Factors influencing the energetics of electron and proton transfers in proteins. What can be learned from calculations?

被引:83
作者
Gunner, M. R. [1 ]
Mao, Junjun [1 ]
Song, Yifan [1 ]
Kim, Jinrang [1 ]
机构
[1] CUNY City Coll, Dept Phys, New York, NY 10031 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2006年 / 1757卷 / 08期
关键词
electrostatics; electrochemistry; pK(a); E-m; bacteriorhodopsin; simulation; bioenergetics;
D O I
10.1016/j.bbabio.2006.06.005
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
A protein structure should provide the information needed to understand its observed properties. Significant progress has been made in developing accurate calculations of acid/base and oxidation/reduction reactions in proteins. Current methods and their strengths and weaknesses are discussed. The distribution and calculated ionization states in a survey of proteins is described, showing that a significant minority of acidic and basic residues are buried in the protein and that most of these remain ionized. The electrochemistry of heme and quinones are considered. Proton transfers in bacteriorhodopsin and coupled electron and proton transfers in photosynthetic reaction centers, 5-coordinate heme binding proteins and cytochrome c oxidase are highlighted as systems where calculations have provided insight into the reaction mechanism. (c) 2006 Published by Elsevier B.V.
引用
收藏
页码:942 / 968
页数:27
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