Department of Chemistry, Capital Normal University, Beijing 100048, China.
Anal Chem. 2022 Nov 22;94(46):16231-16236. doi: 10.1021/acs.analchem.2c03949. Epub 2022 Nov 11.
The accurate detection of trace protein biomarkers is critical for disease diagnosis, healthcare, and pathology research. Currently, the main predicaments of techniques are low sensitivity, prolonged procedures, and the need for specialized devices. Moreover, multistep handling and nonspecific biofouling can lead to high background noise and false positives. To overcome these barriers, a novel ultrasensitive electrochemical platform was developed by combining an electrochemistry approach with the silver mirror reaction to detect proteins at the zeptomolar level. This assay can be accomplished in about only 18 min. As a proof of the concept, human immunoglobulin G (h-IgG) as a model analyte exhibited an ultralow detection limit of 6.31 ag mL (0.04 zeptomoles mL). This strategy can be exploited as a universal approach for the ultrasensitive detection of various proteins in clinical diagnostics and point-of-care testing.
痕量蛋白质生物标志物的准确检测对疾病诊断、医疗保健和病理学研究至关重要。目前,技术主要面临灵敏度低、过程冗长以及需要专用设备等困境。此外,多步处理和非特异性生物污垢会导致背景噪声高和假阳性。为了克服这些障碍,通过将电化学方法与银镜反应相结合,开发了一种新型超灵敏电化学平台,可在皮摩尔水平检测蛋白质。该测定法可在大约 18 分钟内完成。作为概念验证,以人免疫球蛋白 G(h-IgG)作为模型分析物,检测限低至 6.31 ag mL(0.04 皮摩尔 mL)。该策略可作为在临床诊断和即时检测中用于超灵敏检测各种蛋白质的通用方法。