Discovery of Environment-Sensitive Fluorescent Agonists for α1-Adrenergic Receptors

被引:16
|
作者
Qin, Xiaojun [1 ]
Ma, Zhao [1 ,2 ]
Yang, Xingye [1 ]
Hu, Shilong [1 ]
Chen, Xinxin [1 ]
Liang, Dong [1 ]
Lin, Yuxing [1 ]
Shi, Xiaodong [3 ]
Du, Lupei [1 ]
Li, Minyong [1 ,4 ]
机构
[1] Shandong Univ, Sch Pharm, Dept Med Chem, Key Lab Chem Biol MOE, Jinan 250012, Shandong, Peoples R China
[2] Univ Calif Davis, UC Davis Comprehens Canc Ctr, Dept Biochem & Mol Med, Sacramento, CA 95817 USA
[3] Univ S Florida, Dept Chem, Tampa, FL 33620 USA
[4] Shandong Univ, State Key Lab Microbial Technol, Jinan 250100, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
LIGAND-BINDING; PROBES; SELECTIVITY; ACID; ANTAGONISTS; SUBTYPES; CELLS;
D O I
10.1021/acs.analchem.9b01059
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A series of novel fluorescent agonists were well developed herein with turn-on switch for alpha(1)-adrenergic receptors (alpha(1)-ARs) by conjugating the environment-sensitive fluorophore 4-chloro-7-nitrobenzoxadiazole with phenylephrine. Overall, these probes exhibited efficient binding and apparent fluorescence intensity changes (up to 10-fold) upon binding with alpha(1)-ARs. Moreover, these probes have been successfully applied for selectively imaging alpha(1)-ARs in the living cells. The dynamic process of alpha(1)-ARs internalization was traced successfully with these newly designed fluorescent agonists. Fluorescence polarization assay demonstrated specific interactions between these probes and alpha(1)-ARs. With these new probes, a bioluminescence resonance energy transfer binding assay has been well established and applied applied to the high-throughput screening of unlabeled alpha(1)-ARs agonist and antagonist. It is expected that these environment-sensitive fluorescent turn-on agonists may provide useful new tools in studying pharmacology and physiology of alpha(1)-ARs during drug discovery.
引用
收藏
页码:12173 / 12180
页数:8
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