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丙型肝炎病毒感染性颗粒的形态发生

Morphogenesis of infectious hepatitis C virus particles.

作者信息

Suzuki Tetsuro

机构信息

Department of Infectious Diseases, Hamamatsu University School of Medicine Hamamatsu, Japan.

出版信息

Front Microbiol. 2012 Feb 7;3:38. doi: 10.3389/fmicb.2012.00038. eCollection 2012.

DOI:10.3389/fmicb.2012.00038
PMID:22347224
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3273859/
Abstract

More than 170 million individuals are currently infected with hepatitis C virus (HCV) worldwide and are at continuous risk of developing chronic liver disease. Since a cell culture system enabling relatively efficient propagation of HCV has become available, an increasing number of viral and host factors involved in HCV particle formation have been identified. Association of the viral Core, which forms the capsid with lipid droplets appears to be prerequisite for early HCV morphogenesis. Maturation and release of HCV particles is tightly linked to very-low-density lipoprotein biogenesis. Although expression of Core as well as E1 and E2 envelope proteins produces virus-like particles in heterologous expression systems, there is increasing evidence that non-structural viral proteins and p7 are also required for the production of infectious particles, suggesting that HCV genome replication and virion assembly are closely linked. Advances in our understanding of the various molecular mechanisms by which infectious HCV particles are formed are summarized.

摘要

目前全球有超过1.7亿人感染丙型肝炎病毒(HCV),且持续面临发展为慢性肝病的风险。自从一种能够使HCV相对高效繁殖的细胞培养系统问世以来,越来越多参与HCV颗粒形成的病毒和宿主因子被识别出来。病毒核心蛋白(Core)与脂滴形成衣壳,其关联似乎是HCV早期形态发生的先决条件。HCV颗粒的成熟和释放与极低密度脂蛋白的生物合成紧密相关。尽管在异源表达系统中,Core以及E1和E2包膜蛋白的表达可产生病毒样颗粒,但越来越多的证据表明,非结构病毒蛋白和p7对于产生感染性颗粒也是必需的,这表明HCV基因组复制和病毒体组装密切相关。本文总结了我们对感染性HCV颗粒形成的各种分子机制的理解进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6cf/3273859/169aa47e3eb4/fmicb-03-00038-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6cf/3273859/5edac23779ba/fmicb-03-00038-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6cf/3273859/169aa47e3eb4/fmicb-03-00038-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6cf/3273859/5edac23779ba/fmicb-03-00038-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6cf/3273859/169aa47e3eb4/fmicb-03-00038-g002.jpg

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本文引用的文献

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Trafficking of hepatitis C virus core protein during virus particle assembly.丙型肝炎病毒核心蛋白在病毒粒子组装过程中的转运。
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Hepatitis C Virus Particle Assembly Involves Phosphorylation of NS5A by the c-Abl Tyrosine Kinase.丙型肝炎病毒颗粒组装涉及c-Abl酪氨酸激酶对NS5A的磷酸化作用。
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Apolipoprotein E, but Not Apolipoprotein B, Is Essential for Efficient Cell-to-Cell Transmission of Hepatitis C Virus.载脂蛋白E而非载脂蛋白B是丙型肝炎病毒高效细胞间传播所必需的。
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NS2 protein of hepatitis C virus interacts with structural and non-structural proteins towards virus assembly.丙型肝炎病毒 NS2 蛋白与结构蛋白和非结构蛋白相互作用,促进病毒组装。
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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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Hepatitis C virus NS2 coordinates virus particle assembly through physical interactions with the E1-E2 glycoprotein and NS3-NS4A enzyme complexes.丙型肝炎病毒 NS2 通过与 E1-E2 糖蛋白和 NS3-NS4A 酶复合物的物理相互作用来协调病毒粒子的组装。
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Assembly of infectious hepatitis C virus particles.丙型肝炎病毒颗粒的组装。
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Hepatitis C virus NS2 protein serves as a scaffold for virus assembly by interacting with both structural and nonstructural proteins.丙型肝炎病毒 NS2 蛋白通过与结构蛋白和非结构蛋白相互作用,充当病毒组装的支架。
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Identification of basic amino acids at the N-terminal end of the core protein that are crucial for hepatitis C virus infectivity.鉴定核心蛋白 N 末端对于丙型肝炎病毒感染至关重要的碱性氨基酸。
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