Thogoto 病毒核蛋白的结构特征为了解病毒 RNA 封装和 RNP 组装提供了线索

IF 4.4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Alexej Dick, Vasilii Mikirtumov, Jonas Fuchs, Ferdinand Krupp, Daniel Olal, Elias Bendl, Thiemo Sprink, Christoph Diebolder, Mikhail Kudryashev, Georg Kochs, Yvette Roske, Oliver Daumke
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引用次数: 0

摘要

正粘病毒(如流感病毒和致病病毒)是重要的人类和动物病原体。它们的分段病毒 RNA 基因组被病毒核蛋白(NPs)包裹成螺旋状核糖核蛋白复合物(RNPs)。目前已报道了几种流感病毒的核蛋白结构。然而,关于正粘病毒 RNPs 是如何组装的,目前仍存在相互矛盾的模型。在这里,我们描述了Thogoto病毒(THOV)NP的晶体结构,发现它与流感病毒NP的结构有惊人的相似之处,包括双叶结构域、带正电荷的RNA结合裂隙以及对三聚体化和病毒转录很重要的尾环。THOV RNPs的低分辨率低温电子断层扫描重建阐明了左手双螺旋组装。我们的研究为 THOV 的 RNP 组装提供了一个模型,从而为鼻疽病毒和流感病毒提供了保守的 NP 组装和 RNA 封装模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Structural characterization of Thogoto Virus nucleoprotein provides insights into viral RNA encapsidation and RNP assembly

Structural characterization of Thogoto Virus nucleoprotein provides insights into viral RNA encapsidation and RNP assembly

Orthomyxoviruses, such as influenza and thogotoviruses, are important human and animal pathogens. Their segmented viral RNA genomes are wrapped by viral nucleoproteins (NPs) into helical ribonucleoprotein complexes (RNPs). NP structures of several influenza viruses have been reported. However, there are still contradictory models of how orthomyxovirus RNPs are assembled. Here, we characterize the crystal structure of Thogoto virus (THOV) NP and found striking similarities to structures of influenza viral NPs, including a two-lobed domain architecture, a positively charged RNA-binding cleft, and a tail loop important for trimerization and viral transcription. A low-resolution cryo-electron tomography reconstruction of THOV RNPs elucidates a left-handed double helical assembly. By providing a model for RNP assembly of THOV, our study suggests conserved NP assembly and RNA encapsidation modes for thogoto- and influenza viruses.

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来源期刊
Structure
Structure 生物-生化与分子生物学
CiteScore
8.90
自引率
1.80%
发文量
155
审稿时长
3-8 weeks
期刊介绍: Structure aims to publish papers of exceptional interest in the field of structural biology. The journal strives to be essential reading for structural biologists, as well as biologists and biochemists that are interested in macromolecular structure and function. Structure strongly encourages the submission of manuscripts that present structural and molecular insights into biological function and mechanism. Other reports that address fundamental questions in structural biology, such as structure-based examinations of protein evolution, folding, and/or design, will also be considered. We will consider the application of any method, experimental or computational, at high or low resolution, to conduct structural investigations, as long as the method is appropriate for the biological, functional, and mechanistic question(s) being addressed. Likewise, reports describing single-molecule analysis of biological mechanisms are welcome. In general, the editors encourage submission of experimental structural studies that are enriched by an analysis of structure-activity relationships and will not consider studies that solely report structural information unless the structure or analysis is of exceptional and broad interest. Studies reporting only homology models, de novo models, or molecular dynamics simulations are also discouraged unless the models are informed by or validated by novel experimental data; rationalization of a large body of existing experimental evidence and making testable predictions based on a model or simulation is often not considered sufficient.
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