Tsamaloukas Alekos, Szadkowska Halina, Slotte Peter J, Heerklotz Heiko
Biozentrum of the University of Basel, Division of Biophysical Chemistry, Switzerland.
Biophys J. 2005 Aug;89(2):1109-19. doi: 10.1529/biophysj.105.061846. Epub 2005 May 27.
Interactions of cholesterol (cho) with different lipids are commonly believed to play a key role in the formation of functional domains in membranes. We introduce a novel approach to characterize cho-lipid interactions by isothermal titration calorimetry. Cho is solubilized in the aqueous phase by reversible complexation with methyl-beta-cyclodextrin (cyd). Uptake of cho into the membrane is measured upon a series of injections of lipid vesicles into a cyd/cho solution. As an independent assay, cho release from membranes is measured upon titrating lipid/cho mixed vesicles into a cyd solution. The most consistent fit to the data is obtained with a mole fraction (rather than mole ratio) partition coefficient and considering a cho/cyd stoichiometry of 1:2. The results are discussed in terms of contributions from 1), the transfer of cho from cyd into a hypothetical, ideally mixed membrane and 2), from nonideal interactions with POPC. The latter are exothermic but opposed by a strong loss in entropy, in agreement with cho-induced acyl chain ordering and membrane condensation. They are accompanied by a positive heat capacity change which cannot be interpreted in terms of the hydrophobic effect, suggesting that additive-induced chain ordering itself increases the heat capacity. The new assays have a great potential for a better understanding of sterol-lipid interactions and yield suggestions how to optimize cho extraction from membranes.
胆固醇(Cho)与不同脂质的相互作用通常被认为在膜功能域的形成中起关键作用。我们引入了一种通过等温滴定量热法来表征胆固醇 - 脂质相互作用的新方法。胆固醇通过与甲基 - β - 环糊精(cyd)可逆络合而溶解于水相中。在将一系列脂质囊泡注入cyd / Cho溶液时,测量胆固醇进入膜的摄取量。作为一种独立的测定方法,在将脂质/胆固醇混合囊泡滴定到cyd溶液中时,测量胆固醇从膜中的释放量。使用摩尔分数(而非摩尔比)分配系数并考虑胆固醇/环糊精化学计量比为1:2时,能得到与数据最一致的拟合。从以下两个方面讨论了结果:1)胆固醇从环糊精转移到假设的理想混合膜中,以及2)与1 - 棕榈酰 - 2 - 油酰 - 磷脂酰胆碱(POPC)的非理想相互作用。后者是放热的,但被熵的强烈损失所抵消,这与胆固醇诱导的酰基链有序化和膜凝聚一致。它们伴随着正的热容变化,这不能用疏水效应来解释,表明添加剂诱导的链有序化本身增加了热容。这些新的测定方法对于更好地理解甾醇 - 脂质相互作用具有很大潜力,并为如何优化从膜中提取胆固醇提供了建议。