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Functionalized Carbon Quantum Dots with Dopamine for Tyrosinase Activity Monitoring and Inhibitor Screening: In Vitro and Intracellular Investigation

机译:功能化的碳量子点与多巴胺的酪氨酸酶活性监测和抑制剂筛选:体外和细胞内研究

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摘要

Sensitive assay of tyrosinase (TYR) activity is in urgent demand for both fundamental research and practical application, but the exploration of functional materials with good biocompatibility for its activity evaluation at the intracellular level is still challenging until now. In this work, we develop a convenient and real-time assay with high sensitivity for TYR activity/level monitoring and its inhibitor screening based on biocompatible dopamine functionalized carbon quantum dots (Dopa-CQDs). Dopamine with redox property was functionalized on the surface of carbon quantum dots to construct a Dopa-CQDs conjugate with strong bluish green fluorescence. When the dopamine moiety in Dopa-CQDs conjugate was oxidized to a dopaquinone derivative under specific catalysis of TYR, an intrapartide photoinduced electron transfer (PET) process between CQDs and dopaquinone moiety took place, and then the fluorescence of the conjugate could be quenched simultaneously. Quantitative evaluation of TYR activity was established in terms of the relationship between fluorescence quenching efficiency and TYR activity. The assay covered a broad linear range of up to 800 U/L with a low detection limit of 7.0 U/L. Arbutin, a typical inhibitor of TYR, was chosen as an example to assess its function of inhibitor screening, and positive results were observed that fluorescence quenching extent of the probe was reduced in the presence of arbutin. It is also demonstrated that Dopa-CQD conjugate possesses excellent biocompatibility, and can sensitively monitor intracellular tyrosinase level in melanoma cells and intracellular pH changes in living cells, which provides great potential in application of TYR/pH-associated disease monitoring and medical diagnostics.
机译:酪氨酸酶(TYR)活性的灵敏测定是基础研究和实际应用的迫切需求,但是迄今为止,在细胞内水平上探索具有良好生物相容性的功能材料以进行活性评估仍是一项挑战。在这项工作中,我们基于生物相容性多巴胺功能化的碳量子点(Dopa-CQDs),开发了一种对TYR活性/水平监测及其抑制剂筛选具有高灵敏度的便捷实时测定法。将具有氧化还原特性的多巴胺在碳量子点的表面上官能化,以构建具有强烈蓝绿色荧光的Dopa-CQDs共轭物。在TYR的特异性催化下,当Dopa-CQDs共轭物中的多巴胺部分被氧化为多巴醌衍生物时,CQDs和多巴醌部分之间发生了部分光诱导电子转移(PET)过程,然后可以同时猝灭共轭物的荧光。根据荧光猝灭效率和TYR活性之间的关系建立了对TYR活性的定量评价。该测定法涵盖了高达800 U / L的宽线性范围,检测限为7.0 U / L。以典型的TYR抑制剂熊果苷为例,评估其抑制剂筛选的功能,并观察到阳性结果,在熊果苷存在下探针的荧光猝灭程度降低。还证明了Dopa-CQD缀合物具有优异的生物相容性,并且可以灵敏地监测黑素瘤细胞中的细胞内酪氨酸酶水平和活细胞中的细胞内pH变化,这在与TYR / pH相关的疾病监测和医学诊断中的应用具有巨大潜力。

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