| Literature DB >> 28492074 |
Huateng Zhang1, Jing Su2,3, Yuxin Lin1, Haixiu Bai1,4, Jiaxiang Liu1, Hui Chen1, Lupei Du1, Lichuan Gu2, Minyong Li1.
Abstract
Chalcone refers to an aromatic ketone and an enone that constitutes the central core for various important biological compounds in drug discovery. Moreover, the firefly luciferase (Fluc) as the bioluminescent reporter has been widely used in life science research and high-throughput screening (HTS). However, Fluc might suffer from direct inhibition by HTS compounds resulting in the occurrence of "false positives." In the current research, we discovered a series of chalcone compounds as Fluc inhibitors with favorable potency both in vitro and in vivo. Moreover, our compound 3i showed remarkable systemic inhibition in transgenic mice. Both enzymatic kinetics study and cocrystal structure demonstrated that compound 3i is competitive for substrate aminoluciferin, while noncompetitive for ATP. Besides, compound 3i exhibited excellent selectivity as a promising quenching agent in a simulated dual-luciferase reporter assay. We believed that our research would contribute to improving scientists' awareness of the Fluc inhibitors, pay attention to the bias results, and even expand the utilization of bioluminescence in life science research.Entities:
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Year: 2017 PMID: 28492074 DOI: 10.1021/acs.analchem.7b00813
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986