Coumarin-aurone based fluorescence probes for cysteine sensitive in-situ identification in living cells

被引:3
作者
Zhang, Yan [1 ]
Tang, Luyao [1 ]
Yang, Guiyi [1 ]
Xin, Haotian [1 ]
Huang, Yan [1 ]
Li, Keyi [1 ]
Liu, Jiandong [2 ,3 ]
Pang, Jiaojiao [2 ,3 ]
Cao, Duxia [1 ]
机构
[1] Univ Jinan, Sch Mat Sci & Engn, Jinan, Peoples R China
[2] Shandong Univ, Dept Emergency Med, Qilu Hosp, Jinan, Peoples R China
[3] Shandong Univ, Shandong Prov Clin Res Ctr Emergency & Crit Care M, Med & Pharmaceut Basic Res Innovat Ctr Emergency &, NMPA Key Lab Clin Res & Evaluat Innovat Drug,Shand, Jinan, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescent probe; Coumarin; Aurone; Cysteine; Imaging; HOMOCYSTEINE; GLUTATHIONE;
D O I
10.1016/j.colsurfb.2024.114173
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The quantification of cysteine (Cys) levels in the organisms holds paramount significance in biological research and disease diagnosis, which can give the correlation between abnormal Cys levels and diseases. In this study, two fluorescent probes, designated as DEA-OH and DEA-AC, featuring a coumarin-aurone backbone specifically engineered for Cys detection, were meticulously designed and synthesized. The diethylamino coumarin-aurone probe DEA-OH and the acrylate-substituted probe DEA-AC demonstrated remarkable sensitivity in detecting cysteine by means of copper displacement (DEA-OH) and acrylate hydrolysis mechanisms (DEA-AC) with fluorescence detection limits of 7.25 mu M and 1.65 mu M, respectively. Moreover, the fluorescence peak wavelength of the two probes displayed a linear relationship with solvent polarity in the ET (30) range of 30-65 kcal center dot mol- 1, indicating the potential for monitoring changes in environmental polarity within this ET (30) range. The outstanding attributes exhibited by DEA-AC including superior photostability, remarkable selectivity, and swift response (kinetic rate constant: 0.00747 s- 1), coupled with the exceptional anti-interference ability, have significantly broadened its scope of applications, for example detecting alterations in Cys within biological systems.
引用
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页数:7
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