Department of NanoEngineering, University of California, San Diego, La Jolla, California 92093, United States.
Institute of Materials Research and Engineering, Agency for Science, Technology and Research, Singapore 138634.
Nano Lett. 2022 Nov 23;22(22):8932-8940. doi: 10.1021/acs.nanolett.2c03052. Epub 2022 Nov 8.
Plasmonic coupling nanoparticle assembly is a popular signal-generation method in bioanalytical sensors. Here, we customized an all-peptide-based ligand that carries an anchoring group, polyproline spacer, biomolecular recognition, and zwitterionic domains for functionalizing gold nanoparticles (AuNPs) as a colorimetric enzyme sensor. Our results underscore the importance of the polyproline module, which enables the SARS-CoV-2 main protease (M) to recognize the peptidic ligand on nanosurfaces for subsequent plasmonic coupling Coulombic interactions. AuNP aggregation is favored by the lowered surface potential due to enzymatic unveiling of the zwitterionic module. Therefore, this system provides a naked-eye measure for M. No proteolysis occurs on AuNPs modified with a control ligand lacking a spacer domain. Overall, this all-peptide-based ligand does not require complex molecular conjugations and hence offers a simple and promising route for plasmonic sensing other proteases.
等离子体耦合纳米粒子组装是生物分析传感器中一种常用的信号产生方法。在这里,我们定制了一种基于全肽的配体,该配体带有一个锚固基团、一个脯氨酸间隔物、生物分子识别和两性离子结构域,用于功能化金纳米粒子(AuNPs)作为比色酶传感器。我们的结果强调了聚脯氨酸模块的重要性,该模块使 SARS-CoV-2 主要蛋白酶(M)能够识别纳米表面上的肽配体,以进行后续的等离子体耦合库仑相互作用。由于两性离子模块的酶促揭示,AuNP 聚集更有利于降低表面势能。因此,该系统为 M 提供了一种肉眼可见的测量方法。在没有间隔物域的对照配体修饰的 AuNPs 上不会发生蛋白水解。总的来说,这种基于全肽的配体不需要复杂的分子偶联,因此为等离子体感应其他蛋白酶提供了一种简单而有前途的途径。