Detection of Nonstructural Protein 6 in Murine Coronavirus-Infected Cells and Analysis of the Transmembrane Topology by Using Bioinformatics and Molecular Approaches

被引:41
作者
Baliji, Surendranath
Cammer, Stephen A. [2 ]
Sobral, Bruno [2 ]
Baker, Susan C. [1 ]
机构
[1] Loyola Univ, Med Ctr, Dept Microbiol & Immunol, Stritch Sch Med, Maywood, IL 60153 USA
[2] Virginia Polytech Inst & State Univ, Virginia Bioinformat Inst, Blacksburg, VA 24061 USA
关键词
MOUSE HEPATITIS-VIRUS; DOUBLE-MEMBRANE-VESICLES; PAPAIN-LIKE PROTEINASE; HYDROPHOBIC DOMAINS; 3C-LIKE PROTEINASE; CLEAVAGE SITE; REPLICATION; IDENTIFICATION; POLYPROTEIN; MHV-A59;
D O I
10.1128/JVI.00254-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Coronaviruses encode large replicase polyproteins which are proteolytically processed by viral proteases to generate mature nonstructural proteins (nsps) that form the viral replication complex. Mouse hepatitis virus (MHV) replicase products nsp3, nsp4, and nsp6 are predicted to act as membrane anchors during assembly of the viral replication complexes. We report the first antibody-mediated Western blot detection of nsp6 from MHV-infected cells. The nsp6-specific peptide antiserum detected the replicase intermediate p150 (nsp4 to nsp11) and two nsp6 products of approximately 23 and 25 kDa. Analysis of nsp6 transmembrane topology revealed six membrane-spanning segments and a conserved hydrophobic domain in the C-terminal cytosolic tail.
引用
收藏
页码:6957 / 6962
页数:6
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