A water-soluble and incubate-free fluorescent environment-sensitive probe for ultrafast visualization of protein thiols within living cells

被引:15
作者
Li, Xiaolu [1 ,2 ]
Feng, Qian [1 ,2 ]
Qu, Lejing [1 ,2 ]
Zhao, Ting [1 ]
Li, Xiaoan [1 ,2 ]
Bai, Tiantian [1 ,2 ]
Sun, Shisheng [1 ]
Wu, Shaoping [1 ,2 ]
Zhang, Yongmin [1 ,2 ,3 ]
Li, Jianli [4 ]
机构
[1] Northwest Univ, Minist Educ, Biomed Key Lab Shaanxi Prov, Key Lab Resource Biol & Biotechnol Western China, Xian 710069, Peoples R China
[2] Northwest Univ, Joint Int Lab Glycobiol & Med Chem, Xian 710069, Shaanxi, Peoples R China
[3] Sorbonne Univ, CNRS, UMR 8232, Inst Parisien Chim Mol, 4 Pl Jussieu, F-75005 Paris, France
[4] Northwest Univ, Coll Chem & Mat Sci, Minist Educ, Key Lab Synthet & Nat Funct Mol Chem, Xian 710127, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Environment-sensitive; Fluorescent probe; Protein thiols; Coumarin; BSA; Bioimaging; PERFORMANCE LIQUID-CHROMATOGRAPHY; CAPILLARY-ELECTROPHORESIS; FLUOROGENIC REAGENT; OXIDATIVE STRESS; PLASMA; GLUTATHIONE; CYSTEINE; ALBUMIN; DESIGN;
D O I
10.1016/j.aca.2020.06.026
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The amount of protein thiols play a crucial role in maintaining the cellular redox homeostasis and have significant implications to indicate a series of diseases. Therefore, it is necessary to develop an ideal probe for protein thiol detection in a simple and readily implementable method. Consequently, a water-soluble and incubate-free fluorescent environment-sensitive probe DMTs-OCC was synthesized using 7-diethylamincoumarin as the fluorophore and 4-(5-Methanesulfonyl- [1,2,3,4]tetrazol-1-yl)-phenol (MSTP) as a thiol receptor reagent. The blue-shift emission spectra of probe DMTs-OCC was observed by ultrafast binding to protein sulfhydryl groups from the excited intramolecular charge transfer (ICT) to the twisted intramolecular charge transfer (TICT) conversion process in aqueous solution. The experimental results showed that probe DMTs-OCC exhibited an excellent selectivity to protein thiols and biocompatibility in aqueous solution, as well as terrific cell membrane permeability which enabled the successful visualization of BSA protein thiol in living cells. Moreover, no excess probe was cleaned and no incubation time was needed in cell experiments. Therefore, it could provide a new method to the construction of fluorescent probes for protein thiols labelling and visualization. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:72 / 81
页数:10
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