Department of Chemistry and Biochemistry, Eastern Illinois University, Charleston, IL, 61920, USA.
Department of Biological Sciences, Eastern Illinois University, Charleston, IL, 61920, USA.
Chembiochem. 2022 Jun 20;23(12):e202200069. doi: 10.1002/cbic.202200069. Epub 2022 Mar 21.
Carboxylesterase 1 (CES1) plays a key role in the metabolism of endogenous biomolecules and xenobiotics including a variety of pharmaceuticals. Despite the established importance of CES1 in drug metabolism, methods to study factors that can vary CES1 activity are limited with only a few suitable for use in live cells. Herein, we report the development of FCP1, a new CES1 specific fluorescent probe with a unique carbonate substrate constructed from commercially available reagents. We show that FCP-1 can specifically report on endogenous CES1 activity with a robust fluorescence response in live HepG2 cells through studies with inhibitors and genetic knockdowns. Subsequently, we deployed FCP-1 to develop a live cell fluorescence microscopy-based approach to identify activity differences between CES1 isoforms. To the best of our knowledge, this is the first application of a fluorescent probe to measure the activity of CES1 sequence variants in live cells.
羧酸酯酶 1(CES1)在包括各种药物在内的内源性生物分子和外源性化学物质的代谢中发挥关键作用。尽管 CES1 在药物代谢中的重要性已得到确立,但目前用于研究可改变 CES1 活性的因素的方法有限,只有少数方法适用于活细胞。在此,我们报告了 FCP1 的开发,这是一种新的 CES1 特异性荧光探针,其独特的碳酸盐底物由市售试剂构建。我们通过抑制剂和基因敲低研究表明,FCP-1 可以在活 HepG2 细胞中通过强大的荧光反应特异性报告内源性 CES1 活性。随后,我们利用 FCP-1 开发了一种基于活细胞荧光显微镜的方法,以确定 CES1 同工型之间的活性差异。据我们所知,这是首次应用荧光探针来测量活细胞中 CES1 序列变异体的活性。