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马丘波病毒聚合酶与基质蛋白 Z 复合物的结构。

Structure of Machupo virus polymerase in complex with matrix protein Z.

机构信息

National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, 100101, Beijing, China.

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

出版信息

Nat Commun. 2021 Oct 25;12(1):6163. doi: 10.1038/s41467-021-26432-3.

Abstract

The Arenaviridae family includes several viruses that cause severe human hemorrhagic fevers with high mortality, with no effective countermeasures currently available. The arenavirus multi-domain L protein is involved in viral transcription and replication and represents a promising target for antiviral drugs. The arenavirus matrix protein Z is a small multi-functional protein that inhibits the activities of the L protein. Here we report the structure of Machupo virus L protein in complex with Z determined by cryo-electron microscopy. The Z protein acts as a staple and binds the L protein with 1:1 stoichiometry at the intersection between the PA-C-like region, RNA-dependent RNA polymerase and PB2-N-like region. Binding of the Z protein may lock the multiple domains of L into a fixed arrangement leading to loss of catalytic activity. These results further our understanding of the inhibitory mechanism of arenavirus replication machinery and provide a novel perspective to develop antiviral drugs.

摘要

沙粒病毒科包括几种可引起严重人类出血热、死亡率较高的病毒,目前尚无有效的应对措施。沙粒病毒多结构域 L 蛋白参与病毒转录和复制,是抗病毒药物的一个有前途的靶点。沙粒病毒基质蛋白 Z 是一种小的多功能蛋白,可抑制 L 蛋白的活性。本文通过冷冻电镜技术解析了 Machupo 病毒 L 蛋白与 Z 蛋白复合物的结构。Z 蛋白作为一个订书钉,以 1:1 的化学计量比与位于 PA-C 样区、RNA 依赖性 RNA 聚合酶和 PB2-N 样区交界处的 L 蛋白结合。Z 蛋白的结合可能将 L 蛋白的多个结构域锁定在固定的排列中,从而导致催化活性丧失。这些结果进一步了解了沙粒病毒复制机制的抑制机制,并为开发抗病毒药物提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6bc/8546121/402c4b1501ed/41467_2021_26432_Fig1_HTML.jpg

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