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利用单颗粒电感耦合等离子体质谱法同时检测 SARS-CoV-2 和甲型流感(H3N2)的均相核酸检测方法。

A homogeneous nucleic acid assay for simultaneous detection of SARS-CoV-2 and influenza A (H3N2) by single-particle inductively coupled plasma mass spectrometry.

机构信息

Department of Chemistry, Wuhan University, Wuhan, 430072, China.

Department of Chemistry, Wuhan University, Wuhan, 430072, China.

出版信息

Anal Chim Acta. 2021 Nov 22;1186:339134. doi: 10.1016/j.aca.2021.339134. Epub 2021 Oct 2.

DOI:10.1016/j.aca.2021.339134
PMID:34756259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8486417/
Abstract

In recent years, single particle inductively coupled plasma mass spectrometry (SP-ICP-MS) has become a powerful tool for biological quantitative analysis. Homogeneous analysis method requires no separation and washing steps, which is suited for the analysis of highly infectious pathogens, so as to reduce the risk of infection during the operation. SARS-CoV-2 spreads all over the world, and its early infection symptoms are similar to influenza, which brings inconvenience to triage. Therefore, developing novel analytical method for simultaneous detection of multiple viral nucleic acids is essential. Taking the advantages of SP-ICP-MS and homogeneous analysis strategy, a SP-ICP-MS homogeneous nucleic acid assay by using gold nanoparticles (Au NPs) and silver nanoparticles (Ag NPs) probes was established for simultaneous sensitive analysis of SARS-CoV-2 and influenza A (H3N2). In the present of target SARS-CoV-2 or H3N2 nucleic acids, corresponding Au NPs or Ag NPs probes form larger aggregates, resulting in increased pulse signal intensity and reduced pulse signal frequency of the corresponding NPs in SP-ICP-MS measurement. In this assay, the reaction system of Au NPs and Ag NPs probes does not interfere with each other, and there was no separation and washing procedure, which facilitates operation, saves the analysis time, and improves the analysis efficiency. The linear range of this method is 5-1000 pmol L, with low-level limits of quantification of target nucleic acid. The developed SP-ICP-MS simultaneous homogeneous detection method has a good potential for detecting nucleic acid, protein, cell and other biological samples by changing different modification sequences on the NPs probes.

摘要

近年来,单颗粒电感耦合等离子体质谱(SP-ICP-MS)已成为生物定量分析的有力工具。均相分析方法无需分离和洗涤步骤,适用于高度传染性病原体的分析,从而降低操作过程中的感染风险。SARS-CoV-2 遍布全球,其早期感染症状与流感相似,给分诊带来不便。因此,开发用于同时检测多种病毒核酸的新型分析方法至关重要。本研究利用 SP-ICP-MS 和均相分析策略的优势,建立了一种基于金纳米粒子(Au NPs)和银纳米粒子(Ag NPs)探针的 SP-ICP-MS 均相核酸测定法,用于同时灵敏分析 SARS-CoV-2 和甲型流感(H3N2)。在存在靶标 SARS-CoV-2 或 H3N2 核酸的情况下,相应的 Au NPs 或 Ag NPs 探针形成更大的聚集体,导致 SP-ICP-MS 测量中相应 NPs 的脉冲信号强度增加和脉冲信号频率降低。在该测定法中,Au NPs 和 Ag NPs 探针的反应体系互不干扰,无需分离和洗涤步骤,操作简便,节省分析时间,提高了分析效率。该方法的线性范围为 5-1000 pmol L,具有低水平的定量下限。通过改变 NPs 探针上的不同修饰序列,开发的 SP-ICP-MS 同时均相检测方法具有检测核酸、蛋白质、细胞和其他生物样品的良好潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/a28886ab6e4a/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/0fb7a3eb1b86/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/f389e908e880/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/a14d239c352c/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/0d24f49b70ef/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/e40118b18a5a/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/4ec32698ec8b/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/bf2918f0e427/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/a28886ab6e4a/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/0fb7a3eb1b86/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/f389e908e880/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/a14d239c352c/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/0d24f49b70ef/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/e40118b18a5a/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/4ec32698ec8b/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/bf2918f0e427/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9117/8486417/a28886ab6e4a/gr7_lrg.jpg

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