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II类融合病毒的动态包膜。电子冷冻显微镜揭示的Semliki森林病毒的融合前阶段。

The dynamic envelope of a fusion class II virus. Prefusion stages of semliki forest virus revealed by electron cryomicroscopy.

作者信息

Wu Shang-Rung, Haag Lars, Hammar Lena, Wu Bomu, Garoff Henrik, Xing Li, Murata Kazuyoshi, Cheng R Holland

机构信息

Department of Biosciences and Nutrition, Karolinska Institutet, S-141 57 Huddinge, Sweden.

出版信息

J Biol Chem. 2007 Mar 2;282(9):6752-62. doi: 10.1074/jbc.M609125200. Epub 2006 Dec 27.

Abstract

Semliki Forest virus is among the prototypes for Class II virus fusion and targets the endosomal membrane. Fusion protein E1 and its envelope companion E2 are both anchored in the viral membrane and form an external shell with protruding spikes. In acid environments, mimicking the early endosomal milieu, surface epitopes in the virus rearrange along with exposure of the fusion loop. To visualize this transformation into a fusogenic stage, we determined the structure of the virus at gradually lower pH values. The results show that while the fusion loop is available for external interaction and the shell and stalk domains of the spike begin to deteriorate, the E1 and E2 remain in close contact in the spike head. This unexpected observation points to E1 and E2 cooperation beyond the fusion loop exposure stage and implies a more prominent role for E2 in guiding membrane close encounter than has been earlier anticipated.

摘要

塞姆利基森林病毒是II类病毒融合的原型之一,其靶向内体膜。融合蛋白E1及其包膜伴侣E2均锚定在病毒膜中,并形成带有突出刺突的外壳。在模拟早期内体环境的酸性环境中,病毒表面表位会随着融合环的暴露而重新排列。为了可视化这种向融合阶段的转变,我们测定了在逐渐降低的pH值下病毒的结构。结果表明,虽然融合环可用于外部相互作用,且刺突的外壳和茎域开始降解,但E1和E2在刺突头部仍保持紧密接触。这一意外发现表明E1和E2在融合环暴露阶段之后仍存在合作,并且意味着E2在引导膜紧密接触方面的作用比之前预期的更为突出。

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