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扩展的疏水和亲水表面附近的水的波动。

Fluctuations of water near extended hydrophobic and hydrophilic surfaces.

机构信息

Department of Chemistry, University of California, Berkeley, California 94720, USA.

出版信息

J Phys Chem B. 2010 Feb 4;114(4):1632-7. doi: 10.1021/jp909048f.

Abstract

We use molecular dynamics simulations of the SPC-E model of liquid water to derive probability distributions for water density fluctuations in probe volumes of different shapes and sizes, both in the bulk as well as near hydrophobic and hydrophilic surfaces. Our results are obtained with a biased sampling of coarse-grained densities that is easily combined with molecular dynamics integration algorithms. Our principal result is that the probability for density fluctuations of water near a hydrophobic surface, with or without surface water attractions, is akin to density fluctuations at the water-vapor interface. Specifically, the probability of density depletion near the surface is significantly larger than that in the bulk, and this enhanced probability is responsible for hydrophobic forces of assembly. In contrast, we find that the statistics of water density fluctuations near a model hydrophilic surface are similar to that in the bulk.

摘要

我们使用 SPC-E 模型的分子动力学模拟来推导不同形状和大小探针体积中液体水密度涨落的概率分布,包括在体相以及疏水和亲水表面附近。我们的结果是通过对粗粒密度进行有偏采样获得的,这种采样方法易于与分子动力学积分算法结合。我们的主要结果是,在有或没有表面水吸引力的情况下,水在疏水表面附近的密度涨落的概率类似于水蒸气界面处的密度涨落。具体来说,表面附近的密度亏缺的概率显著大于体相中的概率,这种增强的概率是导致疏水组装力的原因。相比之下,我们发现模型亲水表面附近水密度涨落的统计数据与体相相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8389/3173972/944177da79e0/nihms169706f1.jpg

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