Time-dependent NIR fluorescent probe with large Stokes-shift for detecting Cys/Hcy and cell imaging

被引:14
|
作者
Ai, Yin [1 ]
Ding, Haichang [1 ]
Fan, Congbin [1 ]
Liu, Gang [1 ]
Pu, Shouzhi [1 ,2 ]
机构
[1] Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Peoples R China
[2] Yuzhang Normal Univ, Dept Ecol & Environm, Nanchang 330103, Peoples R China
基金
中国国家自然科学基金;
关键词
NIR; Fluorescence probe; Cys; Hcy; Cell imaging; HIGHLY SELECTIVE DETECTION; LIVING CELLS; IN-VIVO; DISCRIMINATIVE DETECTION; CYSTEINE; CYS; GSH; HCY; CONJUGATE; DESIGN;
D O I
10.1016/j.dyepig.2022.110320
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Detection and imaging of Cysteine (Cys) and Homocysteine (Hcy) in living systems have drawn extensive attention over the years due to their significant biological role. However, few fluorescence probes have been reported to distinguish Cys and Hcy in near-infrared (NIR) range. In this paper, an original NIR Cys and Hcy fluorescent probe, namely DTRN, was synthesized. DTRN was constructed by using an acryloyl ester group as a trigger and dicyanoisophorone-derived as the fluorophore unit, it was found to emit NIR fluorescence with a 718 nm emission and have large stokes shift (~176 nm). DTRN hold excellent performances such as ultrasensitivity (LOD = 0.09 mu M), high specificity and fast response (< 2 min) for Cys. Distinctly, after Hcy was introduced, the emission intensity of DTRN at 718 nm must take 20 min to reach a plateau and the LOD was found to be 0.12 mu M. The sensing mechanism for Cys and Hcy in C2H5OH/PBS (4/6, v/v, pH = 7.4) was studied by 1H NMR spectroscopy and HRMS. Most importantly, the ability of DTRN to detect Cys in HeLa cells had also been achieved.
引用
收藏
页数:8
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