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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 >Quantitative electrochemical detection of cathepsin B activity in complex tissue lysates using enhanced AC voltammetry at carbon nanofiber nanoelectrode arrays
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Quantitative electrochemical detection of cathepsin B activity in complex tissue lysates using enhanced AC voltammetry at carbon nanofiber nanoelectrode arrays

机译:使用增强的交流伏安法在碳纳米纤维纳米电极阵列上定量电化学检测复杂组织裂解物中的组织蛋白酶B活性

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摘要

The proteolytic activity of a cancer-related enzyme cathepsin B is measured with alternating current voltammetry (ACV) using ferrocene (Fc) labeled tetrapeptides attached to nanoelectrode arrays (NEAs) fabricated with vertically aligned carbon nanofibers (VACNFs). This combination enables the use of high AC frequencies (?1 kHz) with enhanced electrochemical signals. The specific proteolysis of the Fc- peptide by cathepsin B produces decay in the ACV peak current versus the reaction time. The exponential component of the raw data can be extracted and defined as the "extracted proteolytic signal" which allows consistent quantitative analyses using a heterogeneous Michaelis-Menten model. A "specificity constant" k_(cat)/K_M=(3,68 ± 0.50) x 10~4 M~(-1)s~(-1) for purified cathepsin B was obtained. The detections of cathepsin B activity in different concentrations of whole lysate of human breast tissue, tissue lysate spiked with varied concentrations of cathepsin B,and the tissue lysate after immunoprecipitation showed that there is ?13.4 nM higher cathepsin B concentration in 29.1 μg mL~(-1) of whole tissue lysate than the immunop recip itated sample. The well-defined regular VACNF NEAs by e-beam lithography show a much faster kinetics for cathepsin B proteolysis with k_(cat)/K_M=9.2 x 10~4 M~(-1)s~(-1). These results illustrate the potential of this technique as a portable multiplex electronic system for cancer diagnosis by rapid protease profiling of serum or blood samples.
机译:癌症相关的组织蛋白酶B的蛋白水解活性是通过交流伏安法(ACV)使用二茂铁(Fc)标记的四肽连接到用垂直排列的碳纳米纤维(VACNFs)制成的纳米电极阵列(NEA)来测量的。这种结合使得能够使用具有增强的电化学信号的高AC频率(?1 kHz)。组织蛋白酶B对Fc肽的特异性蛋白水解作用导致ACV峰值电流相对于反应时间的衰减。可以提取原始数据的指数成分并将其定义为“提取的蛋白水解信号”,从而可以使用异构Michaelis-Menten模型进行一致的定量分析。对于纯化的组织蛋白酶B,获得“特异性常数” k_(cat)/ K_M =(3,68±0.50)×10〜4 M〜(-1)s〜(-1)。在不同浓度的人乳腺组织全裂解液,组织裂解液中掺入不同浓度的组织蛋白酶B以及免疫沉淀后的组织裂解液中,组织蛋白酶B活性的检测结果表明,在29.1μgmL〜中,组织蛋白酶B的浓度高出约13.4 nM。 -1)整个组织的裂解物要比免疫沉淀的样品多。通过电子束光刻,清晰定义的常规VACNF NEA显示出组织蛋白酶B蛋白水解的动力学快得多,k_(cat)/K_M=9.2 x 10〜4 M〜(-1)s〜(-1)。这些结果说明了该技术作为通过血清或血液样品的快速蛋白酶谱分析进行癌症诊断的便携式多重电子系统的潜力。

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