天青
电子转移
化学物理
肌红蛋白
化学
氧化还原
兰姆达
金属蛋白
细胞色素c
结晶学
计算化学
光化学
金属
物理
生物化学
无机化学
线粒体
量子力学
有机化学
作者
Harry B. Gray,Jay R. Winkler
标识
DOI:10.1146/annurev.bi.65.070196.002541
摘要
Electron-transfer (ET) reactions are key steps in a diverse array of biological transformations ranging from photosynthesis to aerobic respiration. A powerful theoretical formalism has been developed that describes ET rates in terms of two parameters: the nuclear reorganization energy (γ) and the electroniccoupling strength (H AB ). Studies of ET reactions in ruthenium-modified proteins have probed γ and H AB in several metalloproteins (cytochrome c, myoglobin, azurin). This work has shown that protein reorganization energies are sensitive to the medium surrounding the redox sites and that an aqueous environment, in particular, leads to large reorganization energies. Analyses of electronic-coupling strengths suggest that the efficiency of long-range ET depends on the protein secondary structure: β sheets appear to mediate coupling more efficiently than α-helical structures, and hydrogen bonds play a critical role in both.
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