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基于适配体功能化金纳米粒子的 SARS-CoV-2 检测

SARS-CoV-2 detection with aptamer-functionalized gold nanoparticles.

机构信息

Department of Mechanical Engineering, McMaster University, Hamilton, Ontario, Canada.

School of Biomedical Engineering, McMaster University, Hamilton, Ontario, Canada.

出版信息

Talanta. 2022 Jan 1;236:122841. doi: 10.1016/j.talanta.2021.122841. Epub 2021 Sep 1.

Abstract

A rapid detection test for SARS-CoV-2 is urgently required to monitor virus spread and containment. Here, we describe a test that uses nanoprobes, which are gold nanoparticles functionalized with an aptamer specific to the spike membrane protein of SARS-CoV-2. An enzyme-linked immunosorbent assay confirms aptamer binding with the spike protein on gold surfaces. Protein recognition occurs by adding a coagulant, where nanoprobes with no bound protein agglomerate while those with sufficient bound protein do not. Using plasmon absorbance spectra, the nanoprobes detect 16 nM and higher concentrations of spike protein in phosphate-buffered saline. The time-varying light absorbance is examined at 540 nm to determine the critical coagulant concentration required to agglomerates the nanoprobes, which depends on the protein concentration. This approach detects 3540 genome copies/μl of inactivated SARS-CoV-2.

摘要

快速检测 SARS-CoV-2 病毒是监测病毒传播和控制的迫切需要。在这里,我们描述了一种使用纳米探针的检测方法,该探针是用针对 SARS-CoV-2 刺突膜蛋白的适体功能化的金纳米粒子。酶联免疫吸附试验证实了适体与金表面上的刺突蛋白的结合。通过添加凝结剂来实现蛋白质识别,没有结合蛋白的纳米探针聚集,而具有足够结合蛋白的纳米探针则不聚集。使用等离子体吸收光谱,纳米探针在磷酸盐缓冲液中检测到 16 nM 及更高浓度的刺突蛋白。通过检测 540nm 处随时间变化的光吸收来确定使纳米探针聚集所需的临界凝结剂浓度,该浓度取决于蛋白质浓度。该方法可检测到 3540 基因组拷贝/μl 的灭活 SARS-CoV-2。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8519/8409056/599e2f553f66/ga1_lrg.jpg

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