Department of Medicinal Chemistry, Key Laboratory of Chemical Biology (MOE), School of Pharmacy, Shandong University , Jinan, Shandong 250012, China.
State Key Laboratory of Microbial Technology, School of Life Sciences, Shandong University , Jinan, Shandong 250100, China.
Anal Chem. 2017 Jun 6;89(11):6099-6105. doi: 10.1021/acs.analchem.7b00813. Epub 2017 May 23.
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.
查耳酮是一种芳香酮和烯酮,构成了药物发现中各种重要生物化合物的核心结构。此外,萤火虫荧光素酶(Fluc)作为生物发光报告酶已被广泛应用于生命科学研究和高通量筛选(HTS)。然而,Fluc 可能会受到 HTS 化合物的直接抑制,从而导致“假阳性”的发生。在当前的研究中,我们发现了一系列查尔酮化合物,它们对 Fluc 具有良好的体外和体内抑制活性。此外,我们的化合物 3i 在转基因小鼠中表现出显著的全身抑制作用。酶动力学研究和共晶结构表明,化合物 3i 是底物氨基萤光素的竞争性抑制剂,而对 ATP 是非竞争性抑制剂。此外,化合物 3i 在模拟双荧光素酶报告基因检测中表现出优异的选择性,作为一种有前途的淬灭剂。我们相信,我们的研究将有助于提高科学家对 Fluc 抑制剂的认识,关注偏倚结果,甚至扩大生物发光在生命科学研究中的应用。