4.8 Article

Cryo-EM structures and atomic model of the HIV-1 strand transfer complex intasome

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SCIENCE
卷 355, 期 6320, 页码 89-92

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AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aah5163

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资金

  1. NIH [P50 GM103368, R01 AI062520, P41 GM103331]
  2. Leona M. and Harry B. Helmsley Charitable Trust [2012-PG-MED002]
  3. National Institute of Diabetes and Digestive Diseases of the NIH
  4. Intramural AIDS Targeted Antiviral Program of the Office of the Director of the NIH

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Like all retroviruses, HIV-1 irreversibly inserts a viral DNA (vDNA) copy of its RNA genome into host target DNA (tDNA). The intasome, a higher-order nucleoprotein complex composed of viral integrase (IN) and the ends of linear vDNA, mediates integration. Productive integration into host chromatin results in the formation of the strand transfer complex (STC) containing catalytically joined vDNA and tDNA. HIV-1 intasomes have been refractory to high-resolution structural studies. We used a soluble IN fusion protein to facilitate structural studies, through which we present a high-resolution cryo-electron microscopy (cryo-EM) structure of the core tetrameric HIV-1 STC and a higher-order form that adopts carboxyl-terminal domain rearrangements. The distinct STC structures highlight how HIV-1 can use the common retroviral intasome core architecture to accommodate different IN domain modules for assembly.

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