Biological Phosphoryl-Transfer Reactions: Understanding Mechanism and Catalysis

被引:316
作者
Lassila, Jonathan K. [1 ]
Zalatan, Jesse G. [2 ]
Herschlag, Daniel [1 ]
机构
[1] Stanford Univ, Dept Biochem, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Dept Mol & Cellular Pharmacol, San Francisco, CA 94158 USA
来源
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 80 | 2011年 / 80卷
关键词
transition state; enzymes; linear free energy relationship; kinetic isotope effects; phosphate ester; TRANSITION-STATE STRUCTURES; PROTEIN-TYROSINE-PHOSPHATASE; P-NITROPHENYL PHOSPHATE; TETRAHYMENA RIBOZYME REACTION; SULFURYL TRANSFER-REACTIONS; COLI ALKALINE-PHOSPHATASE; LEAVING-GROUP DEPENDENCE; ACID-BASE CATALYSIS; ENZYME ACTIVE-SITE; METAL-ION;
D O I
10.1146/annurev-biochem-060409-092741
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
Phosphoryl-transfer reactions are central to biology. These reactions also have some of the slowest nonenzymatic rates and thus require enormous rate accelerations from biological catalysts. Despite the central importance of phosphoryl transfer and the fascinating catalytic challenges it presents, substantial confusion persists about the properties of these reactions. This confusion exists despite decades of research on the chemical mechanisms underlying these reactions. Here we review phosphoryl-transfer reactions with the goal of providing the reader with the conceptual and experimental background to understand this body of work, to evaluate new results and proposals, and to apply this understanding to enzymes. We describe likely resolutions to some controversies, while emphasizing the limits of our current approaches and understanding. We apply this understanding to enzyme-catalyzed phosphoryl transfer and provide illustrative examples of how this mechanistic background can guide and deepen our understanding of enzymes and their mechanisms of action. Finally, we present important future challenges for this field.
引用
收藏
页码:669 / 702
页数:34
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