Wu Saiwei, Abdullah Al-Maskri Abdu Ahmed, Li Qun, Liu Jiatong, Cai Sheng
Department of Pharmacy, The Fourth Affiliated Hospital, Zhejiang University School of Medicine, Yiwu, Zhejiang, China.
Institute of Drug Metabolism and Pharmaceutical Analysis, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China.
Int J Anal Chem. 2023 Sep 12;2023:6624884. doi: 10.1155/2023/6624884. eCollection 2023.
A novel ligation-based loop-mediated isothermal amplification has been developed for miRNA detection. Two stem-loop structure DNA linker A/B probes which hybridized with miRNA were designed to establish a rapid and ultrasensitive miRNA-LAMP system for miRNA detection. Target miR-200a was used to template the ligation of Linker A/B probes with SplintR Ligase and used as a dumbbell-shaped amplicon. By adding BIP/FIP and Bst 2.0 DNA polymerase, the LAMP reaction was carried out, which brought greatly improved amplification efficiency. The double-stranded DNA fluorescent dye EvaGreen was added for the detection of amplification product to achieve the quantification of the target miRNA. This method can detect miRNA in a linear range of seven orders of magnitude, with a detection limit of 100 fM. Therefore, this ultrasensitive miRNA-LAMP assay provides a new path for the highly sensitive quantitative analysis of miRNA, thereby bringing convenience to clinical diagnosis and prognostic research.
一种基于连接的新型环介导等温扩增技术已被开发用于miRNA检测。设计了两种与miRNA杂交的茎环结构DNA连接子A/B探针,以建立一种用于miRNA检测的快速、超灵敏的miRNA-LAMP系统。以靶标miR-200a为模板,用SplintR连接酶连接连接子A/B探针,并用作哑铃形扩增子。通过添加BIP/FIP和Bst 2.0 DNA聚合酶进行LAMP反应,大大提高了扩增效率。加入双链DNA荧光染料EvaGreen用于检测扩增产物,以实现对靶标miRNA的定量。该方法可在七个数量级的线性范围内检测miRNA,检测限为100 fM。因此,这种超灵敏的miRNA-LAMP检测方法为miRNA的高灵敏定量分析提供了一条新途径,从而为临床诊断和预后研究带来便利。