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膜表面之间的离子特异性表面力。

Ion specific surface forces between membrane surfaces.

作者信息

Boström M, Deniz V, Ninham B W

机构信息

Department of Physics and Measurement Technology, Linköping University, SE-581 83 Linköping, Sweden.

出版信息

J Phys Chem B. 2006 May 18;110(19):9645-9. doi: 10.1021/jp0606560.

Abstract

Entities such as ion distributions and forces between lipid membranes depend on effects due to the intervening salt solution that have not been recognized previously. These specific ion or Hofmeister effects influence membrane fusion. A typical illustrative example is this: measurements of forces between double-chained cationic bilayers adsorbed onto molecularly smooth mica surfaces across different 0.6-2 mM salt solutions have revealed a large degree of ion specificity [Pashley et al. J. Phys. Chem. 1986, 90, 1637]. This has been interpreted in terms of very specific anion "binding" to the adsorbed bilayers, as it would too for micelles and other self-assembled systems. However, we show here that inclusion of nonelectrostatic (NES) or ionic dispersion potentials acting between ions and the two surfaces explains such "ion binding". The observed Hofmeister sequence for the calculated pressure without any direct ion binding is given correctly. This demonstrates the importance of a source of ion specificity that has been ignored. It is due to ionic physisorption caused by attractive NES ionic dispersion potentials. There appear to be some far reaching consequences for interpretations of membrane intermolecular interactions in salt solutions.

摘要

诸如离子分布和脂质膜之间的作用力等实体,取决于此前未被认识到的中间盐溶液所产生的效应。这些特定的离子效应或霍夫迈斯特效应会影响膜融合。一个典型的示例如下:在不同的0.6 - 2 mM盐溶液中,对吸附在分子光滑云母表面的双链阳离子双层膜之间的力进行测量,结果显示出很大程度的离子特异性[帕什利等人,《物理化学杂志》,1986年,第90卷,第1637页]。这被解释为非常特定的阴离子“结合”到吸附的双层膜上,对于胶束和其他自组装体系也是如此。然而,我们在此表明,离子与两个表面之间作用的非静电(NES)或离子分散势的纳入,能够解释这种“离子结合”。对于没有任何直接离子结合情况下计算出的压力,所观察到的霍夫迈斯特序列是正确给出的。这证明了一个被忽视的离子特异性来源的重要性。这是由有吸引力的NES离子分散势引起的离子物理吸附所致。对于盐溶液中膜分子间相互作用的解释,似乎存在一些深远的影响。

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