Laptenok S P, Conyard J, Page P C Bulman, Chan Y, You M, Jaffrey S R, Meech S R
School of Chemistry, University of East Anglia, Norwich NR4 7TJ, UK.
Department of Pharmacology Weill Medical College of Cornell University 1300 York Avenue, Box 70 New York, NY 10065, USA.
Chem Sci. 2016;7(9):5747-5752. doi: 10.1039/C6SC02031C. Epub 2016 Jun 6.
The photophysics of the chromophore of the green fluorescent protein in (avGFP) are dominated by an excited state proton transfer reaction. In contrast the photophysics of the same chromophore in solution are dominated by radiationless decay, and photoacid behaviour is not observed. Here we show that modification of the p of the chromophore by fluorination leads to an excited state proton transfer on an extremely fast (50 fs) time scale. Such a fast rate suggests a barrierless proton transfer and the existence of a pre-formed acceptor site in the aqueous solution, which is supported by solvent and deuterium isotope effects. In addition, at lower pH, photochemical formation of the elusive zwitterion of the GFP chromophore is observed by means of an equally fast excited state proton transfer from the cation. The significance of these results for understanding and modifying the properties of fluorescent proteins are discussed.
绿色荧光蛋白(avGFP)发色团的光物理过程主要由激发态质子转移反应主导。相比之下,同一发色团在溶液中的光物理过程则主要由无辐射衰变主导,并且未观察到光酸行为。在此我们表明,通过氟化对发色团的p进行修饰会导致在极快(50飞秒)的时间尺度上发生激发态质子转移。如此快的速率表明质子转移无势垒,且在水溶液中存在预先形成的受体位点,这得到了溶剂和氘同位素效应的支持。此外,在较低pH值下,通过同样快速的从阳离子进行的激发态质子转移,观察到了GFP发色团难以捉摸的两性离子的光化学形成。讨论了这些结果对于理解和修饰荧光蛋白性质的意义。