We have designed and constructed retrovirus particles displaying the I
gG-binding domain of protein A. We fused the gene for the synthetic an
tibody-binding portion of protein A with the envelope gene of ecotropi
c Moloney murine leukemia virus. The fusion gene was coexpressed in ec
otropic retroviral packaging cells, and retrovirus particles with IgG-
binding activities mere recovered. In principle, the protein A-envelop
e chimeric retrovirus complexed with specific monoclonal antibody coul
d be used for cell-targeted gene delivery. (C) 1997 Academic Press.