A red-emitting fluorescence turn-on probe for the discrimination of cysteine from biothiols and its bioimaging applications in living cells

被引:34
作者
Jiao, Shan [1 ,2 ]
He, Xu [4 ]
Xu, Longbin [1 ]
Ma, Pinyi [1 ]
Liu, Chunming [3 ]
Huang, Yibing [4 ]
Sun, Ying [1 ]
Wang, Xinghua [1 ]
Song, Daqian [1 ]
机构
[1] Jilin Univ, Coll Chem, Qianjin St 2699, Changchun 130012, Jilin, Peoples R China
[2] Jilin Univ, Endodont Dept, Stomatol Hosp, Qinghua Rd 1500, Changchun 130021, Jilin, Peoples R China
[3] Changchun Normal Univ, Cent Lab, 677 North Changji Rd, Changchun 130032, Jilin, Peoples R China
[4] Jilin Univ, Coll Life Sci, Qianjin St 2699, Changchun 130012, Jilin, Peoples R China
关键词
Fluorescent probe; Red-emitting; Cysteine; Endogenous; Living cells; HIGHLY SELECTIVE DETECTION; SENSOR; GLUTATHIONE; HOMOCYSTEINE; CONJUGATE; DESIGN; DOTS; CYS;
D O I
10.1016/j.snb.2019.03.119
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein, we synthesized a red-emitting fluorescence turn-on probe (HSA) for specific detection of cysteine (Cys) over other biothiols (glutathione (GSH) and homocysteine (Hcy)). The acrylate group was chosen as the recognition site for specific discrimination of Cys. Absorption and emission spectra display a high selectivity towards Cys over GSH/Hcy, organic small-molecule interfering substances and anions, with a high sensitivity towards Cys (0.12 mu M) in 1% ethanol-containing PBS buffer solution (25 mM, pH=7.4). Density functional theory (DFT) and time-dependent DFT (TDDFT) calculations were conducted to clarify the luminescence mechanism of the probe. Furthermore, the probe was successfully applied to the determination of free Cys in human serum and the fluorescence imaging of endogenous Cys in living cells.
引用
收藏
页码:47 / 52
页数:6
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