Sisk R B, Huang C H
Department of Biochemistry, University of Virginia, Charlottesville 22908.
Biophys J. 1992 Mar;61(3):593-603. doi: 10.1016/S0006-3495(92)81864-7.
Recent studies of five different phosphatidylcholine/phosphatidylcholine (PC/PC) systems indicate that binary mixtures of phosphatidylcholines in which one component has a normalized chain length difference (delta C/CL) in the range of 0.09-0.40 and the other a delta C/CL in the range of 0.42-0.57 exhibit the phase behavior of a eutectic system. Here, delta C is the effective chain-length difference between the two acyl chains, and CL is the effective length of the longer of the two acyl chains for the same lipid molecule in the gel state. In each mixture, gel phase immiscibility occurs over a wide compositional range due to the difference in the gel phase acyl chain packing properties of each component. Although the mixtures differ in the location of their eutectic horizontal, with respect to temperature, all have a similar eutectic point that occurs at a composition of approximately 40 mol percent of the component with the delta C/CL value in the range of 0.42-0.57. Here, we extend these studies by systematically modifying the headgroup of C(17):C(17)PC and then analyzing the mixing behavior of the modified lipid with C(22):C(12)PC using DSC. Progressive demethylation of the C(17):C(17)PC headgroup leads to an increase in gel phase immiscibility and a decrease in the amount of C(22):C(12)PC that comprises the eutectic composition. The temperature defining the location of the eutectic horizontal, however, remains virtually unchanged in all three phase diagrams. Our results suggest that the eutectic composition is influenced by changes in gel phase acyl chain packing that are dependent on headgroup-headgroup interactions. In contrast, the eutectic nature of the phase diagram and the location of its solidus line are properties of acyl chain interactions that are independent of phospholipid headgroup-headgroup interactions.
最近对五种不同的磷脂酰胆碱/磷脂酰胆碱(PC/PC)体系的研究表明,其中一种组分的归一化链长差(δC/CL)在0.09 - 0.40范围内,另一种组分的δC/CL在0.42 - 0.57范围内的磷脂酰胆碱二元混合物表现出低共熔体系的相行为。在此,δC是两条酰基链之间的有效链长差,CL是同一脂质分子在凝胶态时两条酰基链中较长链的有效长度。在每种混合物中,由于各组分凝胶相酰基链堆积性质的差异,凝胶相不混溶性在很宽的组成范围内都会出现。尽管这些混合物的低共熔水平线位置随温度不同而有所差异,但所有混合物都有一个相似的低共熔点,该点出现在δC/CL值在0.42 - 0.57范围内的组分含量约为40摩尔百分比的组成处。在此,我们通过系统修饰C(17):C(17)PC的头基,然后使用差示扫描量热法(DSC)分析修饰后的脂质与C(22):C(12)PC的混合行为来扩展这些研究。C(17):C(17)PC头基的逐步去甲基化导致凝胶相不混溶性增加,且构成低共熔组成的C(22):C(12)PC的量减少。然而,在所有三个相图中,定义低共熔水平线位置的温度实际上保持不变。我们的结果表明,低共熔组成受依赖于头基 - 头基相互作用的凝胶相酰基链堆积变化的影响。相比之下,相图的低共熔性质及其固相线的位置是酰基链相互作用的特性,与磷脂头基 - 头基相互作用无关。