| Literature DB >> 28059769 |
Dario Oliveira Passos1, Min Li2, Renbin Yang2, Stephanie V Rebensburg3, Rodolfo Ghirlando2, Youngmin Jeon1, Nikoloz Shkriabai3, Mamuka Kvaratskhelia3, Robert Craigie2, Dmitry Lyumkis4.
Abstract
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.Entities:
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Year: 2017 PMID: 28059769 PMCID: PMC5508583 DOI: 10.1126/science.aah5163
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728