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等离子体纳米结构增强的拉曼散射用于检测 SARS-CoV-2 核衣壳蛋白和刺突蛋白变体。

Plasmonic nanostructure-enhanced Raman scattering for detection of SARS-CoV-2 nucleocapsid protein and spike protein variants.

机构信息

Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei, 10607, Taiwan; Department of Chemical Engineering, National Taiwan University, Taipei, 10617, Taiwan.

Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei, 10607, Taiwan; Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei, 10617, Taiwan.

出版信息

Anal Chim Acta. 2023 Jan 25;1239:340651. doi: 10.1016/j.aca.2022.340651. Epub 2022 Nov 21.

DOI:10.1016/j.aca.2022.340651
PMID:36628748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9677586/
Abstract

Epidemiological control and public health monitoring during the outbreaks of infectious viral diseases rely on the ability to detect viral pathogens. Here we demonstrate a rapid, sensitive, and selective nanotechnology-enhanced severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection based on the surface-enhanced Raman scattering (SERS) responses from the plasma-engineered, variant-specific antibody-functionalized silver microplasma-engineered nanoassemblies (AgMEN) interacting with the SARS-CoV-2 spike (S) and nucleocapsid (N) proteins. The three-dimensional (3D) porous AgMEN with plasmonic-active nanostructures provide a high sensitivity to virus detection via the remarkable SERS signal collection. Moreover, the variant-specific antibody-functionalization on the SERS-active AgMEN enabled the high selectivity of the SARS-CoV-2 S variants, including wild-type, Alpha, Delta, and Omicron, under the simulated human saliva conditions. The exceptional ultrahigh sensitivity of our SERS biosensor was demonstrated via SARS-CoV-2 S and N proteins at the detection limit of 1 fg mL and 0.1 pg mL, respectively. Our work demonstrates a versatile SERS-based detection platform can be applied for the ultrasensitive detection of virus variants, infectious diseases, and cancer biomarkers.

摘要

在传染病爆发期间,流行病学控制和公共卫生监测依赖于检测病毒病原体的能力。在这里,我们展示了一种基于等离子体工程化、具有变体特异性的抗体功能化银微等离子体工程纳米组装体(AgMEN)与 SARS-CoV-2 刺突(S)和核衣壳(N)蛋白相互作用的表面增强拉曼散射(SERS)响应的快速、灵敏和选择性 SARS-CoV-2 检测的纳米技术增强方法。具有等离子体活性纳米结构的三维(3D)多孔 AgMEN 通过显著的 SERS 信号收集提供了对病毒检测的高灵敏度。此外,SERS 活性 AgMEN 上的变体特异性抗体功能化使得在模拟人类唾液条件下对 SARS-CoV-2 S 变体(包括野生型、Alpha、Delta 和 Omicron)具有高选择性。我们的 SERS 生物传感器通过 SARS-CoV-2 S 和 N 蛋白的检测限分别达到 1 fg mL 和 0.1 pg mL,证明了其卓越的超高灵敏度。我们的工作展示了一种多功能的基于 SERS 的检测平台,可用于超灵敏检测病毒变体、传染病和癌症生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/f2c38b92da14/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/de93fdba494b/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/9a6ab8c90072/sc1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/07ac125627b3/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/a04514b05e2f/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/83cbe0d797c9/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/7c7c8d3f12e1/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/f2c38b92da14/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/de93fdba494b/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/9a6ab8c90072/sc1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/07ac125627b3/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/a04514b05e2f/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/83cbe0d797c9/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/7c7c8d3f12e1/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5994/9677586/f2c38b92da14/gr5_lrg.jpg

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