Department of Chemistry, Iowa State University, 1605 Gilman Hall, Ames, Iowa 50011, United States.
Anal Chem. 2021 Mar 9;93(9):4149-4153. doi: 10.1021/acs.analchem.0c05355. Epub 2021 Feb 26.
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.
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。