Lu Yangyi, Zhong Dongping
Department of Physics, Department of Chemistry and Biochemistry, Programs of Biophysics, Chemical Physics, and Biochemistry , The Ohio State University , Columbus , Ohio 43210 , United States.
Center for Ultrafast Science and Technology, School of Chemistry and Chemical Engineering, School of Physics and Astronomy , Shanghai Jiao Tong University , Shanghai 200240 , China.
J Phys Chem Lett. 2019 Feb 7;10(3):346-351. doi: 10.1021/acs.jpclett.8b03749. Epub 2019 Jan 10.
Short-range electron-transfer (ET) reactions in biological systems are usually ultrafast, having transfer rates comparable to or even faster than corresponding environmental fluctuations, and often display nonexponential behaviors. To understand these nonequilibrium ET dynamics, we carried out detailed theoretical analyses based on the Sumi-Marcus model. It is shown that the ET dynamics is largely determined by the relative time scales of the ET reaction and its surrounding motions. Significantly, different environmental fluctuations can produce a variety of apparent ET dynamics even with the same driving force, Δ G, and reorganization energy, λ. We applied our analyses to an ultrafast ET process in DNA repair by (6-4) photolyase and directly obtained the inner and outer reorganization energies (λ and λ) as well as the free energy Δ G of various mutants, providing mechanical insight into ultrafast short-range ET reactions in proteins.
生物系统中的短程电子转移(ET)反应通常极快,其转移速率与相应的环境涨落相当,甚至比环境涨落更快,并且常常表现出非指数行为。为了理解这些非平衡ET动力学,我们基于苏米-马库斯模型进行了详细的理论分析。结果表明,ET动力学在很大程度上由ET反应及其周围运动的相对时间尺度决定。值得注意的是,即使驱动力ΔG和重组能λ相同,不同的环境涨落也会产生各种明显的ET动力学。我们将分析应用于(6-4)光裂合酶修复DNA的超快ET过程,直接获得了各种突变体的内重组能和外重组能(λ和λ)以及自由能ΔG,为蛋白质中超快短程ET反应提供了力学见解。