适体
表面等离子共振
链霉亲和素
生物素化
牛血清白蛋白
检出限
化学
靶蛋白
色谱法
生物物理学
纳米颗粒
生物素
材料科学
纳米技术
分子生物学
生物化学
生物
基因
作者
Tyra Lewis,Erin Giroux,Marko Jović,Sanela Martić
出处
期刊:Analyst
[The Royal Society of Chemistry]
日期:2021-01-01
卷期号:146 (23): 7207-7217
被引量:29
摘要
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.
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