化学
反硫化
荧光
癌细胞
半胱氨酸
生物化学
硫化氢
生物物理学
分析物
表观基因组
癌症
内生
代谢途径
代谢活性
细胞内
共焦
癌症研究
亚硫酸氢盐
胱硫醚β合酶
串扰
作者
Xin Jiang,Bo Liu,Yang Li,H. -Y. Jin,Tianpeng Zhong,Ting Yu,Han Tang,Xiaorui Liu,Danqing Xu,Yuquan Tang,Youyu Zhang,Haitao Li,Huijun Zhou,Yin Peng
标识
DOI:10.1016/j.saa.2025.127025
摘要
Early and accurate cancer diagnosis is essential for improving patient prognosis and guiding effective treatment. Metabolic reprogramming of the transsulfuration pathway is a hallmark of malignancy, characterized by elevated intracellular levels of cysteine (Cys), sulfur dioxide (SO₂), and hydrogen sulfide (H₂S). Here, we report the design and synthesis of TAC, a coumarin-based triple-channel fluorescent probe incorporating three distinct reactive sites for the simultaneous detection of Cys, SO₂, and H₂S. TAC exhibits high sensitivity, excellent selectivity, robust photostability, and negligible spectral crosstalk among the three emission channels. In live-cell imaging, TAC enabled real-time visualization of both endogenous and exogenous analytes with high spatial-temporal resolution. Importantly, TAC accurately discriminated between normal and cancer cells by capturing their distinct sulfur metabolic fingerprints, with cancer cells exhibiting significantly higher fluorescence in all channels. This work introduces the first fluorescent probe capable of triple-analyte imaging within the transsulfuration pathway, providing a powerful platform for non-invasive metabolic profiling and early cancer screening.
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