Zhang Wei, Mukhopadhyay Suchetana, Pletnev Sergei V, Baker Timothy S, Kuhn Richard J, Rossmann Michael G
Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907-1392, USA.
J Virol. 2002 Nov;76(22):11645-58. doi: 10.1128/jvi.76.22.11645-11658.2002.
The structure of the lipid-enveloped Sindbis virus has been determined by fitting atomic resolution crystallographic structures of component proteins into an 11-A resolution cryoelectron microscopy map. The virus has T=4 quasisymmetry elements that are accurately maintained between the external glycoproteins, the transmembrane helical region, and the internal nucleocapsid core. The crystal structure of the E1 glycoprotein was fitted into the cryoelectron microscopy density, in part by using the known carbohydrate positions as restraints. A difference map showed that the E2 glycoprotein was shaped similarly to E1, suggesting a possible common evolutionary origin for these two glycoproteins. The structure shows that the E2 glycoprotein would have to move away from the center of the trimeric spike in order to expose enough viral membrane surface to permit fusion with the cellular membrane during the initial stages of host infection. The well-resolved E1-E2 transmembrane regions form alpha-helical coiled coils that were consistent with T=4 symmetry. The known structure of the capsid protein was fitted into the density corresponding to the nucleocapsid, revising the structure published earlier.
脂质包膜辛德毕斯病毒的结构已通过将组成蛋白的原子分辨率晶体结构拟合到11埃分辨率的冷冻电子显微镜图谱中得以确定。该病毒具有T = 4准对称元件,这些元件在外膜糖蛋白、跨膜螺旋区域和内部核衣壳核心之间精确保持。通过部分利用已知的碳水化合物位置作为约束条件,将E1糖蛋白的晶体结构拟合到冷冻电子显微镜密度图中。差异图显示E2糖蛋白的形状与E1相似,表明这两种糖蛋白可能有共同的进化起源。该结构表明,在宿主感染的初始阶段,E2糖蛋白必须从三聚体刺突的中心移开,以便暴露出足够的病毒膜表面,从而允许与细胞膜融合。解析良好的E1 - E2跨膜区域形成α - 螺旋卷曲螺旋,这与T = 4对称性一致。将衣壳蛋白的已知结构拟合到对应于核衣壳的密度图中,修正了先前发表的结构。