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巨泡的动力学弛豫验证了二元脂质混合物中的扩散软化。

Kinetic relaxation of giant vesicles validates diffusional softening in a binary lipid mixture.

机构信息

Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, 20892 Maryland, USA.

Max Planck Institute of Colloids and Interfaces, 14476 Potsdam, Germany.

出版信息

Phys Rev E. 2023 May;107(5-1):054403. doi: 10.1103/PhysRevE.107.054403.

Abstract

The stiffness of biological membranes determines the work required by cellular machinery to form and dismantle vesicles and other lipidic shapes. Model membrane stiffness can be determined from the equilibrium distribution of giant unilamellar vesicle surface undulations observable by phase contrast microscopy. With two or more components, lateral fluctuations of composition will couple to surface undulations depending on the curvature sensitivity of the constituent lipids. The result is a broader distribution of undulations whose complete relaxation is partially determined by lipid diffusion. In this work, kinetic analysis of the undulations of giant unilamellar vesicles made of phosphatidylcholine-phosphatidylethanolamine mixtures validates the molecular mechanism by which the membrane is made 25% softer than a single-component one. The mechanism is relevant to biological membranes, which have diverse and curvature-sensitive lipids.

摘要

生物膜的刚性决定了细胞机制形成和拆卸囊泡和其他脂质形状所需的功。模型膜的刚性可以通过相差显微镜观察到的巨大单层囊泡表面起伏的平衡分布来确定。对于两个或更多的成分,组成的横向波动将根据组成脂质的曲率敏感性与表面起伏耦合。结果是一个更广泛的波动分布,其完全松弛部分由脂质扩散决定。在这项工作中,对由磷脂酰胆碱-磷脂酰乙醇胺混合物制成的巨大单层囊泡的波动的动力学分析验证了使膜比单一组分软 25%的分子机制。该机制与具有多样化和曲率敏感脂质的生物膜有关。

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