Dipartimento di Scienze Chimiche, Università di Napoli 'Federico II', Complesso Universitario di M. S. Angelo, via Cintia, I-80126 Napoli, Italy.
Phys Chem Chem Phys. 2013 Dec 21;15(47):20536-44. doi: 10.1039/c3cp52820k. Epub 2013 Nov 1.
In spite of the large number of experimental and theoretical studies, the optical absorption trend of the green fluorescent protein (GFP) chromophore in several environments has not been fully understood. We calculated at the same level of time dependent density functional theory the vertical excitation energy of the anionic GFP chromophore in the protein and in ethanol, dioxane, methanol and water solutions. As result, we reproduced for the first time the experimental trend of the absorption peaks with 0.015 eV as the standard deviation of the accuracy. This systematic error allowed us to analyze with confidence the relative weight of several solvation effects on the vertical excitation energy. Experimental trends not correlated with the solvent polarity were therefore explained with a fine balance of different steric and electronic effects on the photophysics of the chromophore. As an indirect and remarkable result, the present analysis confirms that the optical absorption of the chromophore in the gas phase is close to the value of 2.84 eV extrapolated by Dong et al. (J. Am. Chem. Soc., 2006, 128, 12038), and, as a consequence, that the protein environment induces a red shift of 0.23 eV.
尽管进行了大量的实验和理论研究,但绿色荧光蛋白(GFP)发色团在几种环境中的光学吸收趋势仍未被完全理解。我们在相同的含时密度泛函理论水平上计算了蛋白质中和乙醇、二氧杂环己烷、甲醇和水溶液中阴离子 GFP 发色团的垂直激发能。因此,我们首次以 0.015 eV 的标准偏差重现了实验趋势。这种系统误差使我们能够有信心地分析几个溶剂化效应对垂直激发能的相对权重。因此,与溶剂极性不相关的实验趋势可以通过对发色团光物理的不同空间和电子效应的精细平衡来解释。作为一个间接而显著的结果,目前的分析证实,发色团在气相中的光吸收值与 Dong 等人(J. Am. Chem. Soc.,2006,128,12038)外推的 2.84 eV 值接近,因此,蛋白质环境诱导了 0.23 eV 的红移。