Ohki S, Zschörnig O
Department of Biophysical Sciences, State University of New York at Buffalo 14214.
Chem Phys Lipids. 1993 Oct;65(3):193-204. doi: 10.1016/0009-3084(93)90017-w.
Divalent cation (Ca2+ and Mg2+) and hydrogen ion-induced fusions of small unilamellar phosphatidic acid vesicles were studied by the use of fluorescence fusion assay. These fusogenic ions also increased interfacial tension and reduced the surface dielectric constant of phosphatidic acid membranes as the ion concentration increased. A good correlation was found between the threshold of vesicle fusion and the degree of changes in such membrane properties induced by these fusogenic ions. At the fusion threshold point, the increase in interfacial tension and the decreased surface dielectric constant of the membrane were approximately 6 and 14 dyn/cm, respectively, regardless of Ca2+, Mg2+ or H+. Such changes correspond to the increases in surface hydrophobicity of the membrane. As these fusogenic ionic concentrations increased, the electrophoretic mobility of the phosphatidic acid vesicle decreased, because of the binding of ions to negatively charged sites of the membranes. However, the quantities of the reduced negative surface charges were not necessarily in good correlation with the threshold of vesicle fusion. It is suggested that the complexes of the phosphate group with these fusogenic ions are responsible for increases in the surface hydrophobicity of the membrane, which is an important factor for membrane fusion.
利用荧光融合分析法研究了二价阳离子(Ca2+和Mg2+)以及氢离子诱导的小单层磷脂酸囊泡融合。随着离子浓度的增加,这些促融合离子还会增加界面张力并降低磷脂酸膜的表面介电常数。在囊泡融合阈值与这些促融合离子引起的此类膜性质变化程度之间发现了良好的相关性。在融合阈值点,无论Ca2+、Mg2+还是H+,膜的界面张力增加和表面介电常数降低分别约为6和14达因/厘米。此类变化对应于膜表面疏水性的增加。随着这些促融合离子浓度的增加,磷脂酸囊泡的电泳迁移率降低,这是由于离子与膜的带负电位点结合。然而,表面负电荷减少的量与囊泡融合阈值不一定有良好的相关性。有人提出,磷酸基团与这些促融合离子的复合物导致膜表面疏水性增加,这是膜融合的一个重要因素。