Membrane permeability changes at early stages of influenza hemagglutinin-mediated fusion

被引:67
作者
Frolov, VA
Dunina-Barkovskaya, AY
Samsonov, AV
Zimmerberg, J
机构
[1] NICHHD, Lab Cellular & Mol Biophys, NIH, Bethesda, MD 20892 USA
[2] Russian Acad Sci, AN Frumkin Inst Electrochem, Moscow, Russia
[3] Moscow MV Lomonosov State Univ, AN Belozersky Inst Physicochem Biol, Moscow, Russia
关键词
D O I
10.1016/S0006-3495(03)74602-5
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
While biological membrane fusion is classically defined as the leak-free merger of membranes and contents, leakage is a finding in both experimental and theoretical studies. The fusion stages, if any, that allow membrane permeation are uncharted. In this study we monitored membrane ionic permeability at early stages of fusion mediated by the fusogenic protein influenza hemagglutinin (HA). HAb2 cells, expressing HA on their plasma membrane, fused with human red blood cells, cultured liver cells PLC/PRF/5, or planar phospholipid bilayer membranes. With a probability that depended upon the target membrane, an increase of the electrical conductance of the fusing membranes (leakage) by up to several nS was generally detected. This leakage was recorded at the initial stages of fusion, when fusion pores formed. This leakage usually accompanied the "flickering'' stage of the early fusion pore development. As the pore widened, the leakage reduced; concomitantly, the lipid exchange between the fusing membranes accelerated. We conclude that during fusion pore formation, HA locally and temporarily increases the permeability of fusing membranes. Subsequent rearrangement in the fusion complex leads to the resealing of the leaky membranes and enlargement of the pore.
引用
收藏
页码:1725 / 1733
页数:9
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共 50 条
[1]   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
[2]   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
[3]   Membrane perturbation and fusion pore formation in influenza hemagglutinin-mediated membrane fusion - A new model for fusion [J].
Bonnafous, P ;
Stegmann, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (09) :6160-6166
[4]   ARREST OF MEMBRANE-FUSION EVENTS IN MAST-CELLS BY QUICK-FREEZING [J].
CHANDLER, DE ;
HEUSER, JE .
JOURNAL OF CELL BIOLOGY, 1980, 86 (02) :666-674
[5]  
CHERNOMORDIK L, 1995, J MEMBRANE BIOL, V146, P1
[6]   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
[7]  
Chernomordik LV, 1999, MOL MEMBR BIOL, V16, P33
[8]   Membrane mechanics can account for fusion pore dilation in stages [J].
Chizmadzhev, YA ;
Cohen, FS ;
Shcherbakov, A ;
Zimmerberg, J .
BIOPHYSICAL JOURNAL, 1995, 69 (06) :2489-2500
[9]   Methodologies in the study of cell-cell fusion [J].
Cohen, FS ;
Melikyan, GB .
METHODS, 1998, 16 (02) :215-226
[10]   Structural study of the relationship between the rate of membrane fusion and the ability of the fusion peptide of influenza virus to perturb bilayers [J].
Colotto, A ;
Epand, RM .
BIOCHEMISTRY, 1997, 36 (25) :7644-7651