Ricardi Niccolò, González-Espinoza Cristina E, Adam Suliman, Church Jonathan R, Schapiro Igor, Wesołowski Tomasz Adam
Department of Physical Chemistry, University of Geneva, 1205 Geneva, Switzerland.
Fritz Haber Center for Molecular Dynamics, Hebrew University of Jerusalem Israel, 91904 Jerusalem, Israel.
J Chem Theory Comput. 2023 Aug 8;19(15):5289-5302. doi: 10.1021/acs.jctc.3c00285. Epub 2023 Jul 13.
Many simulation methods concerning solvated molecules are based on the assumption that the solvated species and the solvent can be characterized by some representative structures of the solute and some embedding potential corresponding to this structure. While the averaging of the solvent configurations to obtain an embedding potential has been studied in great detail, this hinges on a single solute structure representation. This assumption is re-examined and generalized for conformationally flexible solutes and tested on 4 nonrigid systems. In this generalized approach, the solute is characterized by a set of representative structures and the corresponding embedding potentials. The representative structures are identified by means of subdividing the statistical ensemble, which in this work is generated by a constant-temperature molecular dynamics simulation. The embedding potential defined in the Frozen-Density Embedding Theory is used to characterize the average effect of the solvent in each subensemble. The numerical examples concern the vertical excitation energies of protonated retinal Schiff bases in protein environments. It is comprehensively shown that subensemble averaging leads to huge computational savings compared with explicit averaging of the excitation energies in the whole ensemble while introducing only minor errors in the case of the systems examined.
溶剂化物种和溶剂可以通过溶质的一些代表性结构以及与该结构对应的某种嵌入势来表征。虽然为了获得嵌入势而对溶剂构型进行平均化处理已经得到了深入研究,但这依赖于单一的溶质结构表示。对于构象灵活的溶质,重新审视并推广了这一假设,并在4个非刚性体系上进行了测试。在这种广义方法中,溶质由一组代表性结构和相应的嵌入势来表征。通过对统计系综进行细分来确定代表性结构,在这项工作中,统计系综是由恒温分子动力学模拟生成的。在冻结密度嵌入理论中定义的嵌入势用于表征每个子系综中溶剂的平均效应。数值示例涉及蛋白质环境中质子化视黄醛席夫碱的垂直激发能。结果全面表明,与在整个系综中对激发能进行显式平均相比,子系综平均化在计算上能大幅节省,同时在所研究的体系中仅引入微小误差。