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Fluorogenic Biosensors Constructed via Aggregation-induced Emission Based on Enzyme-catalyzed Coupling Reactions for Detection of Hydrogen Peroxide

机译:通过基于酶催化的偶联反应的酶催化偶联反应构建的荧光生物传感器,用于检测过氧化氢

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Hydrogen peroxide (H_(2)O_(2)) is a main reactive oxygen by-product produced in the metabolism of organisms and a common biomarker of oxidative stress. Aggregation-induced emission (AIE) probes for H_(2)O_(2) have been proposed. Such AIEgens mostly use benzeneboronic acid as a recognition group. Recently, a strategy involving enzyme-catalyzed polymerization of AIE compounds shows great potential in AIEgens design. We herein modify the AIE motif, tetraphenylethene (TPE) with o -phenylenediamine (TPE-TAF), which can be oxidated by H_(2)O_(2) in HRP to form an intramolecular phenazine structure. Compared with a similar approach, the proposed strategy is simple and the TPE-TAF showed a sensitive “turn-on” fluorescence with H_(2)O_(2). The detection limit (LOD) is 3.39 μM and the probe is highly specific against H_(2)O_(2). We further verified the reaction mechanism of the enzyme-catalyzed coupling reaction. The probe is a promising candidate as a stable and safe fluorescent substrate in H_(2)O_(2) sensing.
机译:过氧化氢(H_(2)O_(2))是在生物体代谢和氧化应激的常见生物标志物中产生的主要反应性氧副产物。已经提出了对H_(2)O_(2)的聚集诱导的发射(AIE)探针。这种辅助大多数使用苯硼酸作为识别组。最近,涉及AIE化合物的酶催化聚合的策略显示出抗血管设计的巨大潜力。我们在本文中修改AIE基序,用o-苯二胺(TPE-TAF)的四苯基乙烯(TPE),其可以通过HRP中的H_(2)O_(2)氧化以形成分子内苯脲素结构。与类似的方法相比,所提出的策略很简单,TPE-TAF显示敏感的“开启”荧光,具有H_(2)O_(2)。检测限(LOD)为3.39μm,探针对H_(2)O_(2)具有高度特异性。我们进一步验证了酶催化的偶联反应的反应机理。探针是具有H_(2)O_(2)感测的稳定和安全的荧光基底的承诺候选者。

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