Structure of Hepatitis E Virion-sized Particle Reveals an RNA-dependent Viral Assembly Pathway

被引:123
作者
Xing, Li [2 ]
Li, Tian-Cheng [3 ]
Mayazaki, Naoyuki [2 ]
Simon, Martha N. [4 ]
Wall, Joseph S. [4 ]
Moore, Mary
Wang, Che-Yen
Takeda, Naokazu [3 ]
Wakita, Takaji [3 ]
Miyamura, Tatsuo [3 ]
Cheng, R. Holland [1 ]
机构
[1] Univ Calif Davis, Dept Mol & Cellular Biol, Davis, CA 95616 USA
[2] Huddinge Univ Hosp, Karolinska Inst, Struct Virol Sect, SE-14186 Stockholm, Sweden
[3] Natl Inst Infect Dis, Dept Virol 2, Tokyo 2080011, Japan
[4] Brookhaven Natl Lab, Dept Biol, Upton, NY 11973 USA
基金
瑞典研究理事会; 美国国家卫生研究院;
关键词
VIRUS-LIKE PARTICLES; CAPSID PROTEIN; HEV; INFECTION; PROGRAM;
D O I
10.1074/jbc.M110.106336
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 E virus (HEV) induces acute hepatitis in humans with a high fatality rate in pregnant women. There is a need for anti-HEV research to understand the assembly process of HEV native capsid. Here, we produced a large virion-sized and a small T=1 capsid by expressing the HEV capsid protein in insect cells with and without the N-terminal 111 residues, respectively, for comparative structural analysis. The virion-sized capsid demonstrates a T=3 icosahedral lattice and contains RNA fragment in contrast to the RNA-free T= 1 capsid. However, both capsids shared common decameric organization. The in vitro assembly further demonstrated that HEV capsid protein had the intrinsic ability to form decameric intermediate. Our data suggest that RNA binding is the extrinsic factor essential for the assembly of HEV native capsids.
引用
收藏
页码:33175 / 33183
页数:9
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