Bioluminescent Indicator for Highly Sensitive Analysis of Estrogenic Activity in a Cell-Based Format

被引:3
|
作者
Takenouchi, Osamu [1 ]
Kanno, Akira [1 ,2 ]
Takakura, Hideo [1 ,3 ]
Hattori, Mitsuru [1 ,4 ]
Ozawa, Takeaki [1 ]
机构
[1] Univ Tokyo, Sch Sci, Dept Chem, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1130033, Japan
[2] Toyama Univ, Fac Engn, Dept Environm Appl Chem, 3190 Gofuku, Toyama 9308555, Japan
[3] Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12,Nishi 6, Sapporo, Hokkaido 0600812, Japan
[4] Univ Fukui, Sch Med, Div Pharmacol, 23-3 Matsuokashimoaizuki, Eiheiji, Fukui 9101193, Japan
基金
日本学术振兴会;
关键词
PROTEIN-PROTEIN INTERACTIONS; RESONANCE ENERGY-TRANSFER; RECEPTORS ALPHA; FLUORESCENCE; BINDING; IMMUNOASSAY; CHEMICALS; DYNAMICS; MOTIF;
D O I
10.1021/acs.bioconjchem.6b00466
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Estrogens regulate different physiological systems with wide ranges of concentrations. The rapid analysis of estrogens is crucially important for drug discovery and medical diagnosis, but quantitation of nanomolar estrogens in live cells persists as an important challenge. We herein describe a bioluminescent indicator used to detect low concentrations of estrogens quantitatively with a high signal-to-background ratio. The indicator comprises a ligand-binding domain of an estrogen receptor connected with its binding peptide, which is sandwiched between split fragments of a luciferase mutant. Results show that the indicator recovered its bioluminescence upon binding to 17 beta-estradiol at concentrations higher than 1.0 x 10(-10) M. The indicator was reactive to agonists but did not respond to antagonists. The indicator is expected to be applicable for rapid screening estrogenic compounds and inhibitors, facilitating the discovery of drug candidates in a high-throughput manner.
引用
收藏
页码:2689 / 2694
页数:6
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