The hepatitis C viral NS3 protein is a processive DNA helicase with cofactor enhanced RNA unwinding

被引:184
作者
Pang, PS
Jankowsky, E
Planet, PJ
Pyle, AM
机构
[1] Columbia Univ, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Med Scientist Training Program, New York, NY 10032 USA
[3] Case Western Reserve Univ, Sch Med, Dept Biochem, Cleveland, OH 44106 USA
[4] Columbia Univ, Integrated Program Cellular Mol & Biophys Sci, New York, NY USA
[5] Columbia Univ, Howard Hughes Med Inst, New York, NY 10032 USA
关键词
DExH/D; helicase; hepatitis C; NS3; NS4A;
D O I
10.1093/emboj/21.5.1168
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
The RNA helicase/protease NS3 plays a central role in the RNA replication of hepatitis C virus (HCV), a cytoplasmic PUNA virus that represents a major worldwide health problem. NS3 is, therefore, an important drug target in the effort to combat HCV. Most work has focused on the protease, rather than the helicase, activities of the enzyme. In order to further characterize NS3 helicase activity, we evaluated individual stages of duplex unwinding by NS3 alone and in complex with cofactor NS4A. Despite a putative replicative role in RNA unwinding, we found that NS3 alone is a surprisingly poor helicase on RNA, but that RNA activity is promoted by cofactor NS4A. In contrast, NS3 alone is a highly processive helicase on DNA. Phylogenetic analysis suggests that this robust DNA helicase activity is not vestigial and may have specifically evolved in HCV. Given that HCV has no replicative DNA intermediate, these findings suggest that NS3 may have the capacity to affect host DNA.
引用
收藏
页码:1168 / 1176
页数:9
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