用低温电子显微镜和层析成像技术测定包膜病毒粒子的结构

2区 医学 Q1 Medicine Advances in Virus Research Pub Date : 2019-01-01 Epub Date: 2019-08-20 DOI:10.1016/bs.aivir.2019.07.009
Robert Stass, Weng M Ng, Young Chan Kim, Juha T Huiskonen
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引用次数: 8

摘要

包膜病毒将其基因组包裹在脂质双分子层中,脂质双分子层由介导病毒进入的膜蛋白修饰。这些病毒的大小、形态和对称性各不相同。球形病毒通常是等距的,它们的包膜蛋白遵循二十面体对称。丝状和多形性病毒缺乏这种全局对称性,但它们的表面蛋白可能显示局部有序的组装。确定包膜病毒的结构,包括包膜蛋白及其在病毒表面的蛋白-蛋白相互作用,是至关重要的。这些结构可以揭示病毒粒子如何从被感染的宿主细胞出芽中组装和释放,子代病毒粒子如何通过膜融合感染新细胞,以及抗体如何结合表面表位阻止感染。在本章中,我们讨论了低温电子显微镜(cryo-EM)在阐明包膜病毒粒子结构中的应用。从数据收集和处理策略的详细概述开始,我们强调如何成功地利用低温电镜技术为包膜病毒的进入、组装和中和提供独特的见解。
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Structures of enveloped virions determined by cryogenic electron microscopy and tomography.

Enveloped viruses enclose their genomes inside a lipid bilayer which is decorated by membrane proteins that mediate virus entry. These viruses display a wide range of sizes, morphologies and symmetries. Spherical viruses are often isometric and their envelope proteins follow icosahedral symmetry. Filamentous and pleomorphic viruses lack such global symmetry but their surface proteins may display locally ordered assemblies. Determining the structures of enveloped viruses, including the envelope proteins and their protein-protein interactions on the viral surface, is of paramount importance. These structures can reveal how the virions are assembled and released by budding from the infected host cell, how the progeny virions infect new cells by membrane fusion, and how antibodies bind surface epitopes to block infection. In this chapter, we discuss the uses of cryogenic electron microscopy (cryo-EM) in elucidating structures of enveloped virions. Starting from a detailed outline of data collection and processing strategies, we highlight how cryo-EM has been successfully utilized to provide unique insights into enveloped virus entry, assembly, and neutralization.

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CiteScore
7.10
自引率
0.00%
发文量
7
审稿时长
>12 weeks
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