Inhibiting HIV-1 entry: Discovery of D-peptide inhibitors that target the gp41 coiled-coil pocket

被引:412
作者
Eckert, DM [1 ]
Malashkevich, VN [1 ]
Hong, LH [1 ]
Carr, PA [1 ]
Kim, PS [1 ]
机构
[1] MIT, Howard Hughes Med Inst, Whitehead Inst Biomed Res, Dept Biol,Cambridge Ctr 9, Cambridge, MA 02142 USA
关键词
D O I
10.1016/S0092-8674(00)80066-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. A1.5 Angstrom 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 ave likely to be useful for development and identification of a new class of orally bioavailable anti-HIV drugs.
引用
收藏
页码:103 / 115
页数:13
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