Role of the N-terminal peptides of viral envelope proteins in membrane fusion

被引:38
作者
Martin, I
Ruysschaert, JM
Epand, RM
机构
[1] McMaster Univ, Hlth Sci Ctr, Dept Biochem, Hamilton, ON L8N 3Z5, Canada
[2] Free Univ Brussels, LCPMI CP 206 2, B-1050 Brussels, Belgium
关键词
viral fusion peptide; model membrane; fusogenic activity; secondary structure; orientation; hexagonal phase;
D O I
10.1016/S0169-409X(99)00031-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Membrane fusion is an important biological process that is observed in a wide variety of intra and intercellular events. In this review, work done in the last few years on the molecular mechanism of viral membrane fusion is highlighted, focusing in particular on the role of the fusion peptide and the modification of the lipid bilayer structure. While the Influenza hemagglutinin is currently the best understand fusion protein, there is still much to be learned about the key events in enveloped virus fusion reactions. This review compares our current understanding of the membrane fusion activity of Influenza and retrovirus viruses. We shall be concerned especially with the studies that lead to interpretations at the molecular level, so we shall concentrate on model membrane systems where the molecular components of the membrane and the environment are strictly controlled. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:233 / 255
页数:23
相关论文
共 173 条
[31]   Mutational analysis of the fusion peptide of the human immunodeficiency virus type 1: Identification of critical glycine residues [J].
Delahunty, MD ;
Rhee, I ;
Freed, EO ;
Bonifacino, JS .
VIROLOGY, 1996, 218 (01) :94-102
[32]   SPC3, a V3 loop-derived synthetic peptide inhibitor of HIV-1 infection, binds to cell surface glycosphingolipids [J].
Delezay, O ;
Hammache, D ;
Fantini, J ;
Yahi, N .
BIOCHEMISTRY, 1996, 35 (49) :15663-15671
[33]  
DELIMA MCP, 1995, BBA-BIOMEMBRANES, V1236, P323
[34]   HIV-1 entry into CD4(+) cells is mediated by the chemokine receptor CC-CKR-5 [J].
Dragic, T ;
Litwin, V ;
Allaway, GP ;
Martin, SR ;
Huang, YX ;
Nagashima, KA ;
Cayanan, C ;
Maddon, PJ ;
Koup, RA ;
Moore, JP ;
Paxton, WA .
NATURE, 1996, 381 (6584) :667-673
[35]   PHOTOLABELING IDENTIFIES A PUTATIVE FUSION DOMAIN IN THE ENVELOPE GLYCOPROTEIN OF RABIES AND VESICULAR STOMATITIS VIRUSES [J].
DURRER, P ;
GAUDIN, Y ;
RUIGROK, RWH ;
GRAF, R ;
BRUNNER, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (29) :17575-17581
[36]   MEMBRANE DESTABILIZATION BY N-TERMINAL PEPTIDES OF VIRAL ENVELOPE PROTEINS [J].
DUZGUNES, N ;
SHAVNIN, SA .
JOURNAL OF MEMBRANE BIOLOGY, 1992, 128 (01) :71-80
[37]   THE HYDROPHOBIC MOMENT DETECTS PERIODICITY IN PROTEIN HYDROPHOBICITY [J].
EISENBERG, D ;
WEISS, RM ;
TERWILLIGER, TC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (01) :140-144
[38]   H+-INDUCED AND CA-2+-INDUCED FUSION AND DESTABILIZATION OF LIPOSOMES [J].
ELLENS, H ;
BENTZ, J ;
SZOKA, FC .
BIOCHEMISTRY, 1985, 24 (13) :3099-3106
[39]   FUSION OF INFLUENZA HEMAGGLUTININ-EXPRESSING FIBROBLASTS WITH GLYCOPHORIN-BEARING LIPOSOMES - ROLE OF HEMAGGLUTININ SURFACE-DENSITY [J].
ELLENS, H ;
BENTZ, J ;
MASON, D ;
ZHANG, F ;
WHITE, JM .
BIOCHEMISTRY, 1990, 29 (41) :9697-9707
[40]   MEMBRANE ORIENTATION OF THE SIV FUSION PEPTIDE DETERMINES ITS EFFECT ON BILAYER STABILITY AND ABILITY TO PROMOTE MEMBRANE-FUSION [J].
EPAND, RF ;
MARTIN, I ;
RUYSSCHAERT, JM ;
EPAND, RM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 205 (03) :1938-1943