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病毒粒子的组装和释放。

Virion assembly and release.

机构信息

Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT 06536, USA.

出版信息

Curr Top Microbiol Immunol. 2013;369:199-218. doi: 10.1007/978-3-642-27340-7_8.

DOI:10.1007/978-3-642-27340-7_8
PMID:23463202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3925669/
Abstract

Hepatitis C Virus (HCV) particles exhibit several unusual properties that are not found in other enveloped RNA viruses, most notably their low buoyant density and interaction with serum lipoproteins. With the advent of systems to grow HCV in cell culture, the molecular basis of HCV particle assembly and release can now be addressed. The process of virus assembly involves protein-protein interactions between viral structural and nonstructural proteins and the coordinated action of host factors. This chapter reviews our current understanding of these interactions and factors.

摘要

丙型肝炎病毒(HCV)颗粒表现出几种在其他包膜 RNA 病毒中未发现的异常特性,最显著的是其较低的浮力密度和与血清脂蛋白的相互作用。随着在细胞培养中培养 HCV 的系统的出现,现在可以解决 HCV 颗粒组装和释放的分子基础。病毒组装的过程涉及病毒结构蛋白和非结构蛋白之间的蛋白-蛋白相互作用以及宿主因子的协调作用。本章回顾了我们对这些相互作用和因素的现有认识。

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本文引用的文献

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Identification and targeting of an interaction between a tyrosine motif within hepatitis C virus core protein and AP2M1 essential for viral assembly.鉴定和靶向丙型肝炎病毒核心蛋白内的酪氨酸基序与 AP2M1 之间的相互作用,该基序对于病毒组装是必需的。
PLoS Pathog. 2012;8(8):e1002845. doi: 10.1371/journal.ppat.1002845. Epub 2012 Aug 16.
2
MAP-kinase regulated cytosolic phospholipase A2 activity is essential for production of infectious hepatitis C virus particles.MAP-kinase 调节的细胞质磷脂酶 A2 活性对于感染性丙型肝炎病毒颗粒的产生是必需的。
PLoS Pathog. 2012;8(7):e1002829. doi: 10.1371/journal.ppat.1002829. Epub 2012 Jul 26.
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探索宿主细胞膜中阴离子脂质对病毒融合的影响。
Biochem Soc Trans. 2024 Dec 19;52(6):2593-2602. doi: 10.1042/BST20240833.
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Poly(rC)-Binding Protein 2 Does Not Directly Participate in HCV Translation or Replication, but Rather Modulates Genome Packaging.聚(C)结合蛋白 2 不直接参与 HCV 翻译或复制,而是调节基因组包装。
Viruses. 2024 Jul 30;16(8):1220. doi: 10.3390/v16081220.
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After the Storm: Persistent Molecular Alterations Following HCV Cure.《风暴过后:HCV 治愈后的持续分子改变》
Int J Mol Sci. 2024 Jun 27;25(13):7073. doi: 10.3390/ijms25137073.
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Involvement of ribosomal protein L17 and Y-box binding protein 1 in the assembly of hepatitis C virus potentially via their interaction with the 3' untranslated region of the viral genome.核糖体蛋白 L17 和 Y 盒结合蛋白 1 参与丙型肝炎病毒的组装,可能是通过与病毒基因组的 3'非翻译区相互作用。
J Virol. 2024 Jul 23;98(7):e0052224. doi: 10.1128/jvi.00522-24. Epub 2024 Jun 20.
7
Lipid Profile and Cardiovascular Risk Modification after Hepatitis C Virus Eradication.丙型肝炎病毒根除后的血脂谱与心血管风险改善
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A Hepatitis C virus genotype 1b post-transplant isolate with high replication efficiency in cell culture and its adaptation to infectious virus production in vitro and in vivo.一株丙型肝炎病毒 1b 型移植后分离株,在细胞培养中具有高复制效率,并且能够适应体外和体内感染性病毒的产生。
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Analysis of functional differences between hepatitis C virus NS5A of genotypes 1-7 in infectious cell culture systems.分析在感染细胞培养系统中基因型 1-7 的丙型肝炎病毒 NS5A 之间的功能差异。
PLoS Pathog. 2012;8(5):e1002696. doi: 10.1371/journal.ppat.1002696. Epub 2012 May 24.
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Regulation of hepatitis C virus secretion by the Hrs-dependent exosomal pathway.Hrs 依赖的外泌体途径对丙型肝炎病毒分泌的调控。
Virology. 2012 Jan 20;422(2):377-85. doi: 10.1016/j.virol.2011.11.009. Epub 2011 Dec 3.
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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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A genetic interaction between the core and NS3 proteins of hepatitis C virus is essential for production of infectious virus.丙型肝炎病毒核心蛋白和 NS3 蛋白之间的遗传相互作用对于产生感染性病毒是必需的。
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