A Configuration Interaction Picture for a Molecular Environment Using Localized Molecular Orbitals: The Excited States of Retinal Proteins
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- 作者：Jun-ya Hasegawa ; Kazuhiro J. Fujimoto ; Tsutomu Kawatsu
- 刊名：Journal of Chemical Theory and Computation
- 出版年：2012
- 出版时间：November 13, 2012
- 年：2012
- 卷：8
- 期：11
- 页码：4452-4461
- 全文大小：616K
- 年卷期：v.8,no.11(November 13, 2012)
- ISSN：1549-9626
文摘
Electronic excitations of chromophores in proteins and solutions are associated with the electronic response of the molecular environment. The underlying interactions are important origins of solvatochromism. We performed large-scale configuration interaction singles (CIS) calculations (up to 1000 atoms) for retinal chromophores in proteins and methanol solution, in which one-electron processes (polarization and charge-transfer effects of the environment) are included. The present approach also improved the electrostatic potential, as compared to that described by a molecular mechanics (MM) force field. The CIS results were combined with the symmetry adapted cluster (SAC)-CI result using our own N-layer integrated molecular orbital molecular mechanics (ONIOM) method. As compared to the MM description, the CIS reduces the calculated excitation energy by 0.1鈥?.3 eV and also improves the relative excitation energies among retinal proteins. We applied our localized molecular orbital (LMO) transformation scheme to analyze the CI wave functions. The result clarified the contributions of the amino acids. In bacteriorhodopsin, Tyr185 contributes intermolecular CT excitations. The radial distribution of amino acids鈥?contributions to the CI wave function was also analyzed. The results of the analysis are useful not only for understanding the molecular interactions and the role of amino acids in color tuning, but also for providing insight into the structure of the excited-state wave function for the molecular environment. An excitation-energy decomposition analysis also supported the results of the excited-state wave functions.