A Phenylselenium-Substituted BODIPY Fluorescent Turn-off Probe for Fluorescence Imaging of Hydrogen Sulfide in Living Cells

被引:72
作者
Gong, Deyan [1 ,2 ]
Zhu, Xiangtao [3 ,4 ]
Tian, Yuejun [5 ]
Han, Shi-Chong [3 ,4 ]
Deng, Min [1 ,2 ]
Iqbal, Anam [1 ,2 ]
Liu, Weisheng [1 ,2 ]
Qin, Wenwu [1 ,2 ]
Guo, Huichen [3 ,4 ]
机构
[1] Lanzhou Univ, Key Lab Nonferrous Met Chem & Resources Utilizat, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
[2] Lanzhou Univ, State Key Lab Appl Organ Chem, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
[3] Chinese Acad Agr Sci, State Key Lab Vet Etiol Biol, Xujiaping 1, Lanzhou 730046, Gansu, Peoples R China
[4] Chinese Acad Agr Sci, Key Lab Anim Virol, Minist Agr, Lanzhou Vet Res Inst, Xujiaping 1, Lanzhou 730046, Gansu, Peoples R China
[5] Lanzhou Univ, Hosp 2, Inst Urol, Lanzhou, Gansu, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
SE-N BOND; SENSOR; GLUTATHIONE; THIOLS; DYES; TIME;
D O I
10.1021/acs.analchem.6b04114
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein a phenylselenium-substituted BODIPY (1) fluorescent turn-off sensor was developed for the purpose to achieve excellent selectivity and sensitivity for H2S detection based on the substitution reaction of the phenylselenide group at the 3-position with H2S. The excess addition of hydrogen sulfide promoted further substitution of the phenylselenide group at the 5-position of the probe and was accompanied by a further decrease in fluorescence emission intensity. Sensor 1 demonstrated remarkable performance with 49-fold red color fluorescence intensity decrease at longer excitation wavelength, a low detection limit (0.0025 mu M), and specific fluorescent response toward H2S over anions, biothiols, and other amino acids in neutral media. It showed no obvious cell toxicity and good membrane permeability, which was well exploited for intracellular H2S detection and imaging through fluorescence microscopy imaging.
引用
收藏
页码:1801 / 1807
页数:7
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