 I, S3, Tridioptiiina ni, ii4a _< or BTI-TN-5B1-4 insect cell infected with the rBV genome, je031 1 In st ll another aspect, the present disclosure provides a method of producing a foreign protei n in an insect cell comprising: infecting the insect cell with a recombinant baculovims (rBV) vector or particle; culturing flic infected cell under conditions conducive for the expression of die a! least one foreign protein gene; and isolating the foreign protein particle comprising; a rBV genome; and at least one baculovira! capsid rotein. The rBV vector or particle comprises: an rB V DNA backbone comprising: a chitioase gene; a deletion of the v- cafk gene; and a DNA fragment enabling integration of one or more foreign protein expression cassettes into the backbone, such that the one or more foreign protei or proteins expressed in the insect cell are less degraded than they are when expresse from a rBV backbone without the deletion. The foreign protein expression cassette comprises: at least one foreign protein gene; an insect cell promoter operabty linked to the at least one foreign gene; and two DNA sequences, enabling the foreign protein expression cassette to integrate into the rBV DNA backbone.

10032 In some embodiments, the insect cell is lysed to isolate the foreign protein, in certain embodiments, the foreign protein is at least one fecfimbinant AAV capsid protein.

18G33J The disclosure also provides a recombinant AAV capsid protein produced by this method,

10034] In another aspect, the present disclosure provides a method of producing a foreign protein hi an insect cell, comprising: infecting the insect cell with a recombinant bacuiovirus (rB V) vector or particle; culturing the infected cell under conditions conducive for the expression of the at least one foreign protein gene; and! solating the foreign protein. The rBV vector or particle comprises; an rBV DNA backbone comprising: a cliifinase gene; a deletion of the v-cafh gene; a selection marker gene cassette integrated into the eath÷v deletion; anti a 0NA fragment enabling integration of one or more foreign protein expression cassettes into the backbone, such that the one or more foreign protein or proteins expressed in the msec† cell are less degraded than they axe when expressed from a rBV backbone without the deletion. Tile foreign protein expression cassette comprises: at least one foreign protein gene: an insect cell promoter operably linked to the at least one foreign gene; and two DNA sequences, enabling the foreign protein expression cassette to integrate into the rBV DNA backbone.

1 35} In some embodiments _* the insect ceil is lysed lo isolate the foreign protein. In certain embodiments, the foreign protein is at leas! one recombinant AAV capsid protein.

[0036] The disclosure also provides a recombinant AAV capsid protein produced by: this method.

DESCRIPTION OF THE DRAWING 037] The foregoing and other objects of the present disclosure, the various features thereof, as well as the disclosure itself m y he more fully understood front the following description., when read together with the accompanying drawings in which: are diagrammatic representations of the recombinant baculo virus (rBV)

DNA backbones or bacim s according to the disclosure showing the deletion of foe v-vitik gene between nucleotides 107,034 and 107,904 and its replacement with the CAT expression casset flanked by two FRTs an a green fluorescent protein (OFF) expression cassette. A, foreign protein expression cassete(s) can he integrated into the rDV DNA backbone through the Tn7 transposoh sequence; B, foreign protein expression cassettc(s) can be integrated into the rBV DNA backbone through homologous recombination;

[0039] FIG, 2 is a schematic representation of representative DNA junction sequences between the v-mtk and CAT and GFF expression cassettes in the Av~mth rBV backbone, where bases 51 - 1066 are the C AT expression cassete, 1067 - 3223 are the OFF expression cassete, and 1-50 and 3224- 3275 bases are the remaining v~ca h sequence, and where the sequence is set forth in SEQ ID NO: 1:2;

[0040] FIG, 3 is a diagrammatic representation of the design of an exemplary foreign protein expression cassette including an bisect polyhedrin promoter (polh), AAV Rep and Gap (foreign protein) genes, and a selection marker gene gentamicin (Genial, flanked by Tn:7R and Tn7L sites for integration of the cassette into the recombinant baculovinis v-cath rBV DNA backbone:;

|00411 FIG. 4 Is a schematic representation of foe DNA sequences of the foreign protein expression cassette described in FIG, 3, including a repre entati e polh insect promoter, and the Tu7L and Tn7R sites for integration of the foreign protei expression cassette into the recombinant haculovirus Av-cath rBV DNA backbone, and where the sequence is set forth in SEQ ID NO: 13;

I I (§0 2! FIG. 5A ---· 5D are a series of diagrammatic representations of as exemplary Av ow/? rBV genomes induding a selection marker CAT expression cassette and GFP expression cassette which have been inserted at the position of the v-e ih deletion, and further including generic foreign protein expression cassetes carrying a gerrtamydn selection marker gene (Genta) _; and foreign Gene 1 and Gene 2 (FIG 5 A ); carrying Genta, AAV Rep, and Cap AA genes (FIG. 5B,) carrying Genta, an AAV enome consisting of a lueiferase gene (FIG, 5C); and carrying Genta, and mammalian proteins (human antibody heavy chain and human antibody light chain) genes (FIG. 3¾ each of which have been inserted into bMGN 14272 bac id:

(0043] F IG. 6 is a flow chart showing the process of deleting v-cath and production of the AAV vectors in insect cells using the rBV system according to the disclosure;

(0044} FIG. 7 A. is a diagrammatic representation of integrating a foreign expression cassette into the A v-caih rBVI>K¾\ backbone hy homologous recombination;

(O045J ITG. 7B s a diagrammatic representation of integratin a foreign expression cassette into the Av-caik rBV DN.4 backbone by trassposase;

(00461 FIG, 8 is a graphic representation of the titer of WT -rBVs and A v~catk rBV comprising the Cap6-rap expression cassettes, GFP expression cassette, o Cap2~7ni8-rcp expression cassettes respectively according to the disclosure;

(00471 FIG, 9 is a representation of an SDS-PAGE gel stained with Simply Blue showing AAV capsid proteins expressed from different recombinant haoulovit vectors carrying capsid VP I , VP2, and VP3 genes of different AAV serotypes with and without t e v- ccitk gene; 00 K( F IGS. 10A— 1 OF is series of representations of fl uoregrarns of l iEK~293

(mammalian) cells that had been transduced wtfli She same amount of AAV vectors comprising GFP expression cassette produced by rBVs with and without the v-mih gens where FIGS lOA - I OC show GPP-exprss sing AAV vectors produced by WT-rBVs, FIGS. lOD - FOP sho w GFP - expressing AAV vectors produced by v-anA-deleted rBV, where I0A and 10D are AAV7m8- GFP, 10B and 1 Oh are AA VS-GFP, and IOC and 1 OF arc AAV6-GFP;

[0049] FIG. j 1 is a diagrammatic- representation af&v-oath repombinant haeitlovims backbone containing the CAT expression cassette flanked by two FRTs only;

(00 0] FI G, 12 is a diagrammatic representation of the haeuiovirns backbone &v~m(k rBV after removal of the CAT expression cassette, leaving behind the GFP expression cassette and a single FRT site;

[0051] FIG. 13 is a diagrammatic representation of the Av-caih rBV backbone after removal of the CAT expression cassette, leaving one FRT sit behind;

[0052 ] FIG, 14 is a photograph ic representation of agarose gel electrophoresis image showing the removal of the CAT expression cassette from the & v-caik rBV backbone. A, smaller PCR fragments (2,345 bps) in lanes 1 - L L compared to lanes 12 and 13 (3,245 bps), indicating the removal of the CAT expression cassette from the A v-eaih rBV backbone containing both the CAT atid GTP expression cassetes, B, a 651-bp PCR fragment is shown in lanes 1, 5, an 7, indicating die correct fragment size after the removal of the CAT expression cassette from the v*cath rBV backbone with only one FRT site left behind;

10053] FIG. 15 is a schematic representation of a DNA sequencing analysis showing the removal of the C AT expression cassette from (A; SE0 ID NO; 14) the Av-eniVrBV backbone containing both the CAT and the GFP expression cassettes, and (B; SBQ ID NO: 15 ) the Av-cai rBV backbone containing only the CAT expression cassette; and

[0054] FIG. 16A— Ί 6D are a series of diagrammatic representations of an exemplary

&v~catk rBV genomes after removal of the CAT expression cassete and only ope FRT site left at the position of the v-cath deletion, and further including genetic foreign protein expression cassetes carrying a gentamydn selection marker gene (Genta), and foreign Gene i and Gene 2 (FIG i 6A); carrying Geiita, AAV Rep, and Cap AAV genes (FIG. T6B,}; carrying Genta, an AAV genome consisting of a hiciferase gene (PIG. 16C); and carrying Genta, and mammalian proteins (human antibody heavy chain and human antibody light chain) genes (FIG. 160), each of which have been inserted into bjVLOI 14272 baemid.

DESCRIPTION OSSI The disclosures of these patents, patent applications, and ubMcatio in thei entireties are hereby incorporated by reference into this application in order to more folly describe the state of the ait as known to those skilled therein as of die date of the invention described and claime herein· The instant disclosure will govern in the instance that there is anyinOo isteney between the patents, patent applications, and publications and this disclosure·

P0$6| 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 thi disclosure belongs. The initial definition provided for a group or term herein applies to that group or term throughout the present specification individually or as part of another group, unless otherwise indicated.

1 0571 The term“haan id’ ^* refers to a shuttle vector that can he propagated in both E, li arid insect ceils, A Av~cath buemid is a baemid having a deletion in. the i^cathepsiii genb.

{0058] The term ^recombinant baculovinis (rBV) DNA backbone” refers to a hacmid comprising a haciuld virus genome as described by Luckow et al ( 1903) that contains a bacterial origin of replication, an antibiotic resistant; gene and the mini-ait Tn7 site enabling the integration of an expression cassete into the backbone, and a cathcpsin gene,

100591 A Av~caih rBV backbone or Av~caih DNA /backbone is a baemid having a deletion in the v-eaf epsm gene and into which foreign gene cassettes including viral and/or mammalian genes can be inserted. The terms‘Dn-ewbV and“a deletion in the v-ceth (or cathepsin) gene” are used interchangeably herein. lOOhO] The term ^‘ ‘recombinant baculovims (rBV) genome” is used herein to ean a b oyirus DNA genome inclu ing at least one expression cassette encoding at feast one foreign protein. When the rBV genome includes a deleted v-cath gene, it is referred to as“Dn - onfe-rRV genome”. {0061) Ail rB V vector refers to a recombinat t baculovirus earrjdtig a rB V genome and encased withiii tlie hacukmras capsid and which is capable of infecting an insect cell

{0062) A " iral particle” refers to a biological entity comprising a shell formed by the expression and operative assembly within a cell, of capsid proteins, and genetic information in the form uf R A or DNA.

100631 A“selection marker gene” encompasses those genes that encode a selection marker protein useful for identifying or selecting an E, coti cell that has been successfully transformed by the baemul and for identifying and selecting an insect or mammali cell successfully infected by the fBV such as, but not limited to, a colorimetric protein or an

antibiotic-resistance protei n.

(006 | A“selection marker gene cassette” is a DNA sequence that encodes a non-native selection marker gene openibly linked to m E coH or insect promoter and comprising two insertion sequences which has enabled the integration of the cassette into the DNA backbone,

{0065) As used herein, the term‘"foreign protein” refers t a protein not encoded by a wild type baculovirus genome, Such proteins include, hut are not. limited to, non-insect proteins such as viral proteins and mammalian proteins,

10066) A“foreign protein expression cassette” is a DNA sequence encoding at least one non-bacutovirai protein such as a viral and/or mammalian protein, operabiy linked to an insect promoter enabling expression in an insect ceil, and may further comprise a DNA sequence operabiy linked to a mammalian gene promoter enabling expression in a mammalian cell. The foreign gene expression cassete may further link to a selection marker gene and insertion sequences enabling integration of the foreign gene ex ression cassette into the recombinant bar ulo virus DNA backbone.

{0067] L“donor piasinki” is a DNA vector or plasmid that has the foreign protein expression cassette flanked by recombination elements such as trail spo sons which can be use to transfer the foreign protein expression cassette to the bacmid t /generate the recombinant baeulovirus frBV) genome.

068| The present disclosure relates to a recombinant baeuiovirus (tBV) expression system for the production of foreign heterologous proteins, includi ng mammalian proteins in insect cells and which are useful for gene therapy. Tins system comprises a recombinant baeufoviius genome with a deletion in the cai e/mn gene iAv- wi M BVj into which foreign gene cassettes can be integrated, and an insect cell that can be infected by the Av _^ mih-rBY, and in which the foreign proteins anchor v iral vectors or particles are expressed or produced. j(Ml69j Insect cells infected by rBV with chirt se A arid v‘-etrtfepsin deletion are commonly used for expression of rceombinant proteins, particular iy AAV capsid proteins (Kaba, Salcedo et al. 2004; Galibett, Sav et ah 2018), However, the deletion of both chi.4 and v-eatk results in a gelatinous lysate due to the absence of chitinase A which cleaves the chitm- rich membrane of insect bells, Isolation of proteins from this viscous lysate is decreased owing gelatinous nature of the lysate, 0070 j The present syste unexpectedly enables the efficient production of foreign proteins of interest _; , and viral vectors and particles, without degradation and in an amount and infectivity level sufficient to be useful for therapeutic purposes. Relative to systems using infection of insect cells ith rBV having both a ehitmaxe A gene deletion and: a e-offiftepsin gene deletion, use of thepresent system rBV leads to greater AAV yields and greater structural integrity of the AAV capsid, especially in certain AAV mutants. This system also enables the direct expression of mammalian genes in an insect cell.

A v -c a ΐίi - B c i i 1 o v r u ¾ Backbone jW7 IJ A baeulovirus PHA- backbone according to the disclosure comprises a deletion of the &ih psin g ne. One Av ath DfSiA backbone according: to the diseiosure is show in FIG 1. The deletion is between nucleotides 107.034 and i 07,904 based on GenBank ID NC_i)01623. In one nohlrmiting example shown in ITG. i A, the Av-eath- DNA backbone includes the nimTat In? site that enables the insertion of one or more foreign gene cassettes for the expression of foreign proteins and nucleic acids of interest. In another example showing in FIG, IB, die AwoobVrBV DNA backboue/s DNA fragments from nucleotides 3272 to 451.8, and 5270 to 6689 based on GenBank ID 510 001623 were cloned into the pBacPAll shuttle plasmid to flank the one or more foreign gene cassettes such that the one or more foreign gene cassettes can be inserted into the Dn-trih-fBV DK A backbone through homologous

recombination.

10072] In some rBV backbones, a selection marker cassette is integrated into the Av~ cath deletion. For example, the v-caih deletion can be replaced with a chloramphenicol (CAT) selection marker expression cassette (GAT promoter- CAT ORF-polyA) Banked by two FRTs (see FIG, 11), Alternatively, In FIG IB, the Av-caih deletio has been replaced with a CAT selection marker expression cassette Hanked by two FRTs and a selection marker, green fluorescent protein (OFF) expression cassette (CMV promoter-GFP-WPRE-pQl ) The latter expression marker selection cassette is -useful for tracking successful infection into an insect; cell The cassette alternatively may include genes encoding other selection markers such as other colorimetric, fluorescent, of ehem ilum 1 nescent marker protei ns. Useful fluorescent marker proteins include, but arc not limited to, red fluorescent protoin, yellow fluorescent protein, bine fluorescent protein, and fudferase. Useful colorimetric marker proteins include, but are not limited to Uc fl-galaudositte antiSecreted embryonic alkaline phosphatase (SE APR Useflsl antibiotic resistance genes are also acceptable selection marker. Such genes include, but are not limited to, a kanamycin-resls ant gene, an ampiciMin-resistant gene, a tetracycline- resistant gene, a gentamicin-resistant gene, a blasticidm -resistant gene, or a chloramphenicol- resistant gene.

[00731 Another representative Av-caik rBV DMA backbones is shown in FIG. 13, This backbone does not include a selection marker gene expression cassette. It can be created from &v-mlh rBV KA backbone containing the CAT expression; cassette as depleted m FIG, IT through genomic engineering With the FLP-FRT recombination technolog that can remove the CAT expression cassette between the FRT sites, leaving only one FFLT site in the D Vrcath rBV DMA backbone.

[00741 The rBV Av-caih DN A backbone according to the disclosure also comprises a ehitinase gene (at positions 105,282 to 106,937 in FIGS, I , 1 1, 12, and 13. In addition, the backbone comprises a DMA fragment enabling integration of one or more foreign protein expression cassettes into the backbone. Useful examples of this fragment include, but are not limited to, the Tn7 transposou fragment, For example, in the rBV DNA backbone shown in FIG I A, this fragment is located within the LacZ coding sequence between the kanamydn gene and imrni-F replication sequence in the bMON 14272 rBV DNA backbone.

A v- Backbone Synthesis

10075] The Av caih backbone can be created from a bacraid comprising the WT baeulovi s genome (AcMNPV ( C 001623) into which the composite fragment (Kan LaeZi-minfratt Tn7 mini-E replication) is inserted into the polyhedriil region as depicted in bMON 14272, (see· EXAMPLE 2) or synthesized de now.

10076] If starting from the baemid, the CAT selection marker expression cassette flanked by two fljppasc recognition targets (FRXs) can be PCR-amplifted with primers 2846 (T’-TAATAA TGACTOCAGTAGACG-CAAGTTCGTTTCTGATACCACAGGCGTTT CCATATG AATATCCTCCTTA-3 ⁵ ) (SEQ ID O 1) and 6281

(A~ ATAACTAGTCAATAATCAATGTCGTGTAGGCTGGAGCTGCTTCGAAG’) (SEQ ID NO:2) and plasmid pKD3 as template. The GFP (or other selection marker) expression cassette ca be PCR-ampiified with primers 5701

(5’ -GACA ITGATfAriG ACTAG lTA'n AAl AtiT-3’} (SEQ ID NO:3) and 6282

(5 ' TJAACAAAATTTTGITTTATTTGTTTGTGTACGGCGTTGIAAACAGCGCGGT

T AGATCC AGACATGATA AGAT-T’) (SEQ I D NO‘4) and plasmid V376 as template. The two PCR fragments then can be joined together to form a larger PGR fragment with primers 6298 (5 ^: -TAATA ATGACTGCAGTAG ACGCAA-3’) (SEQ ID NOG) and 629

(SAGAACAAAATTTTGCTTTATTTGTTTGTGTAG^) (SEQ ID NO: 6) and the two PCR fragments as templates. This large PCR fragment can be recombined into the v-catk region between nucleotides 107,034 and 107,904 to disrupt the v-cetih gene via the lambda red system (Datseiiko and W anner 2000; Thomason, Sawitzke et til., 2014), The j unction sequence between CAT expression and GFP expression cassettes and remaining v-cath is shown in FIG. 2,

[0077} The A vcaih DNA backbone without a selection marker gene cassette can be created from a bacmid, for example bMON 14272 , or synthesized de novo. If starting from the bac id, the CAT selection marker expression cassette flanked by two flippase recognition targets (PRTs) can be PCR-ampltfled with primers 2845

(5 *- GAAC AA AATTTTGTTTTATTTGTTTGTGTACGGCCJTTGTAAAGAGCG CGGTT GTG ^' T AGGC TGGAGCTGCT-3 ^’ ) (SEC? ID NO;7) and 2846

(S^TAATAAATGACTGGAGTAGACGGAAGTTCGTTTCTCATACCACAG GCGTT TCCATATGAATATCCTCCTTA-3’) (SEQ ID NO: 1) and plasmid pKD3 as template. This PCR fragment con.tai.nmg the CAT expression cassette flanked by two FRTs can be recombined into the v-eatk region between nucleotides 107,034 and 107,904 to disrupt the v-caih gene via the lambda red system (Datsenko and Wanner 2000; Thomason, Sa itzke et a! .,2014). After selection of the bacmid DNA and confirmation of the catkepsin deletion, the CAT expression cassette can be removed with the FLP-FRT recombination technology, leaving only one FRT site in tlie bacmid as shown in FIG. 13,

Av-cath rBV Genome

10078} The rBV genome according to the disclosure is capable of replic ting in an E. colt cell and in an insect cell it comprises a A v-cath DNA backbone as described above, and a foreign protein expression cassette integrated in die Av-cath rBV genome. The foreign protei expression cassette includes a gene or genes enc ding foreign proteins of interest to be expressed in an insect cells, as well as a gene or genes encoding other proteins of interest to be expressed in mammalian cells . Useful genes encoding foreign proteins of interest for expression in insect ceils include, but are not limited to, vital proteins and/or mammalian proteins.

[0079] Useful viral proteins to be expressed ca form the structural part or capsid of a vector carrying a mammalian gene of interest and which is del iverable to mammalian cells. For example, the foreign protein expression cassette can include genes encoding AAV viral proteins, e,g., Rep and capsid: (Cap) proteins (FIG. SB). Proteins of other viruses useful in gene therapy methods include, but are not limited to, hexpn, penton complex., liber proteins from dsovirus, matrix, capsid, nucieocapsid proteins from retrovirus such: as, but not limited to, Ipstiviras, VP5, VP23, VF19G, VP P, and capsid-vertex-specifie component proteins from Herpes simplex vi s (HSV). and the major Ypt protein from SV40,

|00 t>] Useful mammalian proteins that can be directly expressed in insect cells include, but are not limited to, human immunoglobulins, human serum mlbumi , erythropdietiroalpha, and Factor VHI

|00iil ^: | The foreign protei cassette also includes control elements including, but not limited to, an insect cell promoter which enables expression of operably linked genes in an insect cell. Useful insect promoters include, but are not limited to, a polyhedron (polh), pl 0, O IE2 or p6.9 insect promoter. If the cassette includes mammalian genes t be expressed in a mammalian cells, promoter enabling expression of these mammalian genes in the mammalian cell will be opefably linked to that gene. Useful mammalian promoters include, but are not limited to, CMV, SV40, pGK, El la, syaapsin _» chicken beta iictin, and CamKTl promoter, etc,

[0082] Tlic foreign protein expression cassette may also Link to one or more additional selection marker gene. This marker gene is different than the selection marker gene in the selection marker expression cassette (if it is present in the rBV backbone) as described above which is expressed upon infection of the insect ceil.

I0083J The foreign protein expression cassette is flanked by transposable DNA elements enabling if to be integrate into the rBV UNA backbone at specific nucleic acid sites or locations. Useful transposable DNA element include, but are not limited to, To7L and Tn7R (FLU. I A), Alternatively, the foreign protein expression cassette can be flanked by sequences homologous to the rBV genome, for example the sequences between 3,272 and 4,518, and between 5,270 and 6,689, which enable it to be integrated into the rBV DNA backbone via homologous recombination mechanism as shown in PIG. I B.

[0084] As shown in FIG. 6, Integration of the cassette into the baculovixus backbone can be accomplished by transformation of a donor plasmid fe.gr., pPastBac-T). The donor plasmid comprises one or more foreign protein expression cassettes, operably linked to

2 ! appropriate promoter*, enhancer and polya ylation signal as well as a bacterial selection minkcr gene and promoter The transposase expressed by the helper plasmid catal zes the transpositio of Tn7L and Tn7R which flank the foreign protein expression cassettes at specific sites within the t nt-att n7 region of the bacmid, thus incorporating the foreign expression cassettes into the bacmid. Alternatively, die foreign protein expression cassettes can he inserted into the appropriate region of the recombinant haciilovi ms backbone by means of other methods such as but not limite to homologous .recombination using a donor plasmid that: contains homologous sequences of the rBV, which flank the foreign protein expression casse ttes as illustrated in FIG, IB,

10085] A diagram of an exemplary generic rBV genome with a v-c ik deletion/CAT and

OFF selection marker expression cassette insertion and the additional insertion of two foreign protein cassettes are shows in FIG. 5A. FIG. 5B shows the rB V genome with the Av-eathdeletion and insertion of AAV Rep and Cap foreign protein expression cassetes, FIG. 5C shows the rB V genome with the Av-cpiA delefion AAV. gentamyein. and luciierase foreign protein expression cassettes insertion. FIG. 5D shows the rBV genome with the L v-eath deletion and insertion of a gcntarayem/marnmaltan protein expressi on cassettes insertion encoding human antibody light and heavy chains. Alternatively, t e rBV genome with a v-tmb delctiun/withoui CAT and GFP selection marker expression cassete insertion an the additional insertion of two foreign protein cassettes are shown in FIG. USA. FIG. 16B shows the rBV genome with the άn-calh deletion and insertion. of AAV Rep and Cap foreign protein expression cassettes. FIG, 16C shows the rBV genome with the A v-cath deletion /AAV, gentamyein, and Incifcrasc foreign protein expression cassettes insertion FIG. I6,D shows the rBV genome with the A v mlh deletion and insertion of a gentamyein/manunaiian protein expression cassettes insertion encoding human anti hotly l ight and heavy chains.

Cell Culture

10086] Cells that can be infected by the rBV vector or transformed by bacniid include insect cells or prokaryotic cells such as ,E vil Useful £. call cells include, hut are not limited to, Top 10, D.115a, D ll QB, TGI, B 23473, BW23474 MWW3, Mwow, and BUT l seiu! msect cells that can be infected by tile rBV vector include, but are not limited to, SfA Sf21. Express SfR and $2 cells from the Fail Army worm (Spmioptemfi-ugiper a). or BT1-TN-5B1 -4 (High Five ceils) from the cabbage luuper Tnchoplusia ni {Lepidoptera}. D, melmog stp r, and oilier cell lines. These cells are commercially available from a number of sources (£?,¾ ,

ThermoFisher Scientific, ATCC. and Expression Systems). Insect cells are cultured in a medium conducive for maintenance and growth, such as, hut not limited to Gjbco insect media; E piSf CD Medium, Sf-90Q TIT SFM, Express Five SFM, or SF-900 II SFM

(ThcrmaFisher Seienttfic), ES ^: F921 and ESFAF (Expression Systems),

FBV Infection

[008?] fBV infects insect; cells upon contact under conditions conducive from the virus to enter the cell tygv, by culturing the contacted cells at about div'C for about three days in a medium conducive for expression of the foreign proteins, e,g,, in Gibeo insect media (ExpiSf CD Medium, Sf-900 III SFM, Express Five SFM, or SF-900 ITS M (ThenaoFisher Scientific), ESF921 or ESF AF media (Expression Systems), Successful infection can be monitored e& , by expression of a visuallydetectable selection marker protein, or the expression of the gene for which had been incorporated into the rBV genome.

Foreign Protein Expression an Isolation

[9088] Foreign protei ns including those whi ch are the structural part of viral vectors carrying mammalian genes, or directly expressed from mammalian genes can be obtained from infected insect cells by lysing the cells and isolating the proteins from the lysate. Lysing can be accomplished with physical force ( g, with a French Press or sonieation), detergent-containing lysis buffer, or enzymatic digestion of the cell matrix with, e,g., ddtmase that is naturally expressed by the baaikwiras genome, The expressed foreign: proteins or produced viral particles can be isolat ed, for example, by chromatographic or electrophoresis methods or by centrifugation, e.g., on cesium chloride gradients.

[0090] These isolate and purified proteins can then be used, eg,, for therapeutic purposes or as research reagents. If the foreign protein is part of a viral yeetop that carries mammalian genes, the viral vector is isolated and then can be used to infect mammalian ceils, e.g., for gene therapy.

Effect of rite? Deletion on Foreign Protein Expression i#091 [ To demonstrate that deletion f the v-caih gene from the bacuSovirus genome ad no efibcl on baeoloviros replication _s the replication of wild type rBV was compared with the replication of the Ay-«i£/j-rBV according to the disclosure. Both rBVs carrying the same foreign (AAV capsid and rep or GBP) genes were used to infect insect (Sf9) cells, WT baculovirus and n-c th deletion mutant rB V tilers were then determined to be similar, demonstrating that v-cath deletion lias no negative impact on virus production (FIG. 8).

100 2| To demonstrate that the foreign proteins expressed from A v-catk rBV are not degraded, foreign protein expression m.Av-mth rBV fected cells was compared with protein expression in WT-rBY-iftfected cells, The resulting synthesized AAV vectors w¾re then purified from the cell lysates. After heating both types of AAV particles _» . _: their capsid proteins were examined by SDS-P AGR

{0093J The results shown i n F I G. 9 demonstrate that del etion of the v-mth gene decreased capsid protein degradation. AAV7m8 was severely degraded when produced with WT-rBVs, in contrast to the AAV7m8 capsids produced with Av-en/A-rBVs, where no degradation was seen (compare lane 2 with lane 6). There was only minor degradation to the A.AV8 (lane 3) and AA.V6 (lane 4) capsid proteins.

{00941 To demonstrate that Av~ea†h rBVs can produce higher AAV yields than WT- rBVs, AAV 7rn8-lueiferase and AA Vphpbduciibrase vectors were produced in SI9 cells infected with breath rBVs and WT-rBVs, respectively, When preparing cell lysates, the protease inhibitor Leupeptin was added to the lysis buffer for W T-rB V infected lysates to prevent degradation so that AAV production yield eoiild he preserved. No protease inhibitor was added to Av-eoA/ TBV-infeeted. lysates. After purification, the AAV vectors were quantified. The results are shown in Table 1. Table L Comparison of AAV Production Yields Between Av-cath rBVs and WT-rBVs

Lot no. Type of Type of AAV AAV production yield Folds of

rBV (yg/L) difference

{0095j These results show that foreign protein expression in A y- at rBV-tmnsdueed ceils was 3x to 4x greater than the saine foreign protein expression in WT-rBV -transduced cells,

(0096 j it was also dtfemimed that AAV vectors produced with Av-cath rBVs relative to those produced with WT-rBVs had greater infectiyity in mammalian cells. Testing was done in HEK-293 cells using AAV vectors isolate from insect cells infected with either the WT-rBVs or the deletion mutants, OFF expression as recorded. The results shown in PIGS. 10A - 1 F demonstrate that AA vectors produced with WT-rBVs (FIGS. I DA - I OC) have lower iofecti vity than those produce "with &v-cath rBVs (FIGS. 1 OD 1 OF).

(00971 Reference will now be made to specific examples illustrating tire disclosure. It is to be understood that the examples are provided to illustrate exemplary embodiments and that no limitation to the scope of the disclosure is intended thereby.

EXAMPLES

EXAMPLE 1

insect Cell Culture

{0098| Sf9 cells (Expression Systems, Davis. CA) were cultured in Corning storage bottles at SS^C in ESF921 or E$F AF media (Expression Systems) supplemented with 100 nmts/rhL penicillin and 100 pg/mL streptomycin (IlyClone, Logan, tIT). The cells were split 1 :4 once the cell density reaches about 8 1 (ft cells/ rnE for maintenance.

EXAMPLE 2

Deletion of v-eath Gene rom Baenlovirus Backbone

|0099j The protocol of lambda red system (Thomason, Sawitzke et a!., 2014) was used to perform the deletion. Briefly, a 1 , 1 kB fragment containing rive chloramphenicol

aeetyltmnsferase (CAT) expression cassette flanked by two FRT$ (FIG, 2, bases 51— 1 066) was ECR-anspilfted with primers 2846 (SEQ ID NO; I) and 6281 (SEQ ID O:2) and plasmid pKD3 (The QD1K, Oakland, ^; GA) as a template. A 2/2 Kb fragment containing the CEP expression cassette (FIG. 2, base 1067 - 3223) was PCR-ampitfied with primers 5701 (SEQ ID MQ:3) and 6282 (SEQ ID NO:4) andV3?6 template. After gel purification, both PCR fragments were Joined to form a 3275-bp PCR fragment With primers 6298 (SEQ ID O:5) an 6299 (SEQ ID NO:6) The PCR fragment was digested with restriction enzyme Dp.nl (New England Biolabs, Ipswich, MA) to remove contaminating plasmid template. Then plasmid pKD46 containing the re tecirmhiiiase (Tile ODIN) was electroporated into tire DH I OBae-conipetent cells

(ThermoFisher Scientific ) to obtain Dill OBac colonies containing the red recombinase, One of the colonies was induced with 0,035% L-( H-arabinose (Sigma- Aldrich, St. Louis, MO) to express the recombinase After induction for 45 min at 37°C with gentle shaking, the DHIOBae- competent cells containing the red recombinase were electroporated with the 3275-bp CAT- GFP PCR fragment and incubated for another 3 hours for recombination to occiir. The electroporated DH1 OBac-red cells were cultured overnight. fOQieO] Colonies containing the haemid with v _* wtfi deletion were verified by DNA sequencing analysis and designated as DII iOBac-Av-cufo, One of these colonies was chosen to prepare competent ceils which were used for generation of recombinant baoiiloyiriis without v- cath. EXAMPLE 3

Recombinant Baciilovims Generation

l OIOi 1 Recombinant biiuulovirus containin the genes of interest were generated usin recombinant baculo irus shuttle vectors (bacni s) that can recombine with a donor plasmi according to manufacturer’s protocol (Invitrogen, Carlsbad,€ A), Briefly, the donor plasmids were diluted in sterile T£ buffer (10 iiM Ifis-HCL. 1 mM: EDTA, pH: 8.0) to a eoiicentratioD of 2 ng/ pL, and 2 mG, of the diluted plasmid DMA was used to transform 20 m ^: E of OHlOBae-wi ld type (\v†)- or DHlOBac- Av ni/A-competerit ceils. After 2 days of incubation on the LR-agar plates at 37 ^C C, white colonies were picked and mmiprep bactnid DNAs prepared according to manufacturer ^' s protocol (Titvitrogen). f OI 021 The ininiprep haemid DM As were then used to transfect S19 cells to generate recombinant baculowiruses according to manufectorer’ s protocol (Mvitrogen) with

modifications Briefly, 5gg miaiprep bactnid DNA and 5m1 GenJet reagent (SignaGene Labs, Rockville, Mb) were each diluted in 100 mI of ESP AF media (Ex pressiors Systems) in sterile 1.5 ml. mierofugc tubes. The diluted GenJet reagent was transferred to the diluted baenrid DMA tube and mix by gentle pipette up and down for 3 times. After incubation at room temperature lor about 30 min, 0.8 mL ESF AP media was added to the GenJet-taacimd mixture and mised by pipette up and own 3 times. Sfo cells were plated on 6-well plate at density of 1,5 A 10° cells/ well in 2 tnL ESF AF edia and incubated at 28°C in an incubator for about 30 rain to attach. The media from each well was remove and the GenJet-baemid mixture was then added. After Incubation at 28 C in the incubator overnight, 1 mL of ESF AF media was added and the plate was incubated at 28 C tor a total of 4 days for recombinant baeu!oviras to be generated. The recombinant bacidoviruscs in the media were collected and stored at 4 ^C G under dark. j©0l 03) The recombinant haculovt ruses generated from PH i08ac-wi and Dill OBac-Av- c<iih were designated as WT -rBY, and &.v-mih rBV, respecti vely. EXAMPLE 4

Impact o Deletion on rBV Replication

[410104! To determine if deletion of die v-cafh gene affected replication of bacu lb virus, three pairs of WT-rBV a hd &v-eaik rBV were used. The first pair WT~rB V -Cap 6-Rep and &v- i//i-.rB V- ap6-Re each carries AAV6 capsid gene encoding V.P I , VP2, and VP3 and AAV2 rep gene encoding re 78 and rep52. The second pair WTfoBV -GTRahd Awc«i¾ rBV-GFP each carries CTFP gene encoding the green fluorescent protein. The third pair WT-rBV-Cfap7m8-Rep and Av-cath rBV-Cap7m8-Rcp each carries AAV 7ni8 capsid gene encoding VPI , VP2. and VP3 and AAV2 rep gene encoding rep?8 and rep52.

[00! 05 j All the rBVs generated wen? used to infect Sf9 cells for amplification, Briefly, 1 SBL of each rBV was added to 200 ml, of Sf9 cell at density of 2 x 10 ⁶ ceilsanL i a. Corning culture brittle, respectively, and the rBV amplification was carried out for 3 days at 28°C and 180 rpra in a shaker incubator (New Brunswick, Hauppauge, N Y). The supernatants were harvested by centrifugation at 2.000 t m for 10 min to remove the cell pellets. The rBV titers in the supernatant were determined: by the quantitative polymerase chain reaction ( PCR) method as described in EXAMPLE 5.

EXAMPLE 5

Quantification of rBV

{00106] o determine the titers of recombinant bacuio viruses. a specific QPCR method for rBV titration developed in Virovek was employed. Briefly, 50 mΐ rBV supernatant was mixed with 50 pL 0.2% SDS solution and heated at 95 °C for 30 min to release the rBV DMA. The rB V DMA was diluted 1 : 100 with QPCR dilution buffer (10 pg iL yeas iRNA (Sigma Aldrich, _: Saint Louis, MO):, 0.01% Twe SO, 10 niM Tris-HCl (pH 8.0), 1 mM EDTA) and the copy numbers of rBV were determined with Chromo 4 Tour-Color Real-time Defection System (Bio- Rad, Hercules, CA) using primers corresponding to the : gentamicin gene

(3065: S’- ATTTGAt. TGGTCA(tGCiCCCr-3’d ( EQ ID NO:8) and 3066: 5 TGTTACGCAGCAGGGC AGTC-3’ (SliQ 11). NO:9)) and SYBR Green FOR Master Mix (ThermoFisher Scientific, Fremont, CA). One plaque forming unit (pin) was empirieally determined to contain average of 20 copies of xBV genomes.

EXAMPLE 6

AAV Vector Production and Purification

[001 (}7| Recombinant ImcnioYimses were sed to infect insect cell s to produce A A V vectors;. Briefly. 10 mol of recombinant haeufovinis containing AAV.Rep and Cap genes were eo-utfected with 5 mot of recombinant bacuiovims containing the GFP market gene flanked by A A V FTRs for 3 days at 21TC. Cell pellets were collected by centrifugation at 3000 tpm for 10 min. The cell pellets wer lysed in SF9 lysis buffer (50 M Tris-HCI, pH 7,8, 50 mM NaCt, 2 mM MgCi _¾ i% Sarkosyl, i% Triton XTOO, and 140 unifs/iiiL Benzonass nuclease {Sigma Aldrich) by sonicatidn. Cell debris was removed by centrifugation at 8,000 rpm for 20 min, The cleared lysates of about 23 m each wtne transfetred fo ultracleai centrifuge tubes lot SW2H rotor (Beckman Coulter, Brea, CA), followed by 10 mL of 1 32g¾c and 5 mL of 1 55 g/ee CsCl solutions and centri fuged at 28,000 rpm at 1 5 ^® C for about 20 hours. The AAV vector band was visualized with a beam light shining underneath and collected with a syringe needle. The collected AAV vectors were transferred into another centrifuge tube for a 70.1 ti rotor

(Beckman Coulter) which was then filled with 1.38 g/ce CsCl solution and sealed. After centrifugation at 65,000 rpm for about 20 hours, the AAV vector band was visualized with a beam: light shining underneath and collected with a syringe needle. The AAV vectors were buffer exchanged with PiMO desalting columns (GE Healthcare Bio-Sciences, Pittsburgh, FA), After filter sterilization, the AAV vectors were used for further experiments.

EXAMPLE 7

AAV Vector Quantification

100108] AAV vectors in crude lysates or in purified .form were quantified with QPCR according to protocol described by Aumhamme et at, (Hum. Gene Ther. eth. (2012) 23(1): 18-28) with modifications. Briefly, AAV samples were first diluted 1: 100 with QPCR dilution bu ffer and contaminating DN A was removed by incubating 10 mΐ diluted AAV with 1 m] (2 units) DNasel enzyme (New England Biolabs) in 39 mΐ DNasel digestion buffer (10 niM Tris- HC1, pH 8,0, 2.5 niM MgCfo Q.5 luM CaCb) at 37 ^'J C for 1 hour. The DNase 1 enzyme was inactivated by mixing with 50 pi of 200 niM EDTA and heating at 95X2 for 30 min, The treated A AV samples were further diluted 1 :200, and ID mί of each AAV sample was used in the Chmmo4 QPCR machine (Bio-Rad, Hercules, CA) to determine the copy numbers of AAV vector genome.

EXAMPLE 8

Preservation of Capsid Integrity in Av~cath AV Vectors

100109] AAV vectors were produced by co-infection of SB) cells with Av-cath tjBVs or WT-rBVand pofilied fey twu rounds of cesium chloride ultracentrifugatiorv as described in

EXAMPLE fo Equal apmmts (1 x It) ¹¹ vg) of purified AAV particles were heated at 95°C for 5 in. Capsid proteins were separated by SDS-PAGE and staine with a Simply Blue staining kit to determine the amount of degradation, if an , of the capsid proteins produced by each type of rBV.

EXAMPLE 9

infects vitv of rBV -Produced AAV Vectors

(001101 AA V vectors produced in Sf9 cells with A v cath rBVs or WT-rBVs were purified and quantified as described above in EXA PLE 7. These AAV vectors were used to transduce HEK- 293 cells for comparisufi of their infctivities The HEK-293 cells (ATCC- CRL-1573, anassas, VA) were cultured in DMEM media (Mediatech, Manassas, VA) supplemented with 100 units of FeuiciliiivSireptomycio (Corning, Coming, NY) with 10% FBS (Hyelone, Logan, UT) in Coming 12-well cell culture _· late in a C<¾ incubator at 37 C until about 70% confluent. The AAV samples were diluted each in 1 ml. of DMEM containing 20 pm etoposide (ATT. Scientific, San Diego, CA) but without FBS to obtain 3.0G-÷-9 vg/ml.. After the old media was removed from the plate, 0.5 inL of diluted AAV sample was adde to each well, and the plate was incubated in the C(¾ incubator at 3?°C overnight. The next morning, 0.3 ml, DMEM medium containing 20% FBS and 100 units of Penicillm-Streptomycln was added to each well, and the transduction was carried out fox 2 to 3 days, GET- expressing cells were recorded with the Nikon Eclipse TSIOU fluorescence microscope (Nikon instruments, Melville, N Y).

EXAMPLE 10

Expression of SV4Q Capsid Proteins in A two© rBV-Infected Insect Cells

[00111] Recombinant haculovirus carrying SV40 capsid genes was used to infect insect cells t express the SV40 capsid proteins. Briefly, 10 t ioi of the recombinant bacwlovirus were added to 300 ml, S© cells and incubated for 3 da ys a ! 28°C, Cell pellets were collected by centrifugation at 3000 rpm for LG min, The cell pellets were lysed in S 9 lysis buffer (50 mM Tris-HCl, pH 7.8, 50 mM NaCl, 2 mM gC , 1% Sarkosyi, 1% Triton X- llKJ, and 140 units/mL Benzonase nuclease (Sigma Aldrich) by son i cation. Cell debris was removed b centtifugation at 8,000 t tn for 20 min. The cleared lysate of about 23 mL was transferred to nltraelear centrifuge tube for SW28 rotor (Beckman Conker, Brea, C A), followed by I fl ml, of 132 g/ec and 5 mi, of 1.55 g cc GsCl solutions and centrifuged at 28,000 rpm at 15 ^a C for about 20 hours. The SV40 virus-like band was visualized with a beam light shining underneath andcollected ith » syringe needle. The collected SV40 virus-like particles were tiansferred into another centrifuge tube for a 70.1 ti rotor ( Beckman Coulter) which was then tilled with 138 g- ^' ee CsCt solution and sealed. After cenMfhgatioii at 65,000 rpm for about 20 hours, the S V40 vims-like particle hand was visualized with a beam light shining underneath and collected with a syringe needle. The SV40 vtms-ltke particles were buffer exchange with PD- 10 desalting columns (GE Healthcare Bio-Sciences, Pittsburgh, PA), After filter sterilization, the SV40 viru like articles were used for further experiments.

EXAMPLE 11

Expression of Human Antibody Heavy and Light Chains in άn-eatk rBV-Infeeted Insect

Celts

[00112] Recombinant cuJovims carrying die human antibody heavy chain nd light chain expression cassettes was used to infect S© cells for protein expression. Briefly, 10 moi of tBVs were used to Infect 300 ml, S© cells for 3 days at 28”C and both supernatant and cell pellet were harvested respectively. The cell pellet was lysed in the S© lysis buffer, as described

3 ! in EXAMPLE 6, and the cleared lysate was collected. Expressed human antibody in the supernatant and lysate were purified with protein-A agarose and analyzed by SDS-BAGE,

{00113{ Two versions of ea^e sm-deteted baculovirus DMA baclcbofles were constructed; one with li e CAT expression cassette flanked by tw FRTs and the other with the CAT expression cassete flanked by two Fill plus the OFF expression cassete integrated Into the eathepsin- deletion re gion,

{§0114j To remove the CAT expression cassette between FRT sites from the baeuloviras backbone, the following experiment was performed. Glycerol stocks of bacteria containing Dill 0Bae-Aea i were streak on an LB plate containing 10 jiig/niL tetracycline and 25 pg-mvL chloramphenicol and were grown overnight (ON) ai 37°C. The following evening a well· grown colony was picked and grown ON in 1 aiL LB media containing 10 pg/niL tetracycline and 25 pghnL chloramphenicol at 37 C with agitation, The following morning, 30 mL of the ON culture was diluted into 1 ,4 mL of LB media containing ID pghmL tetracycline and 25 pgTnL chioramphemea! and grown at 37"CTo an QD _& uo of between 0,3 0.5. The cell pellet was collected by centnftigatfori at 1 1 ,00(1 rpm for 30 see. After removing the supernatant, the cell pellet was put on ice and resuspen ded in 1 ml, ice-cold 1 0% glycerol . The cell pellet was centrifuged again at 1 1,000 ipni for 30 sec to remove most of the supernatant, leaving 20 - 30 pL in the tube to resuspend the ceil pellet. One pL (500 ng/pL) of plasmid pCP20, containing the FLP reeombimse (The ODIN, Oakland, CA ) was added to the resuspetided cells kepi on ice and mixed briefly. The cells were then transferred to a chilled electroporation cuvette

(Molecular Bioproducts, Inc,. Cat#5S HFl 1 , Fischer Scientific} and electroporated with the ‘'Bacteria” Setting on the RioRad MicmPulser machine (Hercules, Ca). After electroporation, the cells were added to 1 ml, LB media without antibiotics, and incubated at 3CFC lor 2 hr with agitation. One hundred jiL of the cel! solution was plated o an LB plate containing 100 p.gVnL ampieillm (Thermo Fisher Scientific, Waltham, MA), 50 pginL kai myem (Thermo Fisher Scientific, Waltham:, MA), nn 1 0 pg/rnL tetracycline (Thermo Fisher Scientific, Waltham, MA), and cultured at 30 ^C C ON, Eleven weil-yrown colonies were picked, streaked on. an LB plate without antibiotics, and cultured at 43 ^a C ON to xpress the reeombinase, which removed the chloramphenicol expression cassettes located between 2 FRT sites through recombination. The next morning. bacteria from each colony were removed with a pipette tip and resuspended in 20 pL cold Mill! Q-pnrif!ed (Miilipore Stgnm) water.

(00115] PCR reacti ons were performed to veri ty the removal of the DNA s qu ence between the 2 PRT sites using 2 pL resuspended bacteria from each colony. Forward primer 6298 (5’-TAATA AATGACTGCAGTAG ACGCAA-3 ^* ) (SEQ ID NO ; S), and reverse primer 6299 (5 ^, - GAACAAAATTTlOTTTTATTTGTTFGTGTA-3 ^, } (SIiQ ID NO; 6} were used to verity the removal of the CAT expression cassette from DHIORae-Av- //? containing the CAT expressio cassette flanked by two FRTs plus the GFP expression cassette. Forward primer 284? (5’-CTACGAGGGCATAATTGCGA-3’) (SEQ TD NO: 10} and reverse primer 2848 (3’ -GTTT GOT C ATGTAGTT A ACTTT G-3 * } (SEQ ID NO; 1 1 ) were used to verify the removal of the CAT expression cassette from D! IlOBac-A v-mih containing only the FRT franke CAT expression cassette, The PCR condition shown below in Table 2 were used.

Table 2

100116} After the PCR reactions, the amplifie PCR fragments were electrophoresed on a

1% agarose gel. As shown in FIG, 14A, for Dll I 0Bac~Av-eai¾ containing the CAT and the GFP expression cassettes, the PCR fragments from the 11 colonies have a fragment size of 2346 bps, whereas the control colonies #12, and #13 have a fragment size of 3276 bps, indicating that the CAT expression cassette (930 bps) ha been remove from colonies I— 1 1. DNA sequencing analysis further confirmed the removal of the CAT expression cassette, leaving the FRT

(minimal) sequence and the GFP expression cassette in the v cath deletion region (FIG, IS A), {001I7j For illi)Bae Avroa¾ containing only the CAT expression cassette flanked by two FRTs, thorn the 8 colonies that had undergone the removal process only 3 colonies (#1, #5, and #7) showe PCR amplification of a fragment si/e of 651 bps, indicating the removal of CAT expression cassette (FIG, 14B), DNA sequencing analysis farther confirmed the removal Of the CAT expression cassette leaving only the FRT equence in the y^cath deletion reg on (FIG _* 15B).

EQUIVALENTS

100118 Those skilled in the art will recognize, or be able to ascertain, using no mor than routiihe experimentation. numerous equivalents to the specific embodiments described

specifically herds. Such equivalents are intended to be encompassed in the scope of the following claims.