IP Library Granted Patent US 10,294,281
Granted Patent B2
US 10,294,281 · App. 15/444,235 · Granted May 21, 2019

High-transduction-efficiency rAAV vectors, compositions, and methods of use

Inventors: Arun Srivastava (Gainesville, FL); George Vladimirovich Aslanidi (Gainesville, FL); Kim M. Van Vliet (Gainesville, FL); Mavis Agbandje-McKenna (Gainesville, FL)
Assignee: University of Florida Research Foundation, Incorporated
C07K14/005C12N15/86C12N2750/14122C12N2750/14143C12N2750/14145
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Quick Facts
Patent No.
US 10,294,281
App. No.
15/444,235
Granted
May 21, 2019
Kind
B2
Abstract

The present invention provides AAV capsid proteins comprising modification of one or a combination of the surface-exposed lysine, serine, threonine and/or tyrosine residues in the VP3 region. Also provided are rAAV virions comprising the AAV capsid proteins of the present invention, as well as nucleic acid molecules and rAAV vectors encoding the AAV capsid proteins of the present invention. Advantageously, the rAAV vectors and virions of the present invention have improved efficiency in transduction of a variety of cells, tissues and organs of interest, when compared to wild-type rAAV vectors and virions.

Claims (23)

1. An isolated nucleic acid molecule that encodes a non-naturally occuring AAV capsid protein comprising one or more of the following modified residues:

(a) a non-lysine amino acid residue at a position that corresponds to K258, K321, K459, K490, K507, K527, K572, K532, K544, K549, K556, K649, K655, K665, or K706 of the wild-type AAV2 capsid protein of SEQ ID NO:2;

(b) a non-lysine amino acid residue at a position that corresponds to K530, K547, or K569 of the wild-type AAV8 capsid protein of SEQ ID NO:8;

(c) a non-serine amino acid residue at a position that corresponds to S261, S264, S267, S276, S384, S458, S468, S492, S498, S578, S658, S662, S668, S707, or S721 of the wild-type AAV2 capsid protein of SEQ ID NO:2; and/or

(d) a non-threonine amino acid residue at a position that corresponds to T251, T329, T330, T454, T455, T503, T550, T592, T581, T597, T491, T671, T659, T660, T701, T713, or T716 of the wild-type AAV2 capsid protein of SEQ ID NO:2.

2. The isolated nucleic acid molecule of claim 1 , wherein the modified AAC capsid protein comprises a non-lysine amino acid residue at a position that corresponds to K258, K321, K459, K490, K507, K527, K572, K532, K544, K549, K556, K649, K655, K665, or K706 of the wide-type AAV2 capsid protein of SEQ ID NO:2.

3. The isolated nucleic acid molecule of claim 1 , wherein the modified AAV capsid protein comprises a non-lysine amino acid residue at a position that corresponds to K530, K547, or K569 of the wild-type AAV8 capsid protein of SEQ ID NO:8.

4. The isolated nucleic acid molecule of claim 1 , wherein the modified AAV capsid protein comprises a non-serine amino acid residue at a position that corresponds to S261, S264, S267, S276, S384, S458, S468, S492, S498, S578, S658, S662, S668, S707, or S721 of the wild-type AAV2 capsid protein of SEQ ID NO:2.

5. The isolated nucleic acid molecule of claim 1 , wherein the modified AAV capsid protein comprises a non-threonine amino acid residue at a position that corresponds to T251, T329, T330, T454, T455, T503, T550, T592, T581, T597, T491, T671, T659, T660, T701, T713, or T716 of the wild-type AAV2 capsid protein of SEQ ID NO:2.

6. The isolated nucleic acid molecule of claim 1 , wherein the modified AAV capsid protein comprises a non-lysine amino acid residue at a position that corresponds to K321, K490, K507, K527, K532, K549, K556, K649, K665, or K706 of the wild-type AAV2 capsid protein of SEQ ID NO:2.

7. The isolated nucleic acid molecule of claim 2 , wherein the non-lysine amino acid residue is glutamic acid (E) or arginine (R).

8. The isolated nucleic acid molecule of claim 7 , wherein the non-lysine amino acid residue is glutamic acid (E).

9. The isolated nucleic acid molecule of claim 3 , wherein the non-lysine amino acid residue is glutamic acid (E) or arginine (R).

10. The isolated nucleic acid molecule of claim 9 , wherein the non-lysine amino acid residue is glutamic acid (E).

11. The isolated nucleic acid molecule of claim 4 , wherein the non-serine amino acid residue is valine (V), aspartic acid (D), or histidine (H).

12. The isolated nucleic acid molecule of claim 11 , wherein the non-serine amino acid residue is valine (V).

13. The isolated nucleic acid molecule of claim 5 , wherein the non-threonine amino acid residue is valine (V).

14. The isolated nucleic acid molecule of claim 6 , wherein the non-lysine amino acid residue is glutamic acid (E) or arginine (R).

15. The isolated nucleic acid molecule of claim 14 , wherein the non-lysine amino acid residue is glutamic acid (E).

16. The isolated nucleic acid molecule of claim 1 , wherein the modified AAV capsid protein is a modified AAV1, AAV2, AAV3, AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, AAV10, AAV11 or AAV 12 capsid protein.

17. The isolated nucleic acid molecule of claim 1 , wherein the modified AAV capsid protein is a VP1 capsid protein.

18. The isolated nucleic acid molecule of claim 1 , wherein the modified AAV capsid protein is a VP2 capsid protein.

19. The isolated nucleic acid molecule of claim 1 , wherein the modified AAV capsid protein is a VP3 capsid protein.

Assignments (2)
CONFIRMATORY LICENSE Recorded Aug 16, 2017
From: UNIVERSITY OF FLORIDA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 043570/0126 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 19, 2017
From: SRIVASTAVA, ARUN; ASLANIDI, GEORGE VLADIMIROVICH; VAN VLIET, KIM M.; AGBANDJE-MCKENNA, MAVIS
To: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED
Reel/Frame 042748/0513 →
Continuity (4)
Division 14401442
Continuation 13840224 · Mar 15, 2013
Provisional Application 61647318 · May 15, 2012
Related Publication 20170275337A1 · Sep 28, 2017
Cited By (6)
US 12,358,954 US 12,472,268 US 12,544,437 US 12,570,699 US 12,649,006 US 12,686,874