Directed evolution and in vitro panning of virus vectors
View Patent ↗The present invention provides methods of achieving directed evolution of viruses by in vivo screening or “panning” to identify viruses comprising scrambled AAV capsids having characteristics of interest, e.g., tropism profile and/or neutralization profile (e.g., ability to evade neutralizing antibodies). The invention also provides scrambled AAV capsids and virus particles comprising the same.
1. A nucleic acid encoding an AAV capsid, the nucleic acid comprising an AAV capsid coding sequence selected from the group consisting of:
(a) the nucleotide sequence of FIG. 6Q (HH67) (SEQ ID NO:55);
(b) a nucleotide sequence that is at least 98% identical to the nucleotide sequence of FIG. 6Q (HH67) (SEQ ID NO:55); and
(c) a nucleotide sequence that encodes the AAV capsid encoded by the nucleotide sequence of (a) but that differs from the nucleotide sequence of (a) due to the degeneracy of the genetic code.
2. The nucleic acid of claim 1 , wherein the nucleic acid is a plasmid, phage, viral vector, bacterial artificial chromosome (BAC), or yeast artificial chromosome (YAC).
3. The nucleic acid of claim 2 , wherein the nucleic acid is an AAV vector comprising the coding sequence.
4. The nucleic acid of claim 3 , wherein the nucleic acid further comprises an AAV Rep coding sequence.
5. A cell having the nucleic acid of claim 1 stably incorporated into its genome.
6. A virus particle comprising the nucleic acid of claim 1 .
7. The virus particle of claim 6 , wherein the virus particle is an AAV particle, an adenovirus particle, a herpesvirus particle, or a baculovirus particle.
8. An AAV capsid encoded by the nucleic acid of claim 1 .
9. The AAV capsid of claim 8 covalently linked, bound to, or encapsidating a compound selected from the group consisting of a DNA molecule, an RNA molecule, a polypeptide, a carbohydrate, a lipid, and a small organic molecule.
10. An AAV particle comprising:
an AAV vector genome; and
the AAV capsid of claim 8 , wherein the AAV capsid encapsidates the AAV vector genome.
11. The AAV particle of claim 10 , wherein the AAV vector genome comprises a heterologous nucleic acid.
12. The AAV particle of claim 11 , wherein the heterologous nucleic acid encodes an antisense RNA, microRNA or RNAi.
13. The AAV particle of claim 11 , wherein the heterologous nucleic acid encodes a polypeptide.
14. The AAV particle of claim 11 , wherein the heterologous nucleic acid encodes an immunogen.
15. The AAV particle of claim 11 , wherein the heterologous nucleic acid encodes a therapeutic polypeptide.
16. The AAV particle of claim 11 , wherein the heterologous nucleic acid encodes dystrophin, a mini-dystrophin, a micro-dystrophin, a laminin-α2, a mini-agrin, an α-sarcoglycan, a β-sarcoglycan, a γ-sarcoglycan, a δ-sarcoglycan, utrophin, Fukutin-related protein, myostatin pro-peptide, follistatin, dominant negative myostatin, IGF-1, a sarcoplasmic endoreticulum Ca 2+ -ATPase (SERCA2a), a β-adrenergic receptor kinase inhibitor (βARKct), phospholamban, PI3 kinase, Pim-1, POC-1α, SOD-1, SOD-2, EC-SOD, Kallikrein, HIF, thymosin-β4, mir-1, mir-133, mir-206, mir-208, inhibitor 1 of protein phosphatase 1, an anti-apoptotic factor, an angiogenic factor, insulin, Factor IX, Factor VIII, glucocerebrosidase, α-galactosidase A and/or lysosomal acid α glucosidase.
17. The AAV particle of claim 11 , wherein the heterologous nucleic acid encodes a reporter protein.
18. A pharmaceutical formulation comprising the nucleic acid of claim 1 in a pharmaceutically acceptable carrier.
19. A pharmaceutical formulation comprising the cell of claim 5 in a pharmaceutically acceptable carrier.
20. A pharmaceutical formulation comprising the virus particle of claim 6 in a pharmaceutically acceptable carrier.
21. A pharmaceutical formulation comprising the AAV capsid of claim 9 in a pharmaceutically acceptable carrier.
22. A pharmaceutical formulation comprising the AAV particle of claim 11 in a pharmaceutically acceptable carrier.
23. A method of producing a recombinant AAV particle comprising an AAV capsid, the method comprising:
providing a cell in vitro with a nucleic acid according to claim 1 , an AAV rep coding sequence, an AAV vector genome comprising a heterologous nucleic acid, and helper functions for generating a productive AAV infection; and
allowing assembly of the recombinant AAV particle comprising the AAV capsid and encapsidating the AAV vector genome.
24. A recombinant AAV particle produced by the method of claim 23 .
25. A method of delivering a heterologlys nucleic acid to a cell in vitro, the method comprising administering the AAV particle of claim 11 to the cell.
26. The method of claim 25 , wherein the cell is a liver cell.