Functional and Evolutionary Entomology-Gembloux Agro-Bio Tech, University of Liège, 5030 Gembloux, Belgium.
ACS Nano. 2022 Apr 26;16(4):6165-6175. doi: 10.1021/acsnano.1c11643. Epub 2022 Apr 4.
We report the peptide-programmed fractal assembly of silver nanoparticles (AgNPs) in a diffusion-limited aggregation (DLA) mode, and this change in morphology generates a significant color change. We show that peptides with specific repetitions of defined amino acids (.., arginine, histidine, or phenylalanine) can induce assembly and coalescence of the AgNPs (20 nm) into a hyperbranched structure (AgFSs) (∼2 μm). The dynamic process of this assembly was systematically investigated, and the extinction of the nanostructures can be modulated from 400 to 600 nm by varying the peptide sequences and molar ratio. According to this rationale, two strategies of SARS-CoV-2 detection were investigated. The activity of the main protease (Mpro) involved in SARS-CoV-2 was validated with a peptide substrate that can bridge the AgNPs after the proteolytic cleavage. A sub-nanomolar limit of detection (0.5 nM) and the capacity to distinguish by the naked eye in a wide concentration range (1.25-30 nM) were achieved. Next, a multichannel sensor-array based on multiplex peptides that can visually distinguish SARS-CoV-2 proteases from influenza proteases in doped human samples was investigated.
我们报告了银纳米粒子(AgNPs)在扩散限制聚集(DLA)模式下的肽程序化分形组装,这种形态变化产生了显著的颜色变化。我们表明,具有特定重复定义氨基酸(...,精氨酸、组氨酸或苯丙氨酸)的肽可以诱导 AgNPs(20nm)组装和聚合并形成支化结构(AgFSs)(∼2μm)。我们系统地研究了这个组装的动态过程,通过改变肽序列和摩尔比,可以将纳米结构的消光从 400nm 调节到 600nm。根据这一原理,我们研究了两种 SARS-CoV-2 检测策略。用肽底物验证了 SARS-CoV-2 中涉及的主要蛋白酶(Mpro)的活性,该肽底物在蛋白酶切割后可以桥接 AgNPs。实现了纳摩尔级别的检测限(0.5 nM),并且能够在较宽的浓度范围内(1.25-30 nM)用肉眼区分。接下来,我们研究了一种基于多通道传感器阵列的方法,该方法使用的多肽可以在掺杂的人体样本中视觉区分 SARS-CoV-2 蛋白酶和流感蛋白酶。