Dubuisson Jean
Hepatitis C Laboratory, CNRS-UMR8161, Institut de Biologie de Lille I & II, Université de Lille, 1 rue Calmette, BP447, 59021 Lille Cedex, France.
World J Gastroenterol. 2007 May 7;13(17):2406-15. doi: 10.3748/wjg.v13.i17.2406.
Hepatitis C virus (HCV) encodes a single polyprotein, which is processed by cellular and viral proteases to generate 10 polypeptides. The HCV genome also contains an overlapping +1 reading frame that may lead to the synthesis of an additional protein. Until recently, studies of HCV have been hampered by the lack of a productive cell culture system. Since the identification of HCV genome approximately 17 years ago, structural, biochemical and biological information on HCV proteins has mainly been obtained with proteins produced by heterologous expression systems. In addition, some functional studies have also been confirmed with replicon systems or with retroviral particles pseudotyped with HCV envelope glycoproteins. The data that have accumulated on HCV proteins begin to provide a framework for understanding the molecular mechanisms involved in the major steps of HCV life cycle. Moreover, the knowledge accumulated on HCV proteins is also leading to the development of antiviral drugs among which some are showing promising results in early-phase clinical trials. This review summarizes the current knowledge on the functions and biochemical features of HCV proteins.
丙型肝炎病毒(HCV)编码一种单一的多聚蛋白,该多聚蛋白由细胞和病毒蛋白酶加工以产生10种多肽。HCV基因组还包含一个重叠的+1读码框,这可能导致另一种蛋白质的合成。直到最近,HCV的研究一直受到缺乏有效细胞培养系统的阻碍。自从大约17年前鉴定出HCV基因组以来,关于HCV蛋白的结构、生化和生物学信息主要是通过异源表达系统产生的蛋白获得的。此外,一些功能研究也已通过复制子系统或用HCV包膜糖蛋白假型化的逆转录病毒颗粒得到证实。积累的关于HCV蛋白的数据开始为理解HCV生命周期主要步骤中涉及的分子机制提供一个框架。此外,积累的关于HCV蛋白的知识也正在推动抗病毒药物的开发,其中一些药物在早期临床试验中显示出有希望的结果。本综述总结了目前关于HCV蛋白功能和生化特性的知识。