Fusion activity of the influenza virus hemagglutinin does not require a transbilayer pH gradient

被引:0
|
作者
RamalhoSantos, J
deLima, MCP
机构
[1] UNIV COIMBRA,DEPT BIOCHEM,P-3000 COIMBRA,PORTUGAL
[2] UNIV COIMBRA,DEPT ZOOL,P-3000 COIMBRA,PORTUGAL
来源
关键词
influenza virus hemagglutinin; pH gradient; liposome; erythrocyte ghost;
D O I
10.1016/S0005-2736(97)00166-1
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
Following reports suggesting that membrane fusion mediated by the influenza virus hemagglutinin might be dependent on a pH gradient across a putative target membrane, we have designed experiments in which this issue could be addressed directly. Accordingly, we have prepared two populations of liposomes, both simulating the plasma membrane of target cells, but with the pH of the internal aqueous medium buffered either at pH 7.4 (physiological cytosol pH) or pH 5.0 (endosomal pH at which influenza virus displays maximal fusion activity). Monitoring fusion as the relief in self-quenching of the fluorescent probe octadecylrhodamine B chloride we have found that the internal pH of the target liposomes did not influence membrane merging as mediated by the influenza virus hemagglutinin, thus demonstrating that a transmembrane pH gradient is not required for the fusion process to take place. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:194 / 198
页数:5
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