亲缘关系
化学
蛋白质配体
能量学
分子
小分子
结合亲和力
配体(生物化学)
熵(时间箭头)
焓
构象熵
计算化学
立体化学
热力学
生物化学
物理
受体
有机化学
作者
Stephen F. Martin,John H. Clements
标识
DOI:10.1146/annurev-biochem-060410-105819
摘要
Predicting protein-binding affinities of small molecules, even closely related ones, is a formidable challenge in biomolecular recognition and medicinal chemistry. A thermodynamic approach to optimizing affinity in protein-ligand interactions requires knowledge and understanding of how altering the structure of a small molecule will be manifested in protein-binding enthalpy and entropy changes; however, there is a relative paucity of such detailed information. In this review, we examine two strategies commonly used to increase ligand potency. The first of these involves introducing a cyclic constraint to preorganize a small molecule in its biologically active conformation, and the second entails adding nonpolar groups to a molecule to increase the amount of hydrophobic surface that is buried upon binding. Both of these approaches are motivated by paradigms suggesting that protein-binding entropy changes should become more favorable, but paradoxes can emerge that defy conventional wisdom.
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