CPC C12N 15/8645 (2013.01) [A61K 48/0025 (2013.01); A61K 48/0058 (2013.01); C07K 7/00 (2013.01); C07K 7/04 (2013.01); C07K 14/005 (2013.01); C07K 14/775 (2013.01); C07K 16/00 (2013.01); C12N 15/79 (2013.01); C12N 15/85 (2013.01); C12N 15/86 (2013.01); C07K 14/00 (2013.01); C07K 14/075 (2013.01); C07K 19/00 (2013.01); C07K 2319/01 (2013.01); C07K 2319/30 (2013.01); C07K 2319/33 (2013.01); C12N 2310/141 (2013.01); C12N 2750/14145 (2013.01); C12N 2810/85 (2013.01)] | 17 Claims |
1. A method for delivering a transgene to a subject comprising:
administering a rAAV to a subject, wherein the rAAV comprises:
(i) a capsid protein having an N-terminally grafted heterologous targeting peptide, wherein:
(a) the capsid protein is a VP2 capsid protein that is not of an AAV2 serotype; and
(b) the targeting peptide is a CNS-targeting polypeptide consisting of the amino acid sequence set forth in SEQ ID NO: 5, that is inserted between the first and second amino acid residues of the VP2 capsid protein, and
(ii) a recombinant AAV vector comprising a transgene,
wherein the rAAV infects cells of a target tissue of the subject.
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