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Electrochemical protease biosensor based on enhanced AC voltammetry using carbon nanofiber nanoelectrode arrays

机译:基于碳纳米纤维纳米电极阵列基于增强交流伏安法的电化学蛋白酶生物传感器

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摘要

We report an electrochemical method for measuring the activity of proteases using nanoelectrode arrays (NEAs) fabricated with vertically aligned carbon nanofibers (VACNFs). The VACNFs of ~150 nm in diameter and 3 to 5 μm in length were grown on conductive substrates and encapsulated in SiO[subscript 2] matrix. After polishing and plasma etching, controlled VACNF tips are exposed to form an embedded VACNF NEA. Two types of tetrapeptides specific to cancer-mediated proteases legumain and cathepsin B are covalently attached to the exposed VACNF tip, with a ferrocene (Fc) moiety linked at the distal end. The redox signal of Fc can be measured with AC voltammetry (ACV) at ~1 kHz frequency on VACNF NEAs, showing distinct properties from macroscopic glassy carbon electrodes due to VACNF’s unique interior structure. The enhanced ACV properties enable the kinetic measurements of proteolytic cleavage of the surface-attached tetrapeptides by proteases, further validated with a fluorescence assay. The data can be analyzed with a heterogeneous Michaelis-Menten model, giving “specificity constant” k[subscript cat]/K[subscript m] as (4.3 ± 0.8) x 10[superscript 4] Mˉ¹sˉ¹ for cathepsin B and (1.13 ± 0.38) x 10[superscript 4] Mˉ¹sˉ¹ for legumain. This method could be developed as portable multiplex electronic techniques for rapid cancer diagnosis and treatment monitoring.
机译:我们报告了一种电化学方法,该方法使用垂直排列的碳纳米纤维(VACNFs)制造的纳米电极阵列(NEA)测量蛋白酶的活性。在导电基板上生长直径约为150 nm,长度为3至5μm的VACNF,并将其封装在SiO [下标2]基质中。抛光和等离子蚀刻后,将受控的VACNF尖端暴露以形成嵌入式VACNF NEA。癌症介导的蛋白酶legumain和组织蛋白酶B特异的两种四肽共价连接到暴露的VACNF末端,二茂铁(Fc)部分连接在末端。 Fc的氧化还原信号可以在VACNF NEA上以AC伏安法(ACV)在约1 kHz的频率下进行测量,由于VACNF独特的内部结构,它具有与宏观玻璃碳电极不同的特性。增强的ACV特性使得能够通过蛋白酶对表面附着的四肽进行蛋白水解切割的动力学测量,并通过荧光分析进一步验证。可以使用异构Michaelis-Menten模型分析数据,对于组织蛋白酶B,“特异常数” k [下标cat] / K [下标m]为(4.3±0.8)x 10 [上标4]Mˉsˉ¹,而(1.13±0.38) )×10 6上豆蔻因的M -1 s 1。该方法可以开发为便携式多路电子技术,用于快速癌症诊断和治疗监测。

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