In trans interaction of hepatitis C virus helicase domains mediates protease activity critical for internal NS3 cleavage and cell transformation

被引:5
作者
Pan, Ren-You [1 ]
Hung, Tzu-Min [2 ]
Kou, Yi-Hen [1 ]
Chan, Nei-Li [2 ]
Chang, Ming-Fu [2 ]
Chang, Shin C. [1 ]
机构
[1] Natl Taiwan Univ, Coll Med, Inst Microbiol, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Coll Med, Inst Biochem & Mol Biol, Taipei 100, Taiwan
来源
FEBS LETTERS | 2010年 / 584卷 / 03期
关键词
Hepatitis C virus; Internal NS3 cleavage; In trans interaction; NS3; helicase; NS3 serine protease; Polyprotein processing; Transforming activity; CRYSTAL-STRUCTURE; RNA HELICASE; PROTEINASE; NS4A;
D O I
10.1016/j.febslet.2009.11.090
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatitis C virus (HCV) internal non-structural protein 3 (NS3) cleavage can occur in trans in the presence of NS4A. In this study, we have further demonstrated a critical role of the helicase domain in the internal NS3 cleavage, different from HCV polyprotein processing which requires only the serine protease domain. The NTPase domain of NS3 helicase interacts with the RNA binding domain to facilitate internal NS3 cleavage. In addition, NS3 protease activity contributes to the transforming ability of the major internal cleavage product NS3(1-402). These findings imply important roles of the internal cleavage and protease activity of the NS3 protein in the pathogenesis of HCV.
引用
收藏
页码:482 / 486
页数:5
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