Department of Chemistry , Iowa State University , Ames , Iowa 50011 United States.
Anal Chem. 2019 Jun 4;91(11):6991-6995. doi: 10.1021/acs.analchem.9b01762. Epub 2019 May 23.
Loop-mediated isothermal amplification (LAMP) is a powerful nucleic acid amplification technique due to its rapid and sensitive nature. These characteristics, in addition to low-cost and robustness, make LAMP an attractive alternative to polymerase chain reaction for point-of-care applications. However, sequence-specific detection remains a formidable challenge, particularly when single-nucleotide resolution is required. In this study, a LAMP method is developed for facile visual detection of single-nucleotide polymorphisms (SNPs) using molecular beacons (MBs) by exploiting the dual-fluorescence of fluorescein (6-FAM) and hydoxynaphthol blue (HNB). The method is coupled with solid-phase microextraction (SPME) to facilitate rapid extraction and detection of the target sequence. This work expands the use of MBs in LAMP for the visual detection of SNPs and facilitates the development of future LAMP assays for a wide-range of targets.
环介导等温扩增(LAMP)是一种强大的核酸扩增技术,因为其具有快速和敏感的特性。这些特性,加上低成本和稳健性,使得 LAMP 成为聚合酶链反应(PCR)在即时检测应用中的有吸引力的替代方法。然而,序列特异性检测仍然是一个艰巨的挑战,特别是当需要单核苷酸分辨率时。在这项研究中,开发了一种使用分子信标(MBs)通过利用荧光素(6-FAM)和羟萘酚蓝(HNB)的双重荧光来轻松进行单核苷酸多态性(SNP)的 LAMP 方法进行可视化检测。该方法与固相微萃取(SPME)相结合,以促进目标序列的快速提取和检测。这项工作扩展了 MBs 在 LAMP 中用于 SNP 的可视化检测的用途,并为未来用于广泛目标的 LAMP 检测方法的发展提供了便利。