A cofactor for HIV-1 (human immunodeficiency virus-type 1) fusion and
entry was identified with the use of a novel functional complementary
DNA (cDNA) cloning strategy. This protein, designated ''fusin,'' is a
putative G protein-coupled receptor with seven transmembrane segments.
Recombinant fusin enabled CD4-expressing nonhuman cell types to suppo
rt HIV-1 Env-mediated cell fusion and HIV-1 infection. Antibodies to f
usin blocked cell fusion and infection with normal CD4-positive human
target cells. Fusin messenger RNA levels correlated with HIV-1 permiss
iveness in diverse human cell types. Fusin acted preferentially for T
cell line-tropic isolates, in comparison to its activity with macropha
ge-tropic HIV-1 isolates.