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Single Lipid Extraction: The Anchoring Strength of Cholesterol in Liquid-Ordered and Liquid-Disordered Phases

机译:单脂质提取:胆固醇在有序和无序液相中的锚固强度。

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摘要

Cholesterol is important for the formation of microdomains in supported lipid bilayers and is enriched in the liquid-ordered phase. To understand the interactions leading to this enrichment, we developed an AFM-based single-lipid-extraction (SLX) approach that enables us to determine the anchoring strength of cholesterol in the two phases of a phase-separated lipid membrane. As expected, the forces necessary for extracting a single cholesterol molecule from liquid-ordered phases are significantly higher than for extracting it from the liquid-disordered phases. Interestingly, application of the Bell model shows two energy barriers that correlate with the head and full length of the cholesterol molecule. The resulting lifetimes for complete extraction are 90 s and 11 s in the liquid-ordered and liquid-disordered phases, respectively. Molecular dynamics simulations of the very same experiment show similar force profiles and indicate that the stabilization of cholesterol in the liquid-ordered phase is mainly due to nonpolar contacts.
机译:胆固醇对于在支持的脂质双层中形成微区很重要,并且富含液相。为了了解导致这种富集的相互作用,我们开发了一种基于AFM的单脂质提取(SLX)方法,该方法使我们能够确定相分离脂质膜两相中胆固醇的锚固强度。如所期望的,从液相有序相中提取单个胆固醇分子所需的力显着高于从液相有序相中提取单一胆固醇分子的力。有趣的是,Bell模型的应用显示出与胆固醇分子的头部和全长相关的两个能垒。完全萃取的最终寿命在液相有序相和液相无序相中分别为90 s和11 s。完全相同的实验的分子动力学模拟显示出相似的作用力曲线,并表明在液相有序相中胆固醇的稳定化主要归因于非极性接触。

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