Centre for Molecular Nanometrology, Technology and Innovation Centre, University of Strathclyde, 99 George Street, Glasgow, UK.
Analyst. 2017 Jun 26;142(13):2484-2490. doi: 10.1039/c7an00887b.
Artificial enzymes have become an increasingly interesting area of research due to their many advantages over natural protein enzymes which are expensive, difficult to isolate and unable to stand harsh environments. An important area of this research involves using metal nanoparticles as artificial enzymes, known as nanozymes, which exhibit peroxidase-like activity enabling them to catalyse the oxidation of substrates such as 3,3',5,5'-tetramethylbenzidine (TMB) in the presence of hydrogen peroxide (HO), giving a colorimetric response. Here we exploit the catalytic activity of silver nanoparticles (Ag NPs) in a surface based silver-linked immunosorbent assay (SLISA) to detect human C-reactive protein (CRP), an inflammatory marker. Ag NPs were conjugated to antibodies with specific recognition for the corresponding target antigenic molecule, CRP, and the Ag NPs were used to catalyse the oxidation of TMB by HO. The resulting coloured oxidation product was detected using SERRS. We demonstrate that Ag NPs can replace the enzymes used in a conventional ELISA and a detection limit of 1.09 ng mL of CRP can be achieved. It indicates the promise for SLISAs for biomarker detection and opens the way for further assays of this nature to be created. This novel assay has the potential to be optimised to detect lower levels of CRP and can be further extended for the sensitive and specific detection of other relevant biomarkers.
由于人工酶相对于天然蛋白质酶具有许多优势,例如成本高、难以分离以及无法耐受恶劣环境,因此人工酶已成为一个日益引人关注的研究领域。该研究的一个重要领域涉及使用金属纳米粒子作为人工酶,即纳米酶,其具有过氧化物酶样活性,能够在过氧化氢 (HO) 的存在下催化底物(如 3,3',5,5'-四甲基联苯胺 (TMB))的氧化,产生比色响应。在这里,我们利用银纳米粒子 (Ag NPs) 的催化活性在基于表面的银连接免疫吸附测定 (SLISA) 中检测人 C 反应蛋白 (CRP),这是一种炎症标志物。Ag NPs 与针对相应靶抗原分子 CRP 的特异性抗体结合,并用于 HO 催化 TMB 的氧化。使用 SERRS 检测到生成的有色氧化产物。我们证明 Ag NPs 可以替代常规 ELISA 中的酶,并且可以达到 1.09ng mL CRP 的检测限。这表明 SLISAs 有望用于生物标志物检测,并为进一步开发此类检测方法开辟了道路。这种新型检测方法有可能被优化以检测更低水平的 CRP,并且可以进一步扩展用于其他相关生物标志物的灵敏和特异性检测。