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丙型肝炎病毒核心蛋白羧基末端区的遗传分析。

Genetic analysis of the carboxy-terminal region of the hepatitis C virus core protein.

机构信息

Laboratory of Virology and Infectious Disease, Center for the Study of Hepatitis C, The Rockefeller University, 1230 York Ave., New York, NY 10065, USA.

出版信息

J Virol. 2010 Feb;84(4):1666-73. doi: 10.1128/JVI.02043-09. Epub 2009 Dec 9.

DOI:10.1128/JVI.02043-09
PMID:20007277
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2812405/
Abstract

Hepatitis C virus (HCV) is a liver-tropic pathogen with severe health consequences for infected individuals. Chronic HCV infection can progress to cirrhosis and hepatocellular carcinoma and is a leading indicator for liver transplantation. The HCV core protein is an essential component of the infectious virus particle, but many aspects of its role remain undefined. The C-terminal region of the core protein acts as a signal sequence for the E1 glycoprotein and undergoes dual processing events during infectious virus assembly. The exact C terminus of the mature, virion-associated core protein is not known. Here, we performed genetic analyses to map the essential determinants of the HCV core C-terminal region, as well as to define the minimal length of the protein that can function for infectious virus production in trans.

摘要

丙型肝炎病毒(HCV)是一种嗜肝病原体,对感染个体的健康有严重影响。慢性 HCV 感染可进展为肝硬化和肝细胞癌,是肝移植的主要指征。HCV 核心蛋白是感染性病毒颗粒的重要组成部分,但它的许多作用仍未得到明确。核心蛋白的 C 末端区域充当 E1 糖蛋白的信号序列,并在感染性病毒组装过程中经历双重加工事件。成熟的、与病毒相关的核心蛋白的确切 C 末端尚不清楚。在这里,我们进行了遗传分析,以确定 HCV 核心 C 末端区域的必需决定因素,并确定可用于转染产生感染性病毒的蛋白的最小长度。

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Characterization of determinants important for hepatitis C virus p7 function in morphogenesis by using trans-complementation.利用反式互补对丙型肝炎病毒p7在形态发生中功能的重要决定因素进行表征。
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Characterization of hepatitis C virus core protein multimerization and membrane envelopment: revelation of a cascade of core-membrane interactions.丙型肝炎病毒核心蛋白多聚化及膜包裹的特征:核心-膜相互作用级联反应的揭示
J Virol. 2009 Oct;83(19):9923-39. doi: 10.1128/JVI.00066-09. Epub 2009 Jul 15.
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Hepatitis C virus NS2 protein contributes to virus particle assembly via opposing epistatic interactions with the E1-E2 glycoprotein and NS3-NS4A enzyme complexes.丙型肝炎病毒NS2蛋白通过与E1-E2糖蛋白和NS3-NS4A酶复合物的上位性相互作用来促进病毒粒子组装。
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