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本文引用的文献

1
PIP2 signaling in lipid domains: a critical re-evaluation.脂类结构域中的磷脂酰肌醇-4,5-二磷酸信号传导:一项关键的重新评估
EMBO J. 2005 May 4;24(9):1664-73. doi: 10.1038/sj.emboj.7600655. Epub 2005 Apr 21.
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Model systems, lipid rafts, and cell membranes.模型系统、脂筏与细胞膜。
Annu Rev Biophys Biomol Struct. 2004;33:269-95. doi: 10.1146/annurev.biophys.32.110601.141803.
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Liquid domains in vesicles investigated by NMR and fluorescence microscopy.通过核磁共振和荧光显微镜对囊泡中的液体区域进行研究。
Biophys J. 2004 May;86(5):2910-22. doi: 10.1016/S0006-3495(04)74342-8.
4
Calorimetric measurement of phospholipid interaction with methyl-beta-cyclodextrin.磷脂与甲基-β-环糊精相互作用的量热法测量
Biochemistry. 2004 Mar 2;43(8):2251-61. doi: 10.1021/bi0358869.
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Lipid rafts: elusive or illusive?脂筏:难以捉摸还是虚幻不实?
Cell. 2003 Nov 14;115(4):377-88. doi: 10.1016/s0092-8674(03)00882-1.
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Sphingomyelin/phosphatidylcholine/cholesterol phase diagram: boundaries and composition of lipid rafts.鞘磷脂/磷脂酰胆碱/胆固醇相图:脂筏的边界与组成
Biophys J. 2003 Oct;85(4):2406-16. doi: 10.1016/S0006-3495(03)74664-5.
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Time-resolved fluorescence and fourier transform infrared spectroscopic investigations of lateral packing defects and superlattice domains in compositionally uniform cholesterol/phosphatidylcholine bilayers.对组成均匀的胆固醇/磷脂酰胆碱双层膜中侧向堆积缺陷和超晶格域的时间分辨荧光和傅里叶变换红外光谱研究。
Biophys J. 2003 Jun;84(6):3777-91. doi: 10.1016/S0006-3495(03)75106-6.
8
A calorimetric study of binary mixtures of dihydrosphingomyelin and sterols, sphingomyelin, or phosphatidylcholine.二氢鞘磷脂与固醇、鞘磷脂或磷脂酰胆碱二元混合物的量热研究。
Biophys J. 2003 May;84(5):3138-46. doi: 10.1016/s0006-3495(03)70038-1.
9
Role of cholesterol in lipid raft formation: lessons from lipid model systems.胆固醇在脂筏形成中的作用:来自脂质模型系统的经验教训。
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The state of lipid rafts: from model membranes to cells.脂筏的状态:从模型膜到细胞
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通过量热法表征胆固醇与脂质膜和环糊精的相互作用。

Interactions of cholesterol with lipid membranes and cyclodextrin characterized by calorimetry.

作者信息

Tsamaloukas Alekos, Szadkowska Halina, Slotte Peter J, Heerklotz Heiko

机构信息

Biozentrum of the University of Basel, Division of Biophysical Chemistry, Switzerland.

出版信息

Biophys J. 2005 Aug;89(2):1109-19. doi: 10.1529/biophysj.105.061846. Epub 2005 May 27.

DOI:10.1529/biophysj.105.061846
PMID:15923231
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1366596/
Abstract

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.

摘要

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。