National Resource for Automated Molecular Microscopy, Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Science. 2012 Dec 21;338(6114):1631-4. doi: 10.1126/science.1227270. Epub 2012 Nov 22.
Influenza virus ribonucleoprotein complexes (RNPs) are central to the viral life cycle and in adaptation to new host species. RNPs are composed of the viral genome, viral polymerase, and many copies of the viral nucleoprotein. In vitro cell expression of all RNP protein components with four of the eight influenza virus gene segments enabled structural determination of native influenza virus RNPs by means of cryogenic electron microscopy (cryo-EM). The cryo-EM structure reveals the architecture and organization of the native RNP, defining the attributes of its largely helical structure and how polymerase interacts with nucleoprotein and the viral genome. Observations of branched-RNP structures in negative-stain electron microscopy and their putative identification as replication intermediates suggest a mechanism for viral replication by a second polymerase on the RNP template.
流感病毒核糖核蛋白复合物(RNPs)是病毒生命周期和适应新宿主物种的核心。RNPs 由病毒基因组、病毒聚合酶和许多病毒核蛋白组成。通过低温电子显微镜(cryo-EM),可以在体外细胞表达所有 RNP 蛋白成分和八个流感病毒基因片段中的四个,从而确定天然流感病毒 RNPs 的结构。cryo-EM 结构揭示了天然 RNP 的架构和组织,定义了其大部分螺旋结构的属性,以及聚合酶如何与核蛋白和病毒基因组相互作用。在负染电子显微镜中观察到分支 RNP 结构,并推测它们可能作为复制中间体,这表明了一种通过 RNP 模板上的第二种聚合酶进行病毒复制的机制。