Dryden K A, Wang G, Yeager M, Nibert M L, Coombs K M, Furlong D B, Fields B N, Baker T S
Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907.
J Cell Biol. 1993 Sep;122(5):1023-41. doi: 10.1083/jcb.122.5.1023.
Three structural forms of type 1 Lang reovirus (virions, intermediate subviral particles [ISVPs], and cores) have been examined by cryoelectron microscopy (cryoEM) and image reconstruction at 27 to 32-A resolution. Analysis of the three-dimensional maps and known biochemical composition allows determination of capsid protein location, globular shape, stoichiometry, quaternary organization, and interactions with adjacent capsid proteins. Comparisons of the virion, ISVP and core structures and examination of difference maps reveal dramatic changes in supra-molecular structure and protein conformation that are related to the early steps of reovirus infection. The intact virion (approximately 850-A diam) is designed for environmental stability in which the dsRNA genome is protected not only by tight sigma 3-mu 1, lambda 2-sigma 3, and lambda 2-mu 1 interactions in the outer capsid but also by a densely packed core shell formed primarily by lambda 1 and sigma 2. The segmented genome appears to be packed in a liquid crystalline fashion at radii < 240 A. Depending on viral growth conditions, virions undergo cleavage by enteric or endosomal/lysosomal proteases, to generate the activated ISVP (approximately 800-A diam). This transition involves the release of an outer capsid layer spanning radii from 360 to 427 A that is formed by 60 tetrameric and 60 hexameric clusters of ellipsoidal subunits of sigma 3. The vertex-associated cell attachment protein, sigma 1, also undergoes a striking change from a poorly visualized, more compact form, to an extended, flexible fiber. This conformational change may maximize interactions of sigma 1 with cell surface receptors. Transcription of viral mRNAs is mediated by the core particle (approximately 600-A diam), generated from the ISVP after penetration and uncoating. The transition from ISVP to core involves release of the 12 sigma 1 fibers and the remaining outer capsid layer formed by 200 trimers of rod-shaped mu 1 subunits that span radii from 306 to 395 A. In the virion and ISVP, flower-shaped pentamers of the lambda 2 protein are centered at the vertices. In the ISVP-to-core transition, domains of the lambda 2 subunits rotate and swing upward and outward to form a turret-like structure extending from radii 305 to 400 A, with a diameter of 184 A, and a central channel 84 A wide. This novel conformational change allows the potential diffusion of substrates for transcription and exit of newly synthesized mRNA segments.(ABSTRACT TRUNCATED AT 400 WORDS)
通过冷冻电子显微镜(cryoEM)和27至32埃分辨率的图像重建技术,对1型呼肠孤病毒的三种结构形式(病毒粒子、中间亚病毒颗粒[ISVPs]和核心)进行了研究。对三维图谱和已知生化组成的分析,有助于确定衣壳蛋白的位置、球状形状、化学计量、四级结构以及与相邻衣壳蛋白的相互作用。对病毒粒子、ISVP和核心结构的比较以及差异图谱的检查,揭示了与呼肠孤病毒感染早期步骤相关的超分子结构和蛋白质构象的显著变化。完整的病毒粒子(直径约850埃)设计用于环境稳定性,其中双链RNA基因组不仅受到外衣壳中紧密的σ3-μ1、λ2-σ3和λ2-μ1相互作用的保护,还受到主要由λ1和σ2形成的紧密堆积的核心壳的保护。分段基因组似乎以液晶形式堆积在半径小于240埃的区域。根据病毒生长条件,病毒粒子会被肠道或内体/溶酶体蛋白酶切割,产生活化的ISVP(直径约800埃)。这种转变涉及释放一个半径从360到427埃的外衣壳层,该外衣壳层由60个σ3椭球形亚基的四聚体簇和60个六聚体簇组成。与顶点相关的细胞附着蛋白σ1也经历了显著变化,从难以看清的、更紧凑的形式转变为伸展的、灵活的纤维。这种构象变化可能会使σ1与细胞表面受体的相互作用最大化。病毒mRNA的转录由核心颗粒(直径约600埃)介导,核心颗粒是在穿透和脱壳后由ISVP产生的。从ISVP到核心的转变涉及释放12根σ1纤维和由200个杆状μ1亚基三聚体形成的剩余外衣壳层,这些亚基跨度为半径从306到395埃。在病毒粒子和ISVP中,λ2蛋白的花状五聚体位于顶点中心。在从ISVP到核心的转变过程中,λ2亚基的结构域旋转并向上和向外摆动,形成一个从半径305到400埃延伸的炮塔状结构,直径为184埃,中央通道宽84埃。这种新的构象变化使得转录底物有可能扩散,并使新合成的mRNA片段得以输出。(摘要截断于400字)