Passos Dario Oliveira, Li Min, Yang Renbin, Rebensburg Stephanie V, Ghirlando Rodolfo, Jeon Youngmin, Shkriabai Nikoloz, Kvaratskhelia Mamuka, Craigie Robert, Lyumkis Dmitry
Laboratory of Genetics and Helmsley Center for Genomic Medicine, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.
Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Science. 2017 Jan 6;355(6320):89-92. doi: 10.1126/science.aah5163.
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.
与所有逆转录病毒一样,HIV-1将其RNA基因组的病毒DNA(vDNA)拷贝不可逆地插入宿主靶DNA(tDNA)中。整合体是一种由病毒整合酶(IN)和线性vDNA末端组成的高阶核蛋白复合物,介导整合过程。高效整合到宿主染色质中会导致形成包含催化连接的vDNA和tDNA的链转移复合物(STC)。HIV-1整合体一直难以进行高分辨率结构研究。我们使用可溶性IN融合蛋白来促进结构研究,通过该研究我们展示了核心四聚体HIV-1 STC的高分辨率冷冻电子显微镜(cryo-EM)结构以及采用羧基末端结构域重排的高阶形式。不同的STC结构突出了HIV-1如何利用常见的逆转录病毒整合体核心结构来容纳不同的IN结构域模块进行组装。