首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Water-soluble gold nanoclusters prepared by protein-ligand interaction as fluorescent probe for real-time assay of pyrophosphatase activity
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Water-soluble gold nanoclusters prepared by protein-ligand interaction as fluorescent probe for real-time assay of pyrophosphatase activity

机译:通过蛋白质-配体相互作用制备的水溶性金纳米簇作为荧光探针实时测定焦磷酸酶活性

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This paper reports a new and facile method for the synthesis of water-soluble thiolate-protected AuNCs via protein-ligand interaction. Using 3-mercaptopropionic acid (MPA) as a model ligand and bovine serum albumin (BSA) as a model protein, water-soluble AuNCs (BSA/MPA-AuNCs) with intense orange yellow fluorescent emission (quantum yield = 16%) are obtained. Results show that AuNCs produced with this method have hydrophobic interactions with BSA. The synthetic strategy is then successfully extended to produce water-soluble AuNCs protected by other thiolates. Moreover, a sensitive and eco-friendly sensing system is established for detection of the activity of inorganic pyrophosphatase (PPase), which relies on the selective coordination of Fe3+ with BSA/MPA-AuNCs, the higher affinity between pyrophosphate (PPi) and Fe3+, and the hydrolysis of PPi by PPase. A good linearity between the fluorescence intensity and PPase activity within the range from 0.1 to 3 U/L. is found, with a detection limit down to 0.07 U/L. Additionally, the fluorescent assay developed here is utilized to assay the PPase activity in real biological samples and as well as to evaluate PPase inhibitor, illustrating the great potential for biological analysis. (C) 2016 Elsevier B.V. All rights reserved.
机译:本文报道了一种新的简便方法,可通过蛋白质-配体相互作用合成水溶性硫醇盐保护的AuNC。使用3-巯基丙酸(MPA)作为模型配体和牛血清白蛋白(BSA)作为模型蛋白,可得到具有强烈橙黄色荧光发射(量子产率= 16%)的水溶性AuNCs(BSA / MPA-AuNCs)。 。结果表明,用这种方法生产的AuNCs与BSA具有疏水相互作用。然后成功地扩展了合成策略,以生产受其他硫醇盐保护的水溶性AuNC。此外,建立了灵敏且环保的传感系统来检测无机焦磷酸酶(PPase)的活性,该系统依赖于Fe3 +与BSA / MPA-AuNCs的选择性配位,焦磷酸盐(PPi)与Fe3 +之间的亲和力更高,和PPase水解PPi。荧光强度和PPase活性之间的线性良好,范围为0.1至3 U / L。被发现,检测限低至0.07 U / L。此外,此处开发的荧光测定法可用于测定实际生物样品中的PPase活性,以及​​评估PPase抑制剂,从而说明了生物学分析的巨大潜力。 (C)2016 Elsevier B.V.保留所有权利。

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