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丙型肝炎病毒蛋白的结构与功能:十五年后

Structure and functions of hepatitis C virus proteins: 15 years after.

作者信息

Krekulová L, Rehák V, Riley L W

机构信息

Hepatology, Nusle Clinic, Remedis--Nusle Clinic, Prague, Czechia

出版信息

Folia Microbiol (Praha). 2006;51(6):665-80. doi: 10.1007/BF02931636.

Abstract

Since its discovery in 1988, the hepatitis C virus (HCV) has become a hot topic of research by many groups around the world. This globally spread infectious agent is responsible for a large proportion of chronic viral hepatitides. The clue to halting the hepatitis C pandemic may be the detailed understanding of the virus structure, its replication mechanism, and the exact functions of the various proteins. Such understanding could enable the development of new antivirals targeted against hepatitis C virus and possibly an effective vaccine. This review recaps the current knowledge about the HCV genome 15 years after its discovery. The structure and function of particular viral structural (core, E1, E2) and nonstructural (NS2, NS3, NS4, NS5) proteins and noncoding regions known to date are described. With respect to frequent conflicting reports from different research groups, results reproducibly demonstrated by independent investigators are emphasized. Owing to many obstacles and limitations inherent in doing research on this noteworthy virus, the current knowledge is incomplete and the answers to many important questions are to be expected in the future.

摘要

自1988年被发现以来,丙型肝炎病毒(HCV)已成为全球众多研究团队的热门研究课题。这种在全球传播的传染源导致了很大一部分慢性病毒性肝炎。阻止丙型肝炎大流行的关键可能在于详细了解病毒结构、其复制机制以及各种蛋白质的确切功能。这样的了解能够推动针对丙型肝炎病毒的新型抗病毒药物的研发,并有可能研制出有效的疫苗。这篇综述在丙型肝炎病毒发现15年后总结了当前关于其基因组的知识。描述了迄今已知的特定病毒结构蛋白(核心蛋白、E1蛋白、E2蛋白)和非结构蛋白(NS2蛋白、NS3蛋白、NS4蛋白、NS5蛋白)以及非编码区的结构和功能。鉴于不同研究团队频繁出现相互矛盾的报告,重点强调了独立研究者可重复验证的结果。由于对这种重要病毒进行研究存在许多固有的障碍和局限性,目前的知识并不完整,许多重要问题的答案有望在未来得到解答。

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