谷胱甘肽
化学
部分
紧身衣
荧光
活性氧
吡啶
半胱氨酸
连接器
光化学
生物物理学
组合化学
生物化学
立体化学
有机化学
生物
物理
量子力学
计算机科学
酶
操作系统
作者
Jian Zhang,Xiaolong Bao,Junliang Zhou,Fangfang Peng,Hang Ren,Xiaochun Dong,Weili Zhao
标识
DOI:10.1016/j.bios.2016.05.005
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 109nM 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.
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