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多态下的贝纳病毒冷冻电镜结构揭示了病毒刺突的逐步脱落。

Cryo-EM structures of Banna virus in multiple states reveal stepwise detachment of viral spikes.

机构信息

CAS Key Laboratory of Special Pathogens, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, 430071, PR China.

University of Chinese Academy of Sciences, Beijing, 100049, PR China.

出版信息

Nat Commun. 2024 Mar 13;15(1):2284. doi: 10.1038/s41467-024-46624-x.

Abstract

Banna virus (BAV) is the prototype Seadornavirus, a class of reoviruses for which there has been little structural study. Here, we report atomic cryo-EM structures of three states of BAV virions-surrounded by 120 spikes (full virions), 60 spikes (partial virions), or no spikes (cores). BAV cores are double-layered particles similar to the cores of other non-turreted reoviruses, except for an additional protein component in the outer capsid shell, VP10. VP10 was identified to be a cementing protein that plays a pivotal role in the assembly of BAV virions by directly interacting with VP2 (inner capsid), VP8 (outer capsid), and VP4 (spike). Viral spikes (VP4/VP9 heterohexamers) are situated on top of VP10 molecules in full or partial virions. Asymmetrical electrostatic interactions between VP10 monomers and VP4 trimers are disrupted by high pH treatment, which is thus a simple way to produce BAV cores. Low pH treatment of BAV virions removes only the flexible receptor binding protein VP9 and triggers significant conformational changes in the membrane penetration protein VP4. BAV virions adopt distinct spatial organization of their surface proteins compared with other well-studied reoviruses, suggesting that BAV may have a unique mechanism of penetration of cellular endomembranes.

摘要

香蕉束顶病毒(BAV)是 Seadornavirus 属的原型病毒,该属的类病毒结构研究较少。在此,我们报告了三种状态的 BAV 病毒粒子的原子冷冻电镜结构:被 120 个刺突(完整病毒)、60 个刺突(部分病毒)或无刺突(核心)包围的病毒粒子;核心是类似于其他非塔式 Reoviridae 病毒的双层颗粒,除了外壳的外壳有额外的蛋白质组分 VP10。VP10 被鉴定为一种胶凝蛋白,通过与 VP2(内壳)、VP8(外壳)和 VP4(刺突)直接相互作用,在 BAV 病毒粒子的组装中发挥关键作用。病毒刺突(VP4/VP9 异六聚体)位于完整或部分病毒粒子的 VP10 分子顶部。在高 pH 值处理下,VP10 单体和 VP4 三聚体之间的不对称静电相互作用被破坏,因此这是产生 BAV 核心的一种简单方法。BAV 病毒粒子在低 pH 值处理下仅去除了灵活的受体结合蛋白 VP9,并触发膜渗透蛋白 VP4 发生显著的构象变化。与其他研究较好的 Reoviridae 病毒相比,BAV 病毒粒子的表面蛋白具有不同的空间组织,这表明 BAV 可能具有独特的穿透细胞内吞膜的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/10937716/5a768d3954ef/41467_2024_46624_Fig1_HTML.jpg

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