Flavivirus structure and membrane fusion

被引:112
作者
Heinz, FX [1 ]
Allison, SL [1 ]
机构
[1] Univ Vienna, Inst Virol, A-1095 Vienna, Austria
来源
FLAVIVIRUSES: STRUCTURE, REPLICATION AND EVOLUTION | 2003年 / 59卷
关键词
D O I
10.1016/S0065-3527(03)59003-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Flaviviruses are spherical enveloped viruses with a diameter of approximately 50 nm that contain only three structural proteins: E (envelope), prM/M (membrane), and C (capsid). This chapter focuses primarily on structural aspects of the envelope glycoproteins, their organization in the viral envelope, and the mechanism of virus-induced membrane fusion. Significant progress has been made toward the understanding of the structure and organization of the flavivirus virion. The current view of the flavivirus life cycle, including entry, assembly, maturation, and release suggests that virus entry occurs by receptor-mediated endocytosis, and the acidic pH in the endosome triggers structural alterations in the E protein that lead to the fusion of the viral membrane with the endosomal membrane and the release of the nucleocapsid. During assembly, immature prM-containing virions are believed to be formed in the endoplasmic reticulum (ER) and transported through the secretory pathway of the cell. The most important structural features revealed by current studies are: an icosahedral arrangement of the envelope proteins and a characteristic envelope protein structure, which, together with the alphavirus E1 protein, defines a separate class of viral fusion protein.
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页码:63 / +
页数:43
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共 106 条
[11]   Oligomeric structure of virion-associated and soluble forms of the simian immunodeficiency virus envelope protein in the prefusion activated conformation [J].
Center, RJ ;
Schuck, P ;
Leapman, RD ;
Arthur, LO ;
Earl, PL ;
Moss, B ;
Lebowitz, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (26) :14877-14882
[12]   West Nile virus envelope proteins: nucleotide sequence analysis of strains differing in mouse neuroinvasiveness [J].
Chambers, TJ ;
Halevy, M ;
Nestorowicz, A ;
Rice, CM ;
Lustig, S .
JOURNAL OF GENERAL VIROLOGY, 1998, 79 :2375-2380
[13]   A single intramuscular injection of recombinant plasmid DNA induces protective immunity and prevents Japanese encephalitis in mice [J].
Chang, GJJ ;
Hunt, AR ;
Davis, B .
JOURNAL OF VIROLOGY, 2000, 74 (09) :4244-4252
[14]   Dengue virus infectivity depends on envelope protein binding to target cell heparan sulfate [J].
Chen, YP ;
Maguire, T ;
Hileman, RE ;
Fromm, JR ;
Esko, JD ;
Linhardt, RJ ;
Marks, RM .
NATURE MEDICINE, 1997, 3 (08) :866-871
[15]   Molecular aspects of the endocytic pathway [J].
Clague, MJ .
BIOCHEMICAL JOURNAL, 1998, 336 :271-282
[16]   TECHNIQUES FOR HEMAGGLUTINATION AND HEMAGGLUTINATION-INHIBITION WITH ARTHROPOD-BORNE VIRUSES [J].
CLARKE, DH ;
CASALS, J .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1958, 7 (05) :561-573
[17]   Membrane fusion activity of tick-borne encephalitis virus and recombinant subviral particles in a liposomal model system [J].
Corver, J ;
Ortiz, A ;
Allison, SL ;
Schalich, J ;
Heinz, FX ;
Wilschut, J .
VIROLOGY, 2000, 269 (01) :37-46
[18]   α-glucosidase inhibitors reduce dengue virus production by affecting the initial steps of virion morphogenesis in the endoplasmic reticulum [J].
Courageot, MP ;
Frenkiel, MP ;
Santos, CDD ;
Deubel, V ;
Desprès, P .
JOURNAL OF VIROLOGY, 2000, 74 (01) :564-572
[19]   Monoclonal antibodies that bind to domain III of dengue virus E glycoprotein are the most efficient blockers of virus adsorption to Vero cells [J].
Crill, WD ;
Roehrig, JT .
JOURNAL OF VIROLOGY, 2001, 75 (16) :7769-7773
[20]   West Nile virus recombinant DNA vaccine protects mouse and horse from virus challenge and expresses in vitro a noninfectious recombinant antigen that can be used in enzyme-linked immunosorbent assays [J].
Davis, BS ;
Chang, GJJ ;
Cropp, B ;
Roehrig, JT ;
Martin, DA ;
Mitchell, CJ ;
Bowen, R ;
Bunning, ML .
JOURNAL OF VIROLOGY, 2001, 75 (09) :4040-4047