A Native-Chemical-Ligation-Based Turn-on Fluorescent Probe for Selective Detection of Cysteine

被引:8
|
作者
Shimizu, Masaki [1 ]
Fukui, Hiroki [1 ]
Shigitani, Ryosuke [1 ]
机构
[1] Kyoto Inst Technol, Fac Mol Chem & Engn, Sakyo Ku, 1 Hashikami Cho, Kyoto 6068585, Japan
关键词
Fluorescence; Sensing; Thiols; SOLID-STATE; LIVING CELLS; REACTIVE PROBES; HOMOCYSTEINE; EMISSION; GLUTATHIONE; PROTEINS; SENSOR; THIOL; CHEMOSENSORS;
D O I
10.1002/jccs.201500466
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Selective and quantitative detection of biological thiols such as cysteine, homocysteine, and glutathione is often necessary because abnormal levels of such thiols can cause some diseases. Here, we report that bis(pentafluorophenyl) 1,4-benzenedicarbothionic acid diester can serve as a turn-on fluorescent probe for selective detection of cysteine vis-a-vis homocysteine and glutathione. When cysteine was added to a mixture of the diester and a sodium phosphate buffer solution with THF (60 vol%), which is non-fluorescent, the mixture became green-fluorescent. In contrast, addition of homocysteine or glutathione did not make the mixture fluorescent. A native-chemical-ligation-based mechanism is proposed.
引用
收藏
页码:317 / 322
页数:6
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