Lampe Jed N
Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical CenterKansas City, MO, United States.
Front Pharmacol. 2017 Aug 8;8:521. doi: 10.3389/fphar.2017.00521. eCollection 2017.
In recent years, a growing appreciation has developed for the importance of protein-protein interactions to modulate the function of drug metabolizing enzymes. Accompanied with this appreciation, new methods and technologies have been designed for analyzing protein-protein interactions both and . These technologies have been applied to several classes of drug metabolizing enzymes, including: cytochrome P450's (CYPs), monoamine oxidases (MAOs), UDP-glucuronosyltransferases (UGTs), glutathione S-transferases (GSTs), and sulfotransferases (SULTs). In this review, we offer a brief description and assessment of the impact of many of these technologies to the study of protein-protein interactions in drug disposition. The still expanding list of these techniques and assays has the potential to revolutionize our understanding of how these enzymes carry out their important functions .
近年来,人们越来越认识到蛋白质 - 蛋白质相互作用对调节药物代谢酶功能的重要性。伴随着这种认识,已经设计出了用于分析蛋白质 - 蛋白质相互作用的新方法和技术。这些技术已应用于几类药物代谢酶,包括:细胞色素P450(CYPs)、单胺氧化酶(MAOs)、尿苷二磷酸葡萄糖醛酸基转移酶(UGTs)、谷胱甘肽S - 转移酶(GSTs)和磺基转移酶(SULTs)。在本综述中,我们简要描述并评估了其中许多技术对药物处置中蛋白质 - 蛋白质相互作用研究的影响。这些技术和检测方法的清单仍在不断扩大,有可能彻底改变我们对这些酶如何执行其重要功能的理解。