A Novel miRNA Detection Method Using Loop-Mediated Isothermal Amplification

被引:3
|
作者
Wu, Saiwei [1 ]
Al-Maskri, Abdu Ahmed Abdullah [2 ]
Li, Qun [1 ]
Liu, Jiatong [2 ]
Cai, Sheng [2 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 4, Sch Med, Dept Pharm, Yiwu, Zhejiang, Peoples R China
[2] Zhejiang Univ, Inst Drug Metab & Pharmaceut Anal, Coll Pharmaceut Sci, Hangzhou 310058, Zhejiang, Peoples R China
关键词
STRAND-DISPLACEMENT AMPLIFICATION; ROLLING CIRCLE AMPLIFICATION; ULTRASENSITIVE DETECTION; MICRORNAS; PLATFORM;
D O I
10.1155/2023/6624884
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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.
引用
收藏
页数:8
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