Severe Acute Respiratory Syndrome Coronavirus Nonstructural Protein 2 Interacts with a Host Protein Complex Involved in Mitochondrial Biogenesis and Intracellular Signaling

被引:170
|
作者
Cornillez-Ty, Cromwell T. [3 ,4 ]
Liao, Lujian [4 ]
Yates, John R., III [4 ]
Kuhn, Peter [4 ]
Buchmeier, Michael J. [1 ,2 ,3 ]
机构
[1] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Med, Div Infect Dis, Irvine, CA 92697 USA
[3] Scripps Res Inst, Mol & Integrat Neurosci Dept, La Jolla, CA 92037 USA
[4] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
MURINE HEPATITIS-VIRUS; SARS CORONAVIRUS; IDENTIFICATION TECHNOLOGY; CRYSTAL-STRUCTURE; ENDORIBONUCLEASE; PROHIBITIN; NSP15; EXORIBONUCLEASE; TRANSCRIPTION; REPLICATION;
D O I
10.1128/JVI.00842-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The severe acute respiratory syndrome coronavirus (SARS-CoV) generates 16 nonstructural proteins (nsp's) through proteolytic cleavage of a large precursor protein. Although several nsp's exhibit catalytic activities that are important for viral replication and transcription, other nsp's have less clearly defined roles during an infection. In order to gain a better understanding of their functions, we attempted to identify host proteins that interact with nsp's during SARS-CoV infections. For nsp2, we identified an interaction with two host proteins, prohibitin 1 (PHB1) and PHB2. Our results suggest that nsp2 may be involved in the disruption of intracellular host signaling during SARS-CoV infections.
引用
收藏
页码:10314 / 10318
页数:5
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