Stegmann T, Schoen P, Bron R, Wey J, Bartoldus I, Ortiz A, Nieva J L, Wilschut J
Department of Biophysical Chemistry, University of Basel, Switzerland.
Biochemistry. 1993 Oct 26;32(42):11330-7. doi: 10.1021/bi00093a009.
Membrane fusion, in particular the fusion of enveloped viruses, is often measured with an assay based on octadecylrhodamine (R18) fluorescence dequenching. We have studied the association of R18 with membranes and used the R18 assay to measure virus fusion in model systems and in cultured cells. The results were compared with those of an assay based on the decrease in excimer fluorescence of pyrene-labeled phospholipids. For liposomes made from premixed R18 and phosphatidylcholine (PC), R18 fluorescence quenching was proportional to the concentration of the probe up to about 4 mol %. No quenching was found at very low concentrations of R18. However, various artificial and biological membranes labeled by the addition of R18 from an ethanolic solution showed significant quenching at such low R18 concentrations. Thus, some of the R18 was not randomly distributed but likely was associated with the surface of the membranes in the form of highly quenched clusters or micelles. Moreover, in influenza virus membranes, R18 appeared highly quenched at very low concentrations, indicative of the probe interacting with viral proteins. In contrast, pyrene-labeled PC incorporated in either liposomes or reconstituted viral membranes (virosomes) showed an excimer/monomer fluorescence ratio proportional to the concentration of probe. When intracellular membrane fusion was investigated with R18-labeled influenza virus or Semliki Forest virus (SFV), fluorescence dequenching was observed in the absence of fusion, most likely due to spontaneous probe exchange.(ABSTRACT TRUNCATED AT 250 WORDS)
膜融合,特别是包膜病毒的融合,通常采用基于十八烷基罗丹明(R18)荧光猝灭的检测方法来测定。我们研究了R18与膜的结合情况,并利用R18检测法在模型系统和培养细胞中测量病毒融合。将结果与基于芘标记磷脂的准分子荧光降低的检测方法所得结果进行了比较。对于由预混合的R18和磷脂酰胆碱(PC)制成的脂质体,R18荧光猝灭与探针浓度成正比,直至约4摩尔%。在R18浓度非常低时未发现猝灭现象。然而,通过从乙醇溶液中添加R18标记的各种人工膜和生物膜在如此低的R18浓度下显示出显著的猝灭。因此,一些R18并非随机分布,而是可能以高度猝灭的簇或胶束形式与膜表面结合。此外,在流感病毒膜中,R18在非常低的浓度下就呈现出高度猝灭,这表明探针与病毒蛋白相互作用。相比之下,掺入脂质体或重组病毒膜(病毒体)中的芘标记PC显示准分子/单体荧光比率与探针浓度成正比。当用R18标记的流感病毒或Semliki森林病毒(SFV)研究细胞内膜融合时,在没有融合的情况下观察到荧光猝灭,这很可能是由于探针的自发交换所致。(摘要截短于250字)