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AssigneeThe Trustees of the University of Pennsylvania
InventorsJames M. Wilson, Christie L. Bell, Luc H. Vandenberghe
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A method of altering the targeting and/or cellular uptake efficiency of an adeno-associated virus (AAV) viral vector having a capsid containing an AAV9 cell surface binding domain is described. The method involves modifying a clade F cell surface receptor which comprises a glycan having a terminal sialic acid residue and a penultimate β-galactose residue. The modification may involve retargeting the vector by temporarily functionally ablate AAV9 binding in a subset of cells, thereby redirecting the vector to another subset of cells. Alternatively, the modification may involve increasing cellular update efficiency by treating the cells with a neuraminidase to expose cell surface β-galactose. Also provided are compositions containing the AAV9 vector and a neuraminidase. Also provided is a method for purifying AAV9 using β-galactose linked to solid support. Also provided are mutant vectors which have been modified to alter their targeting specificity, including mutant AAV9 in which the galactose binding domain is mutated and AAV in which an AAV9 galactose binding domain is engineered.
A recombinant adeno-associated virus (AAV) 9 (AAV9) viral particle modified to substantially decrease or ablate the native ability of wild-type (wt) AAV9 to transduce conducting airway, said viral particle having an AAV9 capsid protein in which a native AAV9 amino acid selected from the group consisting of position 271, 446, or 470 based on the positions of SEQ ID NO:
A recombinant clade F adeno-associated virus (AAV) viral particle modified to substantially decrease or ablate the native ability of wild-type (wt) AAV to transduce conducting airway, said viral particle having an AAV capsid protein in which a native AAV amino acid selected from the group consisting of position 271, 446, or 470 based on the positions of SEQ ID NO:
A method of generating a recombinant AAV viral particle, wherein the recombinant viral particle comprises an AAV capsid protein with an engineered AAV9 cell binding domain, said cell binding domain comprising amino acids Y446, N470, A472, V473, D271, N272 and W503 which forms a galactose binding domain, wherein the amino acid numbering is based on the positions of SEQ ID NO:
A kit comprising a solid support having β-galactose containing molecule linked thereto.
Dependencies are inferred from the claim text.