Singh Anchal, Gao Mingze, Beck Michael W
Department of Chemistry and Biochemistry, Eastern Illinois University Charleston IL 61920 USA
Department of Biological Sciences, Eastern Illinois University Charleston IL 61920 USA.
RSC Med Chem. 2021 May 18;12(7):1142-1153. doi: 10.1039/d1md00073j. eCollection 2021 Jul 21.
Human carboxylesterases (CESs) are serine hydrolases that are responsible for the phase I metabolism of an assortment of ester, amide, thioester, carbonate, and carbamate containing drugs. CES activity is known to be influenced by a variety of factors including single nucleotide polymorphisms, alternative splicing, and drug-drug interactions. These different factors contribute to interindividual variability of CES activity which has been demonstrated to influence clinical outcomes among people treated with CES-substrate therapeutics. Detailed exploration of the factors that influence CES activity is emerging as an important area of research. The use of fluorescent probes with live cell imaging techniques can selectively visualize the real-time activity of CESs and have the potential to be useful tools to help reveal the impacts of CES activity variations on human health. This review summarizes the properties of the five known human CESs including factors reported to or that could potentially influence their activity before discussing the design aspects and use considerations of CES fluorescent probes in general in addition to highlighting several well-characterized probes.
人类羧酸酯酶(CESs)是丝氨酸水解酶,负责对多种含酯、酰胺、硫酯、碳酸酯和氨基甲酸酯的药物进行I相代谢。已知CES活性受多种因素影响,包括单核苷酸多态性、可变剪接和药物相互作用。这些不同因素导致CES活性的个体间差异,已证明这种差异会影响接受CES底物治疗的患者的临床结局。对影响CES活性的因素进行详细探索正成为一个重要的研究领域。将荧光探针与活细胞成像技术结合使用,可以选择性地可视化CESs的实时活性,并有潜力成为有助于揭示CES活性变化对人类健康影响的有用工具。本综述总结了五种已知人类CESs的特性,包括据报道或可能影响其活性的因素,然后讨论了CES荧光探针的一般设计方面和使用注意事项,此外还重点介绍了几种特征明确的探针。