Mukhopadhyay Abhishek, Tolokh Igor S, Onufriev Alexey V
†Department of Physics and ‡Department of Computer Science, Virginia Tech, Blacksburg, Virginia 24061, United States.
J Phys Chem B. 2015 May 21;119(20):6092-100. doi: 10.1021/acs.jpcb.5b00602. Epub 2015 May 7.
Charge hydration asymmetry (CHA)-a characteristic dependence of hydration free energy on the sign of the solute charge-quantifies the asymmetric response of water to electric field at microscopic level. Accurate estimates of CHA are critical for understanding hydration effects ubiquitous in chemistry and biology. However, measuring hydration energies of charged species is fraught with significant difficulties, which lead to unacceptably large (up to 300%) variation in the available estimates of the CHA effect. We circumvent these difficulties by developing a framework which allows us to extract and accurately estimate the intrinsic propensity of water to exhibit CHA from accurate experimental hydration free energies of neutral polar molecules. Specifically, from a set of 504 small molecules we identify two pairs that are analogous, with respect to CHA, to the K(+) /F(-) pair-a classical probe for the effect. We use these "CHA-conjugate" molecule pairs to quantify the intrinsic charge-asymmetric response of water to the microscopic charge perturbations: the asymmetry of the response is strong, ∼50% of the average hydration free energy of these molecules. The ability of widely used classical water models to predict hydration energies of small molecules correlates with their ability to predict CHA.
电荷水合不对称性(CHA)——水合自由能对溶质电荷符号的特征依赖性——在微观层面量化了水对电场的不对称响应。准确估计CHA对于理解化学和生物学中普遍存在的水合效应至关重要。然而,测量带电物种的水合能存在重大困难,这导致CHA效应的现有估计值出现高达300%的不可接受的大变化。我们通过开发一个框架来规避这些困难,该框架使我们能够从精确的中性极性分子实验水合自由能中提取并准确估计水表现出CHA的内在倾向。具体而言,从一组504个小分子中,我们确定了两对在CHA方面类似于K(+) /F(-)对(该效应的经典探针)的分子对。我们使用这些“CHA共轭”分子对来量化水对微观电荷扰动的内在电荷不对称响应:响应的不对称性很强,约为这些分子平均水合自由能的50%。广泛使用的经典水模型预测小分子水合能的能力与其预测CHA的能力相关。