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基于镧系纳米颗粒标记策略的 SARS-CoV-2 多重核酸检测

Multiplex Nucleic Acid Assay of SARS-CoV-2 via a Lanthanide Nanoparticle-Tagging Strategy.

机构信息

Analytical & Testing Center, Sichuan University, Chengdu 610064, Sichuan, China.

Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, Sichuan, China.

出版信息

Anal Chem. 2021 Sep 21;93(37):12714-12722. doi: 10.1021/acs.analchem.1c02657. Epub 2021 Sep 8.

Abstract

Early diagnosis, early isolation, and early treatment are efficient solutions to control the COVID-19 pandemic. To achieve the accurate early diagnosis of SARS-CoV-2, a multiplex detection strategy is required for the cross-validation to solve the problem of "false negative" of the existing gold standard assay. Here, we present a multicomponent nucleic acid assay platform for SARS-CoV-2 detection based on lanthanide nanoparticle (LnNP)-tagging strategy. For targeting SARS-CoV-2's RNA fragments ORF1ab gene, RdRp gene, and E gene, three LnNP probes can be used simultaneously to identify three sites in one sample through elemental mass spectrometry detection with limits of detection of 1.2, 1.3, and 1.3 fmol, respectively. With the multisite cross-validation, we envision that this multiplex and sensitive detection platform may provide an effective strategy for SARS-CoV-2 fast screening with a high accuracy.

摘要

早期诊断、早期隔离和早期治疗是控制 COVID-19 大流行的有效方法。为了实现对 SARS-CoV-2 的准确早期诊断,需要采用多重检测策略进行交叉验证,以解决现有金标准检测方法“假阴性”的问题。在这里,我们提出了一种基于镧系纳米粒子(LnNP)标记策略的 SARS-CoV-2 检测多组分核酸检测平台。针对 SARS-CoV-2 的 RNA 片段 ORF1ab 基因、RdRp 基因和 E 基因,可同时使用三种 LnNP 探针,通过元素质谱检测鉴定一个样本中的三个位点,检测限分别为 1.2、1.3 和 1.3 fmol。通过多站点交叉验证,我们设想这种多重和敏感的检测平台可能为 SARS-CoV-2 的快速筛查提供一种具有高准确性的有效策略。

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