Firefly Luciferase in Chemical Biology: A Compendium of Inhibitors, Mechanistic Evaluation of Chemotypes, and Suggested Use As a Reporter

被引:113
作者
Thorne, Natasha [1 ]
Shen, Min [1 ]
Lea, Wendy A. [1 ]
Simeonov, Anton [1 ]
Lovell, Scott [3 ]
Auld, Douglas S. [1 ]
Inglese, James [1 ,2 ]
机构
[1] Natl Ctr Advancing Translat Sci, Bethesda, MD 20892 USA
[2] Natl Human Genome Res Inst, NIH, Bethesda, MD 20892 USA
[3] Univ Kansas, Struct Biol Ctr, Lawrence, KS 66047 USA
来源
CHEMISTRY & BIOLOGY | 2012年 / 19卷 / 08期
基金
美国国家卫生研究院;
关键词
IDENTIFICATION; ASSAYS; BIOLUMINESCENCE; CELLS;
D O I
10.1016/j.chembiol.2012.07.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Firefly luciferase (FLuc) is frequently used as a reporter in high-throughput screening assays, owing to the exceptional sensitivity, dynamic range, and rapid measurement that bioluminescence affords. However, interaction of small molecules with FLuc has, to some extent, confounded its use in chemical biology and drug discovery. To identify and characterize chemotypes interacting with FLuc, we determined potency values for 360,864 compounds found in the NIH Molecular Libraries Small Molecule Repository, available in PubChem. FLuc inhibitory activity was observed for 12% of this library with discernible SAR. Characterization of 151 inhibitors demonstrated a variety of inhibition modes, including FLuc-catalyzed formation of multisubstrate adduct enzyme inhibitor complexes. As in some cell-based FLuc reporter assays, compounds acting as FLuc inhibitors yield paradoxical luminescence increases, thus data on compounds acquired from FLuc-dependent assays require careful analysis as described here.
引用
收藏
页码:1060 / 1072
页数:13
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