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基于碳纳米纤维纳米电极阵列增强交流伏安法的电化学蛋白酶生物传感器

Electrochemical Protease Biosensor Based on Enhanced AC Voltammetry Using Carbon Nanofiber Nanoelectrode Arrays.

作者信息

Swisher Luxi Z, Syed Lateef U, Prior Allan M, Madiyar Foram R, Carlson Kyle R, Nguyen Thu A, Hua Duy H, Li Jun

机构信息

Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.

出版信息

J Phys Chem C Nanomater Interfaces. 2013 Feb 28;117(8):4268-4277. doi: 10.1021/jp312031u.

Abstract

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 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 as (4.3 ± 0.8) × 10 Ms for cathepsin B and (1.13 ± 0.38) × 10 Ms for legumain. This method could be developed as portable multiplex electronic techniques for rapid cancer diagnosis and treatment monitoring.

摘要

我们报道了一种使用由垂直排列的碳纳米纤维(VACNFs)制成的纳米电极阵列(NEAs)来测量蛋白酶活性的电化学方法。直径约150 nm、长度为3至5μm的VACNFs生长在导电基底上,并封装在SiO基质中。经过抛光和等离子体蚀刻后,可控的VACNF尖端暴露出来,形成嵌入式VACNF NEA。两种对癌症介导的蛋白酶豆荚蛋白酶和组织蛋白酶B具有特异性的四肽共价连接到暴露的VACNF尖端,在远端连接有二茂铁(Fc)部分。Fc的氧化还原信号可以通过交流伏安法(ACV)在约1 kHz频率下在VACNF NEAs上进行测量,由于VACNF独特的内部结构,其显示出与宏观玻碳电极不同的特性。增强的ACV特性能够对蛋白酶对表面附着的四肽的蛋白水解切割进行动力学测量,并通过荧光测定进一步验证。数据可以用非均相米氏模型进行分析,组织蛋白酶B的“特异性常数”/K为(4.3±0.8)×10 M·s,豆荚蛋白酶为(1.13±0.38)×10 M·s。该方法可发展成为用于快速癌症诊断和治疗监测的便携式多重电子技术。

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