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2
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Structural and functional studies of nonstructural protein 2 of the hepatitis C virus reveal its key role as organizer of virion assembly.丙型肝炎病毒非结构蛋白 2 的结构和功能研究揭示了其作为病毒组装组织者的关键作用。
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磷脂酰丝氨酸特异性磷脂酶 A1 是丙型肝炎病毒组装的关键桥梁。

Phosphatidylserine-Specific Phospholipase A1 is the Critical Bridge for Hepatitis C Virus Assembly.

机构信息

Department of Gastroenterology, Guangzhou Women and Children's Medical Center, Guangzhou, 510623, China.

State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, 430071, China.

出版信息

Virol Sin. 2019 Oct;34(5):521-537. doi: 10.1007/s12250-019-00123-2. Epub 2019 Jun 3.

DOI:10.1007/s12250-019-00123-2
PMID:31161554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6814691/
Abstract

The phosphatidylserine-specific phospholipase A1 (PLA1A) is an essential host factor in hepatitis C virus (HCV) assembly. In this study, we mapped the E2, NS2 and NS5A involved in PLA1A interaction to their lumenal domains and membranous parts, through which they form oligomeric protein complexes to participate in HCV assembly. Multiple regions of PLA1A were involved in their interaction and complex formation. Furthermore, the results represented structures with PLA1A and E2 in closer proximity than NS2 and NS5A, and strongly suggest PLA1A-E2's physical interaction in cells. Meanwhile, we mapped the NS5A sequence which participated in PLA1A interaction with the C-terminus of domain 1. Interestingly, these amino acids in the sequence are also essential for viral RNA replication. Further experiments revealed that these four proteins interact with each other. Moreover, PLA1A expression levels were elevated in livers from HCV-infected patients. In conclusion, we exposed the structural determinants of PLA1A, E2, NS2 and NS5A proteins which were important for HCV assembly and provided a detailed characterization of PLA1A in HCV assembly.

摘要

磷脂酰丝氨酸特异性磷脂酶 A1(PLA1A)是丙型肝炎病毒(HCV)组装所必需的宿主因子。在这项研究中,我们通过腔域和膜部分将参与 PLA1A 相互作用的 E2、NS2 和 NS5A 映射到它们的位置,通过这些位置,它们形成寡聚蛋白复合物以参与 HCV 组装。PLA1A 的多个区域参与了它们的相互作用和复合物形成。此外,结果代表了与 PLA1A 和 E2 更接近的结构,而与 NS2 和 NS5A 则不那么接近,并且强烈表明 PLA1A-E2 在细胞中存在物理相互作用。同时,我们将参与 PLA1A 相互作用的 NS5A 序列映射到结构域 1 的 C 末端。有趣的是,该序列中的这些氨基酸对于病毒 RNA 复制也是必需的。进一步的实验表明,这四种蛋白质相互作用。此外,在 HCV 感染患者的肝脏中 PLA1A 的表达水平升高。总之,我们揭示了 PLA1A、E2、NS2 和 NS5A 蛋白对于 HCV 组装很重要的结构决定因素,并详细描述了 PLA1A 在 HCV 组装中的作用。