Laboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University, New York, New York 10065, United States.
Departments of Immunology and Microbiology, Chemistry, Scripps Research, La Jolla, California 92037, United States.
ACS Chem Biol. 2020 Sep 18;15(9):2324-2330. doi: 10.1021/acschembio.0c00432. Epub 2020 Sep 10.
The characterization of specific metabolite-protein interactions is important in chemical biology and drug discovery. For example, nuclear receptors (NRs) are a family of ligand-activated transcription factors that regulate diverse physiological processes in animals and are key targets for therapeutic development. However, the identification and characterization of physiological ligands for many NRs remains challenging, because of limitations in domain-specific analysis of ligand binding in cells. To address these limitations, we developed a domain-specific covalent chemical reporter for peroxisome proliferator-activated receptors (PPARs) and demonstrated its utility to screen and characterize the potency of candidate NR ligands in live cells. These studies demonstrate targeted and domain-specific chemical reporters provide excellent tools to evaluate endogenous and exogenous (diet, microbiota, therapeutics) ligands of PPARs in mammalian cells, as well as additional protein targets for further investigation.
特定代谢物-蛋白质相互作用的特征在化学生物学和药物发现中很重要。例如,核受体 (NRs) 是一类配体激活的转录因子,它们调节动物体内的多种生理过程,是治疗开发的关键靶点。然而,由于细胞内配体结合的特定域分析存在局限性,许多 NRs 的生理配体的鉴定和特征描述仍然具有挑战性。为了解决这些限制,我们开发了一种针对过氧化物酶体增殖物激活受体 (PPARs) 的特定域共价化学报告物,并证明其可用于筛选和表征活细胞中候选 NR 配体的效力。这些研究表明,靶向和特定域的化学报告物为评估哺乳动物细胞中 PPARs 的内源性和外源性(饮食、微生物群、治疗剂)配体以及其他蛋白质靶标提供了极好的工具,可进一步进行研究。