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Structural Biology of HIV Integrase Strand Transfer Inhibitors

期刊

TRENDS IN PHARMACOLOGICAL SCIENCES
卷 41, 期 9, 页码 611-626

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CELL PRESS
DOI: 10.1016/j.tips.2020.06.003

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资金

  1. NIH [R01 AI136680, R01 AI146017, U54 AI150472, P41 GM103311]
  2. Margaret T. Morris Foundation

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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.

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