A mitochondria-targeted turn-on fluorescent probe for the detection of glutathione in living cells

被引:113
|
作者
Zhang, Jian [1 ]
Bao, Xiaolong [1 ]
Zhou, Junliang [1 ]
Peng, Fangfang [2 ]
Ren, Hang [1 ]
Dong, Xiaochun [1 ]
Zhao, Weili [1 ,2 ]
机构
[1] Fudan Univ, Sch Pharm, Shanghai 201203, Peoples R China
[2] Henan Univ, Minist Educ, Key Lab Special Funct Mat, Kaifeng 475004, Peoples R China
来源
BIOSENSORS & BIOELECTRONICS | 2016年 / 85卷
基金
中国国家自然科学基金;
关键词
BODIPY; Fluorescent probe; Glutathione; Fluorescence imaging; Mitochondria-targeted; HIGHLY SELECTIVE DETECTION; RESTRICTED AZA-BODIPY; HYDROGEN-SULFIDE; CYSTEINE; HOMOCYSTEINE; SENSOR; GSH; PLASMA; CYS; DISCRIMINATION;
D O I
10.1016/j.bios.2016.05.005
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A novel turn-on red fluorescent BODIPY-based probe (Probe 1) for the detection of glutathione was developed. Such a probe carries a para-dinitrophenoxy benzyl pyridinium moiety at the meso position of a BODIPY dye as self-immolative linker. Probe 1 responds selectively to glutathione with the detection limit of 109 nM over other amino acids, common metal ions, reactive oxygen species, reactive nitrogen species, and reactive sulfur species. A novel electrostatic interaction to modulate the SNAr attack of glutathione was believed to play significant role for the observed selective response to glutathione. The cleavage of dinitrophenyl ether by glutathione leads to the production of para-hydroxybenzyl moiety which is able to self-immolate through an intramolecular 1,4-elimination reaction to release the fluorescent BODIPY dye. The low toxic probe has been successfully used to detect mitochondrial glutathione in living cells. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:164 / 170
页数:7
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