Structural Biology of HIV Integrase Strand Transfer Inhibitors

被引:35
作者
Jozwik, Ilona K. [1 ]
Passos, Dario O. [1 ]
Lyumkis, Dmitry [1 ,2 ]
机构
[1] Salk Inst Biol Studies, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA
[2] Scripps Res Inst, 10550 North Torrey Pines Rd, La Jolla, CA 92037 USA
关键词
IMMUNODEFICIENCY-VIRUS-INFECTION; ANTIVIRAL ACTIVITY; CRYO-EM; PREINTEGRATION COMPLEXES; RESISTANCE MUTATIONS; DRUG-RESISTANCE; LIGAND-BINDING; RALTEGRAVIR; 2ND-GENERATION; PROTEIN;
D O I
10.1016/j.tips.2020.06.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Integrase (IN) strand transfer inhibitors (INSTIs) are recent compounds in the antiretroviral arsenal used against HIV. INSTIs work by blocking retroviral inte-gration; an essential step in the viral lifecycle that is catalyzed by the virally encoded IN protein within a nucleoprotein assembly called an intasome. Recent structures of lentiviral intasomes from simian immunodeficiency virus (SIV) and HIV have clarified the INSTI binding modes within the intasome active sites and helped elucidate an important mechanism of viral resistance. The structures pro-vide an accurate depiction of interactions of intasomes and INSTIs to be lever-aged for structure-based drug design. Here, we review these recent structural findings and contrast with earlier studies on prototype foamy virus intasomes. We also present and discuss examples of the latest chemical compounds that show promising inhibitory potential as INSTI candidates.
引用
收藏
页码:611 / 626
页数:16
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