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Modulation of electron transfer kinetics by protein conformational fluctuations during early-stage photosynthesis

机译:早期光合作用中蛋白质构象波动对电子转移动力学的调节

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The kinetics of electron transfer during the early stages of the photosynthetic reaction cycle has recently been shown in transient absorption experiments carried out by Wang et al. [Science 316, 747 (2007)] to be strongly influenced by fluctuations in the conformation of the surrounding protein. A model of electron transfer rates in polar solvents developed by Sumi and Marcus using a reaction-diffusion formalism [J. Chem. Phys. 84, 4894 (1986)] was found to be successful in fitting the experimental absorption curves over a roughly 200 ps time interval. The fits were achieved using an empirically determined time-dependent function that described protein conformational relaxation. In the present paper, a microscopic model of this function is suggested, and it is shown that the function can be identified with the dynamic autocorrelation function of intersegment distance fluctuations that occur in a harmonic potential of mean force under the action of fractional Gaussian noise.
机译:Wang等人进行的瞬态吸收实验最近显示了光合作用循环早期阶段电子转移的动力学。 [Science 316,747(2007)]受周围蛋白质构象波动的强烈影响。 Sumi和Marcus利用反应扩散形式学建立了极性溶剂中电子转移速率的模型[J.化学物理84,4894(1986)]发现在大约200 ps的时间间隔内成功拟合了实验吸收曲线。使用描述蛋白质构象松弛的经验确定的时间依赖性函数来实现拟合。在本文中,提出了该函数的微观模型,并且表明该函数可以通过段间距离波动的动态自相关函数来识别,该段间距离波动是在分数高斯噪声的作用下,平均力的谐波势中发生的。

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