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利用分子信标实现基于侧流免疫层析的环介导等温扩增对 ORF1a、BRAF 和 ompW 基因序列的特异性检测

Sequence-Specific Detection of ORF1a, BRAF, and ompW DNA Sequences with Loop Mediated Isothermal Amplification on Lateral Flow Immunoassay Strips Enabled by Molecular Beacons.

机构信息

Department of Chemistry, Iowa State University, 1605 Gilman Hall, Ames, Iowa 50011, United States.

出版信息

Anal Chem. 2021 Mar 9;93(9):4149-4153. doi: 10.1021/acs.analchem.0c05355. Epub 2021 Feb 26.

DOI:10.1021/acs.analchem.0c05355
PMID:33635624
Abstract

Loop-mediated isothermal amplification (LAMP) holds great potential for point-of-care (POC) diagnostics due to its speed and sensitivity. However, differentiation between spurious amplification and amplification of the target sequence is a challenge. Herein, we develop the use of molecular beacon (MB) probes for the sequence-specific detection of LAMP on commercially available lateral flow immunoassay (LFIA) strips. The detection of three unique DNA sequences, including ORF1a from SARS-CoV-2, is demonstrated. In addition, the method is capable of detecting clinically relevant single-nucleotide polymorphisms (BRAF V600E). For all sequences tested, the LFIA method offers similar sensitivity to fluorescence detection using a qPCR instrument. We also demonstrate the coupling of the method with solid-phase microextraction to enable isolation and detection of the target sequences from human plasma, pond water, and artificial saliva. Lastly, a 3D printed device is designed and implemented to prevent contamination caused by opening the reaction containers after LAMP.

摘要

环介导等温扩增(LAMP)因其速度和灵敏度而在即时检测(POC)诊断方面具有巨大潜力。然而,区分假阳性扩增和目标序列扩增是一个挑战。在此,我们开发了使用分子信标(MB)探针进行 LAMP 的序列特异性检测,该方法可用于市售的侧向流动免疫分析(LFIA)条上。该方法可用于检测三种独特的 DNA 序列,包括 SARS-CoV-2 的 ORF1a。此外,该方法能够检测到临床相关的单核苷酸多态性(BRAF V600E)。对于所有测试的序列,LFIA 方法与使用 qPCR 仪器进行荧光检测的灵敏度相当。我们还展示了该方法与固相微萃取的结合,可从人血浆、池塘水和人工唾液中分离和检测目标序列。最后,设计并实现了一种 3D 打印设备,以防止在 LAMP 后打开反应容器引起的污染。

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