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基于纳米机械传感器平台的 SARS-CoV-2 高灵敏度和超快速抗原检测。

Highly sensitive and ultra-rapid antigen-based detection of SARS-CoV-2 using nanomechanical sensor platform.

机构信息

Department of Material Science and Engineering and NUANCE Center, Northwestern University, Evanston, IL, 60208, USA.

Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.

出版信息

Biosens Bioelectron. 2022 Jan 1;195:113647. doi: 10.1016/j.bios.2021.113647. Epub 2021 Sep 17.

DOI:10.1016/j.bios.2021.113647
PMID:34583103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8445766/
Abstract

The rapid spread of COVID-19 including recent emergence of new variants with its extreme range of pathologies create an urgent need to develop a versatile sensor for a rapid, precise, and highly sensitive detection of SARS-CoV-2. Herein, we report a microcantilever-based optical detection of SARS-CoV-2 antigenic proteins in just few minutes with high specificity by employing fluidic-atomic force microscopy (f-AFM) mediated nanomechanical deflection method. The corresponding antibodies against the target antigens were first grafted on the gold-coated microcantilever surface pre-functionalized with EDC-NHS chemistry for a suitable antibody-antigen interaction. Rapid detection of SARS-CoV-2 nucleocapsid (N) and spike (S1) receptor binding domain (RBD) proteins was first demonstrated at a clinically relevant concentration down to 1 ng/mL (33 pM) by real-time monitoring of nanomechanical signal induced by antibody-antigen interaction. More importantly, we further show high specific detection of antigens with nasopharyngeal swab specimens from patients pre-determined with qRT-PCR. The results take less than 5 min (swab to signal ≤5 min) and exhibit high selectivity and analytical sensitivity (LoD: 100 copies/ ml; 0.71 ng/ml of N protein). These findings demonstrate potential for nanomechanical signal transduction towards rapid antigen detection for early screening of SARS-CoV-2 and its related mutants.

摘要

包括最近出现的具有极端病理范围的新变体在内的 COVID-19 的迅速传播,迫切需要开发一种多功能传感器,以快速、精确和高度灵敏地检测 SARS-CoV-2。在此,我们报告了一种基于微悬臂梁的光学检测方法,该方法利用流体原子力显微镜(f-AFM)介导的纳米机械挠度方法,在短短几分钟内即可实现 SARS-CoV-2 抗原蛋白的高特异性检测。首先,将针对靶抗原的相应抗体通过 EDC-NHS 化学预功能化的金涂覆微悬臂梁表面接枝,以实现合适的抗体-抗原相互作用。通过实时监测抗体-抗原相互作用引起的纳米机械信号,首次在临床相关浓度下(低至 1ng/mL(33pM))证明了对 SARS-CoV-2 核衣壳(N)和刺突(S1)受体结合域(RBD)蛋白的快速检测。更重要的是,我们进一步展示了对通过 qRT-PCR 预先确定的患者鼻咽拭子标本中抗原的高特异性检测。结果耗时不到 5 分钟(从拭子到信号的时间≤5 分钟),并表现出高选择性和分析灵敏度(LoD:100 拷贝/ml;N 蛋白的 0.71ng/ml)。这些发现证明了纳米机械信号转导在快速抗原检测中的潜力,可用于 SARS-CoV-2 及其相关突变体的早期筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1858/8445766/df9fc1e97d62/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1858/8445766/714540182894/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1858/8445766/95e9aec7838c/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1858/8445766/9d9c36d57de2/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1858/8445766/3cd93517f627/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1858/8445766/df9fc1e97d62/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1858/8445766/714540182894/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1858/8445766/95e9aec7838c/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1858/8445766/9d9c36d57de2/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1858/8445766/3cd93517f627/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1858/8445766/df9fc1e97d62/gr5_lrg.jpg

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