Chen Jin, Zeng Lingyu, Xia Tian, Li Shuang, Yan Tengfei, Wu Song, Qiu Guofu, Liu Zhihong
†School of Pharmaceutical Sciences, ‡Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, and §College of Life Science, Wuhan University, Wuhan, Hubei 430072, China.
Anal Chem. 2015 Aug 18;87(16):8052-6. doi: 10.1021/acs.analchem.5b02032. Epub 2015 Jul 28.
Malondialdehyde (MDA) is a significant biomarker of oxidative stress. Variations of MDA level in biological systems often represent pathological changes that are related with many types of diseases. Although a variety of techniques have been developed for MDA detection, the probing of this biomarker in living cells remains unexplored. Herein, we report a turn-on fluorescent probe, MDAP-1, with a synergistic photoinduced electron transfer (PET)-hydrogen bonding mechanism, which for the first time realizes MDA sensing under physiological conditions with excellent sensitivity and specificity. The probe responds to MDA with a fluorescence enhancement factor (FEF) of up to >170-fold and a large Stokes shift (∼180 nm). Further biological evaluations show that MDAP-1 is able to detect both endogenous and exogenous MDA in living cells. It can be used to track the generation of MDA under oxidative stress, as stimulated by H2O2. We believe the results of this work will be helpful to the studies of MDA-related biological events and the elucidation of the underlying pathological mechanism in the future.
丙二醛(MDA)是氧化应激的重要生物标志物。生物系统中MDA水平的变化通常代表与多种疾病相关的病理变化。尽管已经开发了多种用于检测MDA的技术,但在活细胞中探测这种生物标志物仍未得到探索。在此,我们报告了一种具有协同光诱导电子转移(PET)-氢键机制的开启型荧光探针MDAP-1,它首次在生理条件下以优异的灵敏度和特异性实现了MDA传感。该探针对MDA的荧光增强因子(FEF)高达>170倍,斯托克斯位移大(约180 nm)。进一步的生物学评估表明,MDAP-1能够检测活细胞中的内源性和外源性MDA。它可用于追踪由H2O2刺激产生的氧化应激下MDA的生成。我们相信这项工作的结果将有助于未来对与MDA相关的生物事件的研究以及潜在病理机制的阐明。