Fluorescent lipid probes in the study of viral membrane fusion

被引:56
作者
Blumenthal, R
Gallo, SA
Viard, M
Raviv, Y
Puri, A
机构
[1] NCI, Lab Expt & Computat Biol, Ctr Canc Res, SAIC, Frederick, MD 21702 USA
[2] NCI, Intramural Res Support Program, SAIC, Frederick, MD 21701 USA
关键词
membrane fusion; HIV; influenza hemagglutinin; octadecyl rhodamine; photolabeling; fluorescence;
D O I
10.1016/S0009-3084(02)00019-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescent lipid probes are widely used in the observation of viral membrane fusion, providing a sensitive method to study fusion mechanism(s), Due to the wealth of data concerning liposome fusion, a variety of fusion assays has been designed including fluorescent probe redistribution, fluorescence dequenching, fluorescence resonance energy transfer and photosensitized labeling. These methods can be tailored for different virus fusion assays. For instance, virions can be loaded with membrane dye which dequenches at the moment of membrane merger. This allows for continuous observation of fusion and therefore kinetic information can be acquired, In the case of cells expressing viral envelope proteins, dye redistribution studies of lipidic and water-soluble fluorophores yield information about fusion intermediates. Lipid probes can be metabolically incorporated into cell membranes, allowing observation of membrane fusion in vitro with minimal chance of flip flop, non-specific transfer and formation of microcrystals. Fluorescent lipid probes have been incorporated into liposomes and;;or reconstituted viral envelopes, which provide a well-defined membrane environment for fusion to occur. Interactions of the viral fusion machinery with the membrane can be observed through the photosensitized labeling of the interacting segments of envelope proteins with a hydrophobic probe. Thus, fluorescent lipid probes provide a broad repertoire of fusion assays and powerful tools to produce precise, quantitative data in real time required for the elucidation of the complex process of viral fusion. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:39 / 55
页数:17
相关论文
共 73 条
[1]  
AROETI B, 1991, J BIOL CHEM, V266, P15845
[2]  
AROETI B, 1992, J BIOL CHEM, V267, P13272
[3]   5-[I-125]IODONAPHTHYL AZIDE, A REAGENT TO DETERMINE PENETRATION OF PROTEINS INTO LIPID BILAYER OF BIOLOGICAL-MEMBRANES [J].
BERCOVICI, T ;
GITLER, C .
BIOCHEMISTRY, 1978, 17 (08) :1484-1489
[4]  
BLUMENTHAL R, 1987, J BIOL CHEM, V262, P13614
[5]   Dilation of the influenza hemagglutinin fusion pore revealed by the kinetics of individual cell-cell fusion events [J].
Blumenthal, R ;
Sarkar, DP ;
Durell, S ;
Howard, DE ;
Morris, SJ .
JOURNAL OF CELL BIOLOGY, 1996, 135 (01) :63-71
[6]   The influenza haemagglutinin-induced fusion cascade: effects of target membrane permeability changes [J].
Blumenthal, R ;
Morris, SJ .
MOLECULAR MEMBRANE BIOLOGY, 1999, 16 (01) :43-47
[7]   FUSOGENIC SELECTIVITY OF THE ENVELOPE GLYCOPROTEIN IS A MAJOR DETERMINANT OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 TROPISM FOR CD4(+) T-CELL LINES VS PRIMARY MACROPHAGES [J].
BRODER, CC ;
BERGER, EA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (19) :9004-9008
[8]   FUSION BETWEEN SENDAI VIRUS ENVELOPES AND BIOLOGICAL-MEMBRANES AS MONITORED BY ENERGY-TRANSFER METHODS [J].
CHEJANOVSKY, N ;
EYTAN, GD ;
LOYTER, A .
FEBS LETTERS, 1984, 174 (02) :304-309
[9]  
CHERNOMORDIK L, 1995, J MEMBRANE BIOL, V146, P1
[10]   The pathway of membrane fusion catalyzed by influenza hemagglutinin: Restriction of lipids, hemifusion, and lipidic fusion pore formation [J].
Chernomordik, LV ;
Frolov, VA ;
Leikina, E ;
Bronk, P ;
Zimmerberg, J .
JOURNAL OF CELL BIOLOGY, 1998, 140 (06) :1369-1382