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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Signal-on CoA-dependent electrochemical biosensor for highly sensitive and label-free detection of Citrate synthase activity
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Signal-on CoA-dependent electrochemical biosensor for highly sensitive and label-free detection of Citrate synthase activity

机译:信号依赖于CoA的电化学生物传感器,用于柠檬酸合酶活性的高灵敏度和无标记检测

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We report here a label-free and sensitive electrochemical method for probing Citrate synthase (CS) activity based on detailed investigations into the nucleic acid-mimicking coordination polymer (CP) formed from the coenzyme A (CoA)-Ag(I) repeat units. Our biosensing approach provides an especial and significant detection mechanism: CS can catalyze the essential condensation reaction between acetyl coenzyme A (Ac-CoA) and oxaloacetate (OAA) to form citrate and CoA; then, in the presence of Ag(I), CoA-Ag(I) CP can be in situ formed because of the strong complexation ability of thiol groups of CoA toward Ag(I). The generated CoA-Ag(I) CP attaches to graphene-modified glassy carbon electrode surface by multiple adenine bases deriving from CoA and acting as the side groups along the polymeric backbone, which displays efficient H2O2-electrocatalyzing activity. More importantly, by using the formed polymer as signal output, the process is implemented to quantitatively analyze the activity of CS. Under the optimal conditions, CS with a detection limit as low as 0.00165 U/mu L could be sensitively probed with a wide linear range from 0.0033 to 0.264 U/mu L. Furthermore, with the character of label-free detection, high sensitivity and excellent selectivity, this strategy offers a convenient and specific method for CS activity detection and relevant inhibitors screening, which holds a promising potential in the practical application of CS-based biochemical research, disease diagnosis and drug discovery. (C) 2016 Elsevier B.V. All rights reserved.
机译:我们在这里报告了基于对辅酶A(CoA)-Ag(I)重复单元形成的核酸模拟配位聚合物(CP)进行详细研究的无标记和灵敏的电化学方法,用于探测柠檬酸合酶(CS)活性。我们的生物传感方法提供了一种特殊而重要的检测机制:CS可以催化乙酰辅酶A(Ac-CoA)与草酰乙酸(OAA)之间的必不可少的缩合反应,从而形成柠檬酸和CoA。然后,在存在Ag(I)的情况下,由于CoA的巯基对Ag(I)的强络合能力,可以原位形成CoA-Ag(I)CP。生成的CoA-Ag(I)CP通过多个CoA衍生的腺嘌呤碱基附着在石墨烯修饰的玻碳电极表面,并沿聚合物主链充当侧基,表现出有效的H2O2电催化活性。更重要的是,通过使用形成的聚合物作为信号输出,可以实施该过程以定量分析CS的活性。在最佳条件下,可以灵敏地检测到检测限低至0.00165 U /μL的CS,线性范围从0.0033至0.264 U /μL。此外,具有无标记检测,高灵敏度和高灵敏度的特点。该策略具有极好的选择性,为CS活性检测和相关抑制剂的筛选提供了一种方便且特定的方法,在基于CS的生化研究,疾病诊断和药物发现的实际应用中具有广阔的前景。 (C)2016 Elsevier B.V.保留所有权利。

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