| Literature DB >> 10520998 |
D M Eckert1, V N Malashkevich, L H Hong, P A Carr, P S Kim.
Abstract
The HIV-1 gp41 protein promotes viral entry by mediating the fusion of viral and cellular membranes. A prominent pocket on the surface of a central trimeric coiled coil within gp41 was previously identified as a potential target for drugs that inhibit HIV-1 entry. We designed a peptide, IQN17, which properly presents this pocket. Utilizing IQN17 and mirror-image phage display, we identified cyclic, D-peptide inhibitors of HIV-1 infection that share a sequence motif. A 1.5 A cocrystal structure of IQN17 in complex with a D-peptide, and NMR studies, show that conserved residues of these inhibitors make intimate contact with the gp41 pocket. Our studies validate the pocket per se as a target for drug development. IQN17 and these D-peptide inhibitors are likely to be useful for development and identification of a new class of orally bioavailable anti-HIV drugs.Entities:
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Year: 1999 PMID: 10520998 DOI: 10.1016/s0092-8674(00)80066-5
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582