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首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Ultrafast Excited and Ground-State Dynamics of the Green Fluorescent Protein Chromophore in Solution
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Ultrafast Excited and Ground-State Dynamics of the Green Fluorescent Protein Chromophore in Solution

机译:溶液中绿色荧光蛋白发色团的超快激发态和基态动力学

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摘要

Ultrafast dispersed pump-dump-probe spectroscopy was applied to HBDI (4'-hydroxybenzylidene-2,3-dimethyl-imidazolinone), a model green fluorescent protein (GFP) chromophore in solution with different protonation states. The measured three-dimensional data was analyzed using a global analysis method that enables the spectral and temporal characterization of overlapping photoinduced transient states. A unified phenomenological model is presented to describe the observed data. Two excitation pathways are identified: a 1-photon excited-state twisting and a 2-photon ionization process. The ionization pathway results in the generation of solvated electrons and HBDI radicals. The twisting dynamics was resolved on both electronic states with slower twisting on the ground state than the excited state. This is ascribed to the multidimensional hula-twist mechanism. A weak viscosity dependence was observed when the aqueous solution data were contrasted with the signals collected in a 66% glycerol/water solution.
机译:将超快分散泵浦-转储-探针光谱法应用于HBDI(4'-羟基亚苄基-2,3-二甲基-咪唑啉酮),这是一种具有不同质子化状态的模型绿色荧光蛋白(GFP)发色团。使用全局分析方法对测量的三维数据进行了分析,该方法能够对重叠的光诱导瞬态进行光谱和时间表征。提出了统一的现象学模型来描述观察到的数据。确定了两个激发途径:1-光子激发态扭曲和2-光子电离过程。电离途径导致溶剂化电子和HBDI自由基的产生。在两种电子状态下都解决了扭转动力学问题,在基态上的扭转比在激发态下慢。这归因于多维呼啦扭曲机制。当水溶液数据与在66%甘油/水溶液中收集的信号进行对比时,观察到了较弱的粘度依赖性。

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