Structures of hepatitis C virus nonstructural proteins required for replicase assembly and function

被引:44
作者
Gu, Meigang [1 ]
Rice, Charles M. [1 ]
机构
[1] Rockefeller Univ, Lab Virol & Infect Dis, Ctr Study Hepatitis C, New York, NY 10065 USA
关键词
DEPENDENT RNA-POLYMERASE; NS3 PROTEASE DOMAIN; MEMBRANE ASSOCIATION; CRYSTAL-STRUCTURE; NS5A PROTEIN; PHOSPHORYLATION SITE; TRANSMEMBRANE DOMAIN; HELICASE ACTIVITY; HCV NS3; IDENTIFICATION;
D O I
10.1016/j.coviro.2013.03.013
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Approximately 3% of the world population is infected with hepatitis C virus (HCV), causing a serious public health burden. Like other positive-strand RNA viruses, HCV assembles replicase complexes in association with cellular membranes and produces progeny RNA genomes through negative-strand intermediates. The viral proteins required for RNA replication are nonstructural (NS) proteins NS3 to NS5B. Owing to many obstacles and limitations in structural characterization of proteins and complexes with multiple transmembrane segments, attempts to understand the assembly and action of the HCV replicase complex have been challenging. Nevertheless, great progress has been made in obtaining structural information for several replicase components, providing insights into some aspects of the viral genome replication machinery.
引用
收藏
页码:129 / 136
页数:8
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