Lafleur M, Bloom M, Eikenberry E F, Gruner S M, Han Y, Cullis P R
Département de chimie, Université de Montréal, Québec, Canada.
Biophys J. 1996 Jun;70(6):2747-57. doi: 10.1016/S0006-3495(96)79844-2.
The 1-palmitoyl-2-oleoyl-phosphatidylethanolamine: 1-palmitoyl-2-oleoyl-phosphatidylcholine (POPE:POPC) system has been investigated by measuring, in the inverted hexagonal (HII) phase, the intercylinder spacings (using x-ray diffraction) and orientational order of the acyl chains (using 2H nuclear magnetic resonance). The presence of 20 wt% dodecane leads to the formation of a HII phase for the composition range from 0 to 39 mol% of POPC in POPE, as ascertained by x-ray diffraction and 2H nuclear magnetic resonance. The addition of the alkane induces a small decrease in chain order, consistent with less stretched chains. An increase in temperature or in POPE proportion leads to a reduction in the intercylinder spacing, primarily due to a decrease in the water core radius. A temperature increase also leads to a reduction in the orientational order of the lipid acyl chains, whereas the POPE proportion has little effect on chain order. A correlation is proposed to relate the radius of curvature of the cylinders in the inverted hexagonal phase to the chain order of the lipids adopting the HII phase. A simple geometrical model is proposed, taking into account the area occupied by the polar headgroup at the interface and the orientational order of the acyl chains reflecting the contribution of the apolar core. From these parameters, intercylinder spacings are calculated that agree well with the values determined experimentally by x-ray diffraction, for the variations of both temperature and POPE:POPC proportion. This model suggests that temperature increases the curvature of lipid layers, mainly by increasing the area subtended by the hydrophobic core through chain conformation disorder, whereas POPC content affects primarily the headgroup interface contribution. The frustration of lipid layer curvature is also shown to be reflected in the acyl chain order measured in the L alpha phase, in the absence of dodecane; for a given temperature, increased order is observed when the curling tendencies of the lipid plane are more pronounced.
通过在反相六角(HII)相中测量柱间间距(使用X射线衍射)和酰基链的取向有序性(使用2H核磁共振),对1-棕榈酰基-2-油酰基磷脂酰乙醇胺:1-棕榈酰基-2-油酰基磷脂酰胆碱(POPE:POPC)体系进行了研究。通过X射线衍射和2H核磁共振确定,20 wt%十二烷的存在导致在POPE中POPC含量为0至39 mol%的组成范围内形成HII相。烷烃的加入导致链有序性略有降低,这与链伸展程度降低一致。温度升高或POPE比例增加会导致柱间间距减小,这主要是由于水核半径减小。温度升高还会导致脂质酰基链的取向有序性降低,而POPE比例对链有序性影响不大。提出了一种相关性,将反相六角相中圆柱的曲率半径与采用HII相的脂质的链有序性联系起来。提出了一个简单的几何模型,该模型考虑了界面处极性头基所占的面积以及反映非极性核心贡献的酰基链的取向有序性。根据这些参数计算出的柱间间距与通过X射线衍射实验测定的值在温度和POPE:POPC比例变化时都非常吻合。该模型表明,温度主要通过增加疏水核心所占据的面积(通过链构象无序)来增加脂质层的曲率,而POPC含量主要影响头基界面的贡献。在没有十二烷的情况下,脂质层曲率的受挫也反映在Lα相中测量的酰基链有序性上;在给定温度下,当脂质平面的卷曲趋势更明显时,会观察到有序性增加。