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基于纳米颗粒的一锅式比色和电化学蛋白酶检测中具有封端和切割位点基序的双功能肽

Dual-Role Peptide with Capping and Cleavage Site Motifs in Nanoparticle-Based One-Pot Colorimetric and Electrochemical Protease Assay.

作者信息

Szabó Tamás, Bakos István, Vrbovszki Barbara, Jeerapan Itthipon, Pekker Péter, Mihály Judith, Németh Krisztina, Wang Joseph, Keresztes Zsófia

机构信息

Research Centre for Natural Sciences, Magyar tudósok körútja 2., 1117 Budapest, Hungary.

Laboratory of Nano-Bioelectronics, Department of Nanoengineering, Jacobs School of Engineering, University of California San Diego, La Jolla, California 92093, United States.

出版信息

ACS Omega. 2023 Jun 9;8(25):22556-22566. doi: 10.1021/acsomega.3c00771. eCollection 2023 Jun 27.

Abstract

A new method for enzyme substrate assembly and its use in proteolytic enzyme assays with colorimetric and electrochemical detection is presented. The novelty of the method is the use of dual-function synthetic peptide containing both gold clustering and protease-sensitive moieties, which not only induces the simple formation of the peptide-decorated gold nanoparticle test substrates but also allows for the detection of proteolysis in the same batch. Protease-treated nanoparticles with a destabilized peptide shell became more prone to electroactivity, and thus, the model enzyme plasmin activity could be quantified with stripping square wave voltammetry analysis as well, giving an alternative method to conduct aggregation-based assays. Spectrophotometric and electrochemical calibration data proved to be linear within the 40-100 nM active enzyme concentration range, with possible extensions of the dynamic range by varying substrate concentration. The simple initial components and the ease of synthesis make the assay substrate preparation economic and easy to implement. The possibility of cross-check analytical results with two independent measurement techniques in the same batch greatly increases the applicability of the proposed system.

摘要

本文介绍了一种酶底物组装的新方法及其在比色和电化学检测的蛋白水解酶测定中的应用。该方法的新颖之处在于使用了同时含有金簇和蛋白酶敏感部分的双功能合成肽,它不仅能诱导形成肽修饰的金纳米颗粒测试底物,还能在同一批次中检测蛋白水解。经蛋白酶处理后肽壳不稳定的纳米颗粒更易于产生电活性,因此,模型酶纤溶酶的活性也可用溶出方波伏安法进行定量分析,从而提供了一种进行基于聚集的测定的替代方法。分光光度法和电化学校准数据在40-100 nM活性酶浓度范围内呈线性,通过改变底物浓度可扩展动态范围。简单的初始成分和易于合成使得测定底物的制备经济且易于实施。在同一批次中用两种独立测量技术交叉核对分析结果的可能性大大提高了所提出系统的适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b8a/10308550/790580890e6b/ao3c00771_0008.jpg

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