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基孔肯雅病毒非结构蛋白1对病毒RNA加帽及质膜靶向作用的结构解析

Structural insights into viral RNA capping and plasma membrane targeting by Chikungunya virus nonstructural protein 1.

作者信息

Zhang Kuo, Law Yee-Song, Law Michelle Cheok Yien, Tan Yaw Bia, Wirawan Melissa, Luo Dahai

机构信息

Lee Kong Chian School of Medicine, Nanyang Technological University, EMB 03-07, 59 Nanyang Drive, Singapore 636921, Singapore; NTU Institute of Structural Biology, Nanyang Technological University, EMB 06-01, 59 Nanyang Drive, Singapore 636921, Singapore.

Lee Kong Chian School of Medicine, Nanyang Technological University, EMB 03-07, 59 Nanyang Drive, Singapore 636921, Singapore; NTU Institute of Structural Biology, Nanyang Technological University, EMB 06-01, 59 Nanyang Drive, Singapore 636921, Singapore; School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, Singapore 637551, Singapore.

出版信息

Cell Host Microbe. 2021 May 12;29(5):757-764.e3. doi: 10.1016/j.chom.2021.02.018. Epub 2021 Mar 16.

DOI:10.1016/j.chom.2021.02.018
PMID:33730549
Abstract

Chikungunya virus (CHIKV) causes a debilitating arthralgic inflammatory disease in humans. The multifunctional CHIKV protein, nsP1, facilitates virus RNA replication and transcription by anchoring the viral replication complex (RC) to plasma membrane vesicles and synthesizing the viral RNA 5' cap-0. Here, we report a cryo-EM structure of CHIKV nsP1 at 2.38 Å resolution. Twelve copies of nsP1 form a crown-shaped ring structure with a 7.5-nm-wide channel for mediating communication and exchange between the viral RC and the host cell. The catalytic site for viral RNA capping is located in a tunnel that is shaped by neighboring nsP1 molecules. Two membrane-association loops target nsP1 to the inner leaflet of the plasma membrane via palmitoylation and hydrophobic and electrostatic interactions. Our study provides the structural basis of viral RNA capping and RC assembly mediated by nsP1 and guides the development of antivirals targeting these essential steps of virus infection.

摘要

基孔肯雅病毒(CHIKV)会在人类中引发使人衰弱的关节炎性疾病。多功能的CHIKV蛋白nsP1通过将病毒复制复合体(RC)锚定到质膜囊泡并合成病毒RNA 5'帽-0来促进病毒RNA的复制和转录。在此,我们报告了分辨率为2.38 Å的CHIKV nsP1的冷冻电镜结构。十二个nsP1拷贝形成一个冠状环结构,带有一个7.5纳米宽的通道,用于介导病毒RC与宿主细胞之间的通讯和交换。病毒RNA加帽的催化位点位于由相邻nsP1分子形成的隧道中。两个膜结合环通过棕榈酰化以及疏水和静电相互作用将nsP1靶向质膜的内小叶。我们的研究提供了由nsP介导的病毒RNA加帽和RC组装的结构基础,并指导了针对病毒感染这些关键步骤的抗病毒药物的开发。

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