Proton-coupled electron transfer: a unifying mechanism for biological charge transport, amino acid radical initiation and propagation, and bond making/breaking reactions of water and oxygen

被引:169
作者
Chang, CJ [1 ]
Chang, MCY [1 ]
Damrauer, NH [1 ]
Nocera, DG [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2004年 / 1655卷 / 1-3期
关键词
proton-coulpled electron transfer; tyrosyl radical; oxygen and water activation; cytochrome c oxidase; Photosystem II; ribonucleotide reductase; monooxygenase; catalase; pacman; hangman; porphyrin; hydrogen-bonding; heme water channel; dagwoods;
D O I
10.1016/j.bbabio.2003.08.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Redox-driven proton pumps, radical initiation and propagation in biology, and small-molecule activation processes all involve the coupling of electron transfer to proton transport. A mechanistic frame work in which to interpret these processes is being developed by examining proton-coupled electron transfer (PCET) in model and natural systems. Specifically, PCET investigations are underway on the following three fronts: (I) the elucidation of the PCET reaction mechanism by time-resolved laser spectroscopy of electron donors and acceptors juxtaposed by a proton transfer interface; (2) the role of amino acid radicals in biological catalysis with the radical initiation and transport processes of E. coli ribonucleotide reductase (RNR) as a focal point; and (3) the application of PCET towards small-molecule activation with emphasis on biologically relevant bond-breaking and bond-making processes involving oxygen and water. A review of recent developments in each of these areas is discussed. (C) 2004 Elsevier B.V. All rights reserved.
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页码:13 / 28
页数:16
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