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基于多肽引发金纳米粒子组装的比色和电化学方法用于检测 SARS-CoV-2 主蛋白酶。

Colorimetric and Electrochemical Methods for the Detection of SARS-CoV-2 Main Protease by Peptide-Triggered Assembly of Gold Nanoparticles.

机构信息

College of Chemistry and Chemical Engineering, Pingdingshan University, Pingdingshan 467000, China.

Henan Province of Key Laboratory of New Optoelectronic Functional Materials, College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, China.

出版信息

Molecules. 2022 Jan 18;27(3):615. doi: 10.3390/molecules27030615.

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (Mpro) has been regarded as one of the ideal targets for the development of antiviral drugs. The currently used methods for the probing of Mpro activity and the screening of its inhibitors require the use of a double-labeled peptide substrate. In this work, we suggested that the label-free peptide substrate could induce the aggregation of AuNPs through the electrostatic interactions, and the cleavage of the peptide by the Mpro inhibited the aggregation of AuNPs. This fact allowed for the visual analysis of Mpro activity by observing the color change of the AuNPs suspension. Furthermore, the co-assembly of AuNPs and peptide was achieved on the peptide-covered electrode surface. Cleavage of the peptide substrate by the Mpro limited the formation of AuNPs/peptide assembles, thus allowing for the development of a simple and sensitive electrochemical method for Mpro detection in serum samples. The change of the electrochemical signal was easily monitored by electrochemical impedance spectroscopy (EIS). The detection limits of the colorimetric and electrochemical methods are 10 and 0.1 pM, respectively. This work should be valuable for the development of effective antiviral drugs and the design of novel optical and electrical biosensors.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)主要蛋白酶(Mpro)已被认为是开发抗病毒药物的理想靶点之一。目前用于探测 Mpro 活性和筛选其抑制剂的方法需要使用双标记肽底物。在这项工作中,我们提出无标记肽底物可以通过静电相互作用诱导 AuNPs 的聚集,并且 Mpro 对肽的切割抑制了 AuNPs 的聚集。这一事实允许通过观察 AuNPs 悬浮液的颜色变化来进行 Mpro 活性的可视化分析。此外,AuNPs 和肽的共组装在肽覆盖的电极表面上实现。Mpro 对肽底物的切割限制了 AuNPs/肽组装的形成,从而开发出一种简单灵敏的电化学方法,用于检测血清样品中的 Mpro。电化学阻抗谱(EIS)可轻松监测电化学信号的变化。比色法和电化学方法的检测限分别为 10 和 0.1 pM。这项工作对于开发有效的抗病毒药物和设计新型光学和电气生物传感器应该具有重要价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd8b/8840628/3cb26c4476ac/molecules-27-00615-sch001.jpg

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