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Ion specific effects: decoupling ion-ion and ion-water interactions

机译:离子特有的作用:分离离子与离子与水的相互作用

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摘要

Ion-specific effects in aqueous solution, known as the Hofmeister effect is prevalent in diverse systems ranging from pure ionic to complex protein solutions. The objective of this paper is to explicitly demonstrate how complex ion-ion and ion-water interactions manifest themselves in the Hofmeister effects, based on a series of recent experimental observation. These effects are not considered in the classical description of ion effects, such as the Deryaguin-Landau-Verwey-Overbeek (DLVO) theory that, likely for that reason, fail to describe the origin of the phenomenological Hofmeister effect. However, given that models considering the basic forces of electrostatic and van der Waals interactions can offer rationalization for the core experimental observations, a universal interaction model stands a chance to be developed. In this perspective, we separately derive the contribution from ion-ion electrostatic interaction and ion-water interaction from second harmonic generation (SHG) data at the air-ion solution interface, which yields an estimate of ion-water interactions in solution. Hofmeister ion effects observed on biological solutes in solution should be similarly influenced by contributions from ion-ion and ion-water interactions, where the same ion-water interaction parameters derived from SHG data at the air-ion solution interface could be applicable. A key experimental data set available from solution systems to probe ion-water interaction is the modulation of water diffusion dynamics near ions in bulk ion solution, as well as near biological liposome surfaces. It is obtained from Overhauser dynamic nuclear polarization (ODNP), a nuclear magnetic resonance (NMR) relaxometry technique. The surface water diffusivity is influenced by the contribution from ion-water interactions, both from localized surface charges and adsorbed ions, although the relative contribution of the former is larger on liposome surfaces. In this perspective, ion-water interaction energy values derived from experimental data for various ions are compared with theoretical values in the literature. Ultimately, quantifying ion-induced changes in surface energy for the purpose of developing valid theoretical models for ion-water interaction, will be critical to rationalizing the Hofmeister effect.
机译:水溶液中的离子特异性效应(称为Hofmeister效应)在从纯离子溶液到复杂蛋白质溶液的各种系统中都很普遍。本文的目的是根据一系列最近的实验观察结果,明确证明复杂的离子-离子和离子-水的相互作用如何在霍夫迈斯特效应中表现出来。在离子效应的经典描述中没有考虑这些效应,例如Deryaguin-Landau-Verwey-Overbeek(DLVO)理论,可能由于这个原因而无法描述现象学霍夫迈斯特效应的起源。但是,考虑到静电和范德华相互作用的基本力的模型可以为核心实验观察提供合理化,通用的相互作用模型有机会发展。从这个角度出发,我们分别从空气离子溶液界面的二次谐波生成(SHG)数据中得出离子-离子静电相互作用和离子-水相互作用的贡献,从而得出溶液中离子-水相互作用的估计值。溶液中生物溶质上观察到的霍夫迈斯特离子效应也应受到离子-离子和离子-水相互作用的贡献的类似影响,在空气-离子溶液界面处从SHG数据推导出的相同的离子-水相互作用参数也适用。溶液系统可用于探测离子与水相互作用的关键实验数据集是水在大体积离子溶液中离子附近以及生物脂质体表面附近的水扩散动力学的调节。它是通过Overhauser动态核极化(ODNP),核磁共振(NMR)弛豫技术获得的。表面水的扩散性受局部表面电荷和吸附离子的离子水相互作用的影响,尽管前者在脂质体表面的相对贡献较大。从这个角度来看,从各种离子的实验数据中得出的离子-水相互作用能值与文献中的理论值进行了比较。最终,为了开发有效的离子-水相互作用理论模型,量化离子诱导的表面能变化对于合理化霍夫迈斯特效应至关重要。

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