Mechanisms of enveloped virus entry into animal cells

被引:65
作者
Klasse, PJ
Bron, R
Marsh, M
机构
[1] UCL, MRC, Mol Cell Biol Lab, London WC1E 6BT, England
[2] UCL, Dept Biochem & Mol Biol, London WC1E 6BT, England
基金
英国医学研究理事会;
关键词
endocytosis; enveloped viruses; membrane fusion; virus entry; viruses; virus fusion; virus receptors;
D O I
10.1016/S0169-409X(98)00002-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The ability of viruses to transfer macromolecules between cells makes them attractive starting points for the design of biological delivery vehicles. Virus-based vectors and sub-viral systems are already finding biotechnological and medical applications for gene, peptide, vaccine and drug delivery. Progress has been made in understanding the cellular and molecular mechanisms underlying virus entry, particularly in identifying virus receptors. However, receptor binding is only a first step and we now have to understand how these molecules facilitate entry, how enveloped viruses fuse with cells or non-enveloped viruses penetrate the cell membrane, and what happens following penetration. Only through these detailed analyses will the full potential of viruses as vectors and delivery vehicles be realised. Here we discuss aspects of the entry mechanisms for several well-characterised viral systems. We do not attempt to provide a fully comprehensive review of virus entry but focus primarily on enveloped viruses. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:65 / 91
页数:27
相关论文
共 260 条
[1]   HIV-1 PROTEASE CLEAVES ACTIN DURING ACUTE INFECTION OF HUMAN LYMPHOCYTES-T [J].
ADAMS, LD ;
TOMASSELLI, AG ;
ROBBINS, P ;
MOSS, B ;
HEINRIKSON, RL .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1992, 8 (02) :291-295
[2]   A PUTATIVE MURINE ECOTROPIC RETROVIRUS RECEPTOR GENE ENCODES A MULTIPLE MEMBRANE-SPANNING PROTEIN AND CONFERS SUSCEPTIBILITY TO VIRUS-INFECTION [J].
ALBRITTON, LM ;
TSENG, L ;
SCADDEN, D ;
CUNNINGHAM, JM .
CELL, 1989, 57 (04) :659-666
[3]   OLIGOMERIC REARRANGEMENT OF TICK-BORNE ENCEPHALITIS-VIRUS ENVELOPE PROTEINS INDUCED BY AN ACIDIC PH [J].
ALLISON, SL ;
SCHALICH, J ;
STIASNY, K ;
MANDL, CW ;
KUNZ, C ;
HEINZ, FX .
JOURNAL OF VIROLOGY, 1995, 69 (02) :695-700
[4]   RETROVIRUS-INDUCED CELL-FUSION IS ENHANCED BY PROTEASE TREATMENT [J].
ANDERSEN, KB ;
SKOV, H .
JOURNAL OF GENERAL VIROLOGY, 1989, 70 :1921-1927
[5]   Bound simian virus 40 translocates to caveolin-enriched membrane domains, and its entry is inhibited by drugs that selectively disrupt caveolae [J].
Anderson, HA ;
Chen, YZ ;
Norkin, LC .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (11) :1825-1834
[6]  
Anderson Richard G., 1993, Trends in Cell Biology, V3, P69, DOI 10.1016/0962-8924(93)90065-9
[7]   HUMAN GENE-THERAPY [J].
ANDERSON, WF .
SCIENCE, 1992, 256 (5058) :808-813
[8]   PROTEIN-PROTEIN INTERACTIONS IN AN ALPHAVIRUS MEMBRANE [J].
ANTHONY, RP ;
BROWN, DT .
JOURNAL OF VIROLOGY, 1991, 65 (03) :1187-1194
[9]   CELLULAR PROTEINS BOUND TO IMMUNODEFICIENCY VIRUSES - IMPLICATIONS FOR PATHOGENESIS AND VACCINES [J].
ARTHUR, LO ;
BESS, JW ;
SOWDER, RC ;
BENVENISTE, RE ;
MANN, DL ;
CHERMANN, JC ;
HENDERSON, LE .
SCIENCE, 1992, 258 (5090) :1935-1938
[10]   HUMAN-IMMUNODEFICIENCY-VIRUS ENVELOPE GLYCOPROTEIN CD4-MEDIATED FUSION OF NONPRIMATE CELLS WITH HUMAN-CELLS [J].
ASHORN, PA ;
BERGER, EA ;
MOSS, B .
JOURNAL OF VIROLOGY, 1990, 64 (05) :2149-2156