Gong Hao, Zhang Shuo, Ye Richard Dequan
Yao Xue Xue Bao. 2016 Dec;51(12):1829-37.
Since the Monod-Wyman-Changeux (MWC) model was initially proposed to explain the allosteric interactions between proteins and their ligands 50 years ago, there have been various models and hypotheses such as the induced-fit model on the interaction. These theoretical developments have been used broadly in the study of allosteric modulations of enzymes and receptors. In 1980, Lefkowitz and coworkers proposed a ternary complex model (TCM) for the regulatory mechanism of G protein-coupled receptors (GPCRs) that laid the theoretical foundation in the study of allosteric sites and ligands of GPCRs, the largest family of known receptors. The findings on how ligands interact with receptors to cause a functional response have significantly impacted the drug discovery field and accelerated the identification of allosteric modulators.
50年前,莫诺德-怀曼-尚热(MWC)模型最初被提出用于解释蛋白质与其配体之间的变构相互作用,此后出现了各种模型和假说,比如关于相互作用的诱导契合模型。这些理论进展已广泛应用于酶和受体变构调节的研究中。1980年,莱夫科维茨及其同事提出了一种用于G蛋白偶联受体(GPCR)调节机制的三元复合物模型(TCM),该模型为已知最大的受体家族GPCR的变构位点和配体研究奠定了理论基础。关于配体如何与受体相互作用以引发功能反应的研究结果对药物发现领域产生了重大影响,并加速了变构调节剂的鉴定。