El Mashak E M, Lakhdar-Ghazal F, Tocanne J F
Biochim Biophys Acta. 1982 Jun 14;688(2):465-74. doi: 10.1016/0005-2736(82)90358-3.
The mixing of various molecular species of phosphatidylglycerol and phosphatidylcholine differing in their acyl chain lengths has been studied both in monolayers (pi, delta V), and in water dispersions (fluorescence polarization) with varying pH and ionic strength of the aqueous phase and in the presence of the divalent cations Mg2+ and Ca2+. In dilauroylphosphatidylglycerol/dipalmitoylphosphatidylcholine mixtures, both in monolayers and in water dispersions, no phase separation was detected at pH 2.9 where phosphatidylglycerol was protonated. With dipalmitoylphosphatidylglycerol/dipalmitoylphosphatidylcholine mixtures, in monolayers and at the same pH, no phase separation was detected for surface pressures below pi = 40 mN.m-1. In monolayers, and under ionic conditions such that phosphatidylglycerol was ionized (pH 5.6, 10 mM NaCl) miscibility was observed with dilauroylphosphatidylglycerol and dipalmitoylphosphatidylcholine and also with dipalmitoylphosphatidylglycerol and dilauroylphosphatidylcholine. Varying the ionic strength did not alter the miscibility of these lipids. The divalent cations Mg2+ and Ca2+ did not modify that of dilauroylphosphatidylglycerol with dilauroylphosphatidylcholine or with dipalmitoylphosphatidylcholine. Both in monolayers and in water dispersions, dipalmitoylphosphatidylglycerol and dilauroylphosphatidylcholine appeared to be at least partly miscible, in the presence of magnesium. Only in the presence of calcium and at high surface pressure might the monolayer data account for phase separation between these two lipids. The data presented demonstrate the existence of strong cohesive forces between phosphatidylcholine and phosphatidylglycerol with a marked influence of the former on the physical state of the latter. From an analysis of the delta V data, it is suggested that intrafacial hydrogen bonds may play a significant role in stabilizing phosphatidylcholine/phosphatidylglycerol mixtures.
研究了不同酰基链长度的磷脂酰甘油和磷脂酰胆碱的各种分子种类在单层膜(π,ΔV)以及水相中pH值和离子强度不同且存在二价阳离子Mg2+和Ca2+的水乳液(荧光偏振)中的混合情况。在二月桂酰磷脂酰甘油/二棕榈酰磷脂酰胆碱混合物中,无论是在单层膜还是水乳液中,在pH 2.9(此时磷脂酰甘油质子化)时均未检测到相分离。对于二棕榈酰磷脂酰甘油/二棕榈酰磷脂酰胆碱混合物,在单层膜且相同pH值下,当表面压力低于π = 40 mN·m-1时未检测到相分离。在单层膜中,在使磷脂酰甘油离子化的离子条件下(pH 5.6,10 mM NaCl),观察到二月桂酰磷脂酰甘油与二棕榈酰磷脂酰胆碱以及二棕榈酰磷脂酰甘油与二月桂酰磷脂酰胆碱可混溶。改变离子强度并未改变这些脂质的混溶性。二价阳离子Mg2+和Ca2+并未改变二月桂酰磷脂酰甘油与二月桂酰磷脂酰胆碱或与二棕榈酰磷脂酰胆碱的混溶性。无论是在单层膜还是水乳液中,在镁存在的情况下,二棕榈酰磷脂酰甘油和二月桂酰磷脂酰胆碱似乎至少部分可混溶。仅在钙存在且表面压力较高时,单层膜数据才可能解释这两种脂质之间的相分离。所呈现的数据表明磷脂酰胆碱和磷脂酰甘油之间存在强大的内聚作用力,前者对后者的物理状态有显著影响。通过对ΔV数据的分析,表明界面内氢键可能在稳定磷脂酰胆碱/磷脂酰甘油混合物中起重要作用。