Interaction of hepatitis C virus proteins with host cell membranes and lipids

被引:110
作者
Dubuisson, J
Penin, F
Moradpour, D
机构
[1] Inst Biol Lille, CNRS, UPR 2511, F-59021 Lille, France
[2] Inst Pasteur, F-59021 Lille, France
[3] Inst Biol & Chim Prot, CNRS, UMR 5086, F-69367 Lyon 07, France
[4] Univ Freiburg, Dept Med 2, D-79106 Freiburg, Germany
关键词
D O I
10.1016/S0962-8924(02)02383-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
For replication, viruses depend on specific components and energy supplies from the host cell. The main steps in the lifecycle of positive-strand RNA viruses depend on cellular membranes. Interest is increasing in studying the interactions between host cell membranes and viral proteins to understand how such viruses replicate their genome and produce infectious particles. These studies should also lead to a better knowledge of the different mechanisms underlying membrane-protein associations. The various molecular interactions of hepatitis C virus proteins with the membranes and lipids of the infected cell highlight how a virus can exploit the diversity of interactions that occur between proteins and membranes or lipid structures.
引用
收藏
页码:517 / 523
页数:7
相关论文
共 63 条
[1]   Characterization of low- and very-low-density hepatitis C virus RNA-containing particles [J].
André, P ;
Komurian-Pradel, F ;
Deforges, S ;
Perret, M ;
Berland, JL ;
Sodoyer, M ;
Pol, S ;
Bréchot, C ;
Paranhos-Baccalà, G ;
Lotteau, V .
JOURNAL OF VIROLOGY, 2002, 76 (14) :6919-6928
[2]  
[Anonymous], FIELDS VIROLOGY
[3]   Hepatitis C virus core protein shows a cytoplasmic localization and associates to cellular lipid storage droplets [J].
Barba, G ;
Harper, F ;
Harada, T ;
Kohara, M ;
Goulinet, S ;
Matsuura, Y ;
Eder, G ;
Schaff, Z ;
Chapman, MJ ;
Miyamura, T ;
Brechot, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (04) :1200-1205
[4]   Novel cell culture systems for the hepatitis C virus [J].
Bartenschlager, R ;
Lohmann, V .
ANTIVIRAL RESEARCH, 2001, 52 (01) :1-17
[5]   STRUCTURAL AND FUNCTIONAL-CHARACTERIZATION OF THE POLIOVIRUS REPLICATION COMPLEX [J].
BIENZ, K ;
EGGER, D ;
PFISTER, T ;
TROXLER, M .
JOURNAL OF VIROLOGY, 1992, 66 (05) :2740-2747
[6]   Efficient initiation of HCV RNA replication in cell culture [J].
Blight, KJ ;
Kolykhalov, AA ;
Rice, CM .
SCIENCE, 2000, 290 (5498) :1972-1974
[7]   INTRACELLULAR PROTEIN TOPOGENESIS [J].
BLOBEL, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (03) :1496-1500
[8]   An amino-terminal amphipathic α-helix mediates membrane association of the hepatitis C virus nonstructural protein 5A [J].
Brass, V ;
Bieck, E ;
Montserret, R ;
Wölk, B ;
Hellings, JA ;
Blum, HE ;
Penin, F ;
Moradpour, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (10) :8130-8139
[9]   Subcellular localization and topology of the p7 polypeptide of hepatitis C virus [J].
Carrère-Kremer, S ;
Montpellier-Pala, C ;
Cocquerel, L ;
Wychowski, C ;
Penin, F ;
Dubuisson, J .
JOURNAL OF VIROLOGY, 2002, 76 (08) :3720-3730
[10]   Charged residues in the transmembrane domains of hepatitis C virus glycoproteins play a major role in the processing, subcellular localization, and assembly of these envelope proteins [J].
Cocquerel, L ;
Wychowski, C ;
Minner, F ;
Penin, F ;
Dubuisson, J .
JOURNAL OF VIROLOGY, 2000, 74 (08) :3623-3633