斯托克斯位移
荧光
荧光团
化学
半胱氨酸
近红外光谱
同型半胱氨酸
质子核磁共振
光化学
赫拉
检出限
分析化学(期刊)
生物物理学
立体化学
细胞
生物化学
光学
色谱法
酶
生物
物理
作者
Yin Ai,Haichang Ding,Congbin Fan,Gang Liu,Shouzhi Pu
标识
DOI:10.1016/j.dyepig.2022.110320
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 μM), 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 μM. 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.
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