Department of Forensic Science, Environmental and Life Sciences Program, Trent University, Ontario, Canada, K9L0G2.
Nicoya Lifesciences Inc., Kitchener, Ontario, Canada, N2G2K4.
Analyst. 2021 Nov 22;146(23):7207-7217. doi: 10.1039/d1an01458g.
In this work, we designed and developed a method to detect S1 spike protein of SARS-CoV-2. The portable Localized Surface Plasmon Resonance instrument equipped with a two-channel system was combined with the biotin-streptavidin platform on a nanogold surface to immobilize biotinylated aptamers. The proposed assay does not utilize antibodies or enzyme-based reagents, further simplifying the detection method. Using aptamer-protein bioaffinity interactions, the aptasensor selectively and specifically detected in real-time S1 spike protein, rather than S2 spike protein, RBD spike protein, or bovine serum albumin. The dynamic range and limit of detection of the aptasensor was determined to be 1 nM-100 nM and 0.26 nM, respectively. Notably, aptasensor detected preferentially S1 protein of SARS-CoV-2 compared to SARS-CoV and detected S1 protein with >95% recovery in artificial saliva, and serum albumin, excellent repeatability and shelf-life stability. The method may provide a low-cost, rapid, and real-time detection and monitoring of viruses in the general public.
在这项工作中,我们设计并开发了一种用于检测 SARS-CoV-2 S1 刺突蛋白的方法。该便携式局部表面等离子体共振仪器配备双通道系统,结合纳米金表面上的生物素-链霉亲和素平台,将生物素化适体固定化。该检测方法不使用抗体或基于酶的试剂,进一步简化了检测方法。该适体传感器利用适体-蛋白生物亲和力相互作用,实时选择性和特异性地检测 S1 刺突蛋白,而不是 S2 刺突蛋白、RBD 刺突蛋白或牛血清白蛋白。该适体传感器的动态范围和检测限分别确定为 1 nM-100 nM 和 0.26 nM。值得注意的是,与 SARS-CoV 相比,适体传感器更优先地检测 SARS-CoV-2 的 S1 蛋白,并且在人工唾液和血清白蛋白中,S1 蛋白的检测回收率>95%,具有极好的重复性和货架期稳定性。该方法可用于为公众提供低成本、快速和实时的病毒检测和监测。