Ohki S
Biochim Biophys Acta. 1982 Jul 14;689(1):1-11. doi: 10.1016/0005-2736(82)90182-1.
A mechanism for the divalent cation-induced membrane fusion of phosphatidylserine membranes is proposed. Fusion was followed by the Tb/DPA (dipicolinic acid) assay, monitoring the fluorescent intensity for mixing of the internal aqueous contents of unilamellar lipid vesicles, and the threshold concentrations required for various divalent cations to induce membrane fusion were determined from the fluorescence spectrum of the lipid vesicle suspension with respect to various concentrations of divalent ions. Also, the surface tension of monolayers made of the same lipids as used in the fusion experiments was measured with respect to the variation of divalent cation concentrations. The surface tension increase in the monolayer, induced by changing divalent ion concentrations from zero to a concentration which corresponded to its threshold concentration to induce vesicle membrane fusion, was the same (approx. 8 dyn/cm) for all divalent ions used. From these experimental data and theory concerning ion binding to the membrane, it is deduced that the main cause of divalent cation-induced membrane fusion of phosphatidylserine membranes is the degree of increased hydrophobicity (surface tension increase) of the membrane surface, which results from the binding of cations to acidic phospholipid membrane surfaces. Some discussion on the molecular mechanism of phospholipid membrane fusion is given.
提出了一种二价阳离子诱导磷脂酰丝氨酸膜融合的机制。融合过程通过Tb/DPA(二吡啶甲酸)测定法进行监测,该方法通过监测单层脂质囊泡内部水相内容物混合时的荧光强度来跟踪融合情况,并根据脂质囊泡悬浮液相对于各种二价离子浓度的荧光光谱确定各种二价阳离子诱导膜融合所需的阈值浓度。此外,还测量了与融合实验中使用的相同脂质制成的单层膜在二价阳离子浓度变化时的表面张力。对于所有使用的二价离子,当二价离子浓度从零变化到对应于其诱导囊泡膜融合的阈值浓度时,单层膜表面张力的增加是相同的(约8达因/厘米)。根据这些实验数据以及关于离子与膜结合的理论,可以推断出二价阳离子诱导磷脂酰丝氨酸膜融合的主要原因是阳离子与酸性磷脂膜表面结合导致膜表面疏水性增加(表面张力增加)的程度。文中还对磷脂膜融合的分子机制进行了一些讨论。