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Label-free electrochemical impedance detection of kinase and phosphatase activities using carbon nanofiber nanoelectrode arrays

机译:使用碳纳米纤维纳米电极阵列的激酶和磷酸酶活性的无标记电化学阻抗检测

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摘要

We demonstrate the feasibility of a label-free electrochemical method to detect the kinetics of phosphorylation and dephosphorylation of surface-attached peptides catalyzed by kinase and phosphatase, respectively. The peptides with a sequence specific to c-Src tyrosine kinase and protein tyrosine phosphatase 1B (PTP1B) were first validated with ELISA-based protein tyrosine kinase assay and then functionalized on vertically aligned carbon nanofiber (VACNF) nanoelectrode arrays (NEAs). Real-time electrochemical impedance spectroscopy (REIS) measurements showed reversible impedance changes upon the addition of c-Src kinase and PTP1B phosphatase. Only a small and unreliable impedance variation was observed during the peptide phosphorylation, but a large and fast impedance decrease was observed during the peptide dephosphorylation at different PTP1B concentrations. The REIS data of dephosphorylation displayed a well-defined exponential decay following the Michaelis-Menten heterogeneous enzymatic model with a specific constant, kcat/Km, of (2.1 ± 0.1) × 107 M−1 s−1. Consistent values of the specific constant was measured at PTP1B concentration varying from 1.2 to 2.4 nM with the corresponding electrochemical signal decay constant varying from 38.5 to 19.1 s. This electrochemical method can be potentially used as a label-free method for profiling enzyme activities in fast reactions.
机译:我们证明了无标记的电化学方法检测分别由激酶和磷酸酶催化的表面附着肽的磷酸化和去磷酸化动力学的可行性。首先使用基于ELISA的蛋白质酪氨酸激酶测定法验证具有c-Src酪氨酸激酶和蛋白质酪氨酸磷酸酶1B(PTP1B)特异性序列的肽,然后在垂直排列的碳纳米纤维(VACNF)纳米电极阵列(NEA)上进行功能化。实时电化学阻抗谱(REIS)测量显示,添加c-Src激酶和PTP1B磷酸酶后可逆的阻抗变化。在肽磷酸化过程中,仅观察到很小且不可靠的阻抗变化,但在不同PTP1B浓度的肽脱磷酸过程中观察到了大而快速的阻抗下降。遵循Michaelis-Menten异质酶模型,去磷酸化的REIS数据显示出明确定义的指数衰减,其特定常数kcat / Km为(2.1±0.1)×10 7 M - 1 s -1 。在PTP1B浓度从1.2到2.4 nM范围内测量比常数的一致值,相应的电化学信号衰减常数在38.5到19.1 s之间变化。该电化学方法可以潜在地用作无标记方法,用于分析快速反应中的酶活性。

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