Berde C B, Andersen H C, Hudson B S
Biochemistry. 1980 Sep 2;19(18):4279-93. doi: 10.1021/bi00559a021.
We have developed statistical mechanical descriptions of the effects of head-group structure and acyl chain unsaturation on the chain melting phase transition of aqueous dispersions of bilayers containing glycerophosphocholines and glycerophosphoethanolamines. The theoretical framework is an extension of the model of Jacobs et al. [Jacobs, R. E., Hudson, B. S., & Andersen, H. C. (1975) Proc. Natl. Acad. Sci. U.S.A. 72, 3993]. There are several systematic trends in the experimental transition data for various types of phospholipids. Assumptions about the physical origins of these trends were incorporated into statistical mechanical models, which were used to calculate transition temperatures and enthalpies. The extent to which the calculated results of a model reproduce the experimental trends is taken as a measure of the validity of the assumptions on which the model is based. We found that the gross differences among the transition temperatures of phospholipids with two saturated chains, two trans-unsaturated chains, two cis-unsaturated chains, and one cis-unsaturated and one saturated chain can all be explained in terms of the effect of the double bonds on molecular shape and the subsequent effect of shape on the ability of molecules to pack together into a low-energy state at high density. The dependence of transition temperature on the location of the double bond in cis-unsaturated molecules can be understood on the same basis. The differences between the transition temperatures of glycerophosphocholines and glycerophosphoethanolamines with the same hydrocarbon chains can be explained in terms of a larger intermolecular attraction (or smaller repulsion) for the latter than for the former. These differences depend on the presence or absence of unsaturation in the hydrocarbon chains in a way that is consistent with the postulate that hydrogen bonding between glycerophosphoethanolamines is responsible for the differences.
我们已经建立了统计力学描述,用于研究头基结构和酰基链不饱和度对含有甘油磷酸胆碱和甘油磷酸乙醇胺的双层水相分散体链熔化相变的影响。该理论框架是对雅各布斯等人模型的扩展[雅各布斯,R.E.,哈德森,B.S.,& 安德森,H.C.(1975年)《美国国家科学院院刊》72,3993]。各种类型磷脂的实验转变数据存在若干系统趋势。关于这些趋势物理起源的假设被纳入统计力学模型,用于计算转变温度和焓。模型计算结果再现实验趋势的程度被用作衡量模型所基于假设有效性的指标。我们发现,具有两条饱和链、两条反式不饱和链、两条顺式不饱和链以及一条顺式不饱和链和一条饱和链的磷脂转变温度之间的总体差异,都可以根据双键对分子形状的影响以及形状对分子在高密度下聚集形成低能态能力的后续影响来解释。顺式不饱和分子中转变温度对双键位置的依赖性也可以基于相同的基础来理解。具有相同烃链的甘油磷酸胆碱和甘油磷酸乙醇胺转变温度之间的差异,可以根据后者比前者具有更大的分子间吸引力(或更小的排斥力)来解释。这些差异取决于烃链中不饱和键的有无,其方式与甘油磷酸乙醇胺之间的氢键作用导致差异这一假设相一致。