Red emission cysteine probe with high selectivity based on fluorescent protein chromophores and turn-on fluorescence in cell cultures

被引:19
|
作者
Shen, Baoxing [1 ]
Qian, Ying [1 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Nanjing 211189, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescent protein; Cysteine; High selectivity; Red emission; Living cell imaging; LIVING CELLS; RHODAMINE-BODIPY; RAPID DETECTION; GLUTATHIONE; HOMOCYSTEINE; DISCRIMINATION; CHEMODOSIMETER; BIOTHIOLS; CYS; GFP;
D O I
10.1016/j.dyepig.2019.03.034
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Cysteine (Cys) plays a vital role in many physiological processes, and also is closely related to various diseases, thus the development of novel high selectivity and sensitivity fluorescent probes for in situ monitoring of biothiol (Cys) is crucial. Herein, we present a fluorogenic method to detect Cys in vitro and live cells based on fluorescent protein chromophores, which have been modulated by chemical reaction. Probe (RFP) is a fluorescence turn on probe with red emission wavelength and large Stokes shift (127 nm). This Michael-addition reaction-based probe exhibits low detection limit (18.7 mu M), fast response time, and low cytotoxicity. RFP can differentiate the Cys and Hcy, using the difference of reaction time between probe and Cys or Hcy. Together, this probe exhibited excellent cell permeability, and can be successfully applied to detect the endogenous Cys in living cells.
引用
收藏
页码:350 / 356
页数:7
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