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疏水离子跨脂质囊泡膜非稳态扩散的理论描述,包括水相中离子-离子相互作用的影响。

A theoretical description of non-steady-state diffusion of hydrophobic ions across lipid vesicle membranes including effects of ion-ion interactions in the aqueous phase.

作者信息

Clarke R J

机构信息

Fritz-Haber-Institut der Max-Planck-Gesellschaft, Berlin, Germany.

出版信息

Biophys Chem. 1993 Apr;46(2):131-43. doi: 10.1016/0301-4622(93)85020-i.

Abstract

A theoretical model of hydrophobic ion diffusion across vesicular membranes is presented, which is based upon activated rate theory. The model is applicable to the sudden addition of hydrophobic ions to a vesicle suspension, for example in a stopped-flow experiment. The time course of diffusion is calculated by numerical integration of differential rate equations for the ion concentrations and electrical potential differences across the membrane. The model utilizes the three-capacitor model of the membrane and an extended Debye-Hückel theory, taking into account non-neutrality on each side of the membrane. At low ionic strengths good agreement is found between the infinite time diffusion potential and the equilibrium Nernst potential. At large excess of inert electrolyte discrepancies are found, but under such conditions the membrane potential is negligible due to screening.

摘要

提出了一种基于活化速率理论的疏水离子跨囊泡膜扩散的理论模型。该模型适用于例如在停流实验中向囊泡悬浮液中突然添加疏水离子的情况。扩散的时间进程通过对膜两侧离子浓度和电势差的微分速率方程进行数值积分来计算。该模型利用了膜的三电容模型和扩展的德拜 - 休克尔理论,考虑了膜两侧的非电中性。在低离子强度下,发现无限时间扩散电位与平衡能斯特电位之间有良好的一致性。在惰性电解质大量过量的情况下,发现存在差异,但在这种条件下,由于屏蔽作用,膜电位可忽略不计。

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