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Endoplasmic reticulum-targeted fluorogenic probe based on pyrimidine derivative for visualizing exogenous/endogenous H2S in living cells

机译:基于嘧啶衍生物的内质网靶向荧光探针,用于在活细胞中可视化外源/内源H2S的衍生物

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摘要

Developing new probes for visualizing H2S in the endoplasmic reticulum (ER) is of great significance in physiological and pathological fields in that the probe can antagonise ER stress. Herein, we try to explore efficient reporting fluorophores based on three pyrimidine derivatives (L1, L2 and L3), and eventually, a novel probe WH2S was fabricated by using emissive pyrimidine derivative (L1) as the reporting fluomphore. Upon the addition of H2S, the probe processed a thiolytic cleavage to regenerate L1, delivering a remarkable fluorescence enhancement. Probe WH2S presents a perfect selectivity, high sensitivity and low detection limit (3.81 mu M) towards H2S in the buffer media. Most importantly, fluorescence microscopy experiments demonstrate that WH2S can precisely accumulate in ER and detect exogenous/endogenous H2S at cellular level. These results imply that probe WH2S possesses great potentiality in tracking target H2S in complicated and changeable living systems.
机译:开发用于在内质网(ER)中的可视化H 2 S的新探针在生理和病理领域具有重要意义,因为探针可以拮抗ER应力。 在此,我们尝试基于三个嘧啶衍生物(L1,L2和L3)探索有效的报告荧光团,最终通过使用发光嘧啶衍生物(L1)作为报告荧光酚,通过使用发光嘧啶衍生物(L1)来制造新的探针WH2。 在加入H 2 S后,探针加工硫醇裂解至再生L1,递送显着的荧光增强。 探针WH2S在缓冲介质中呈现完美的选择性,高灵敏度和低检测限(3.81μm)。 最重要的是,荧光显微镜实验表明,WH2S可以精确地积聚在ER中并检测细胞水平的外源/内源H2。 这些结果意味着探针WH2S在复杂和可变的生活系统中跟踪目标H2S具有巨大潜力。

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