HIV-1 entry cofactor: Functional cDNA cloning of a seven-transmembrane, G protein-coupled receptor

Yu Feng, Christopher C. Broder, Paul E. Kennedy, Edward A. Berger*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3739 Scopus citations

Abstract

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 support HIV-1 Env-mediated cell fusion and HIV-1 infection. Antibodies to fusin blocked cell fusion and infection with normal CD4-positive human target cells. Fusin messenger RNA levels correlated with HIV-1 permissiveness in diverse human cell types. Fusin acted preferentially for T cell line-tropic isolates, in comparison to its activity with macrophage-tropic HIV-1 isolates.

Original languageEnglish
Pages (from-to)872-877
Number of pages6
JournalScience
Volume272
Issue number5263
DOIs
StatePublished - 1996

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