核酸酶
复式(建筑)
化学
小RNA
计算生物学
检出限
临床诊断
聚合酶链反应
DNA
分子生物学
基因
生物
色谱法
生物化学
医学
临床心理学
作者
Limei Zhang,Zhang Zhang,Jingling Xie,Yuanqing Zhao,Gang Tian,Hui Jiang,Hualin Tao,Jinbo Liu
标识
DOI:10.1016/j.aca.2021.339182
摘要
Dysregulation of MicroRNAs (miRNAs) cause various diseases in humans, and developing reliable methods to detect miRNAs is critical for molecular diagnostics and personalized medicine. This study developed a toehold-mediated target invasion combined with duplex-specificity nuclease (DSN)-assisted cyclic signal amplification fluorescent sensor. Herein, we take advantage of toehold-mediated target invasion process to ensure the high selectivity of miRNA determination, coupled with the unique cleavage properties of DSN to improve the sensitivity of the strategy significantly. Throughout the assay, the whole procedure of detection the target let-7a has a limit of detection (LOD) as low as 9.00 fM and an excellent linear range from 1 pM to 100 nM for no more than 60 min. The assay shows reasonable specificity in detecting mismatched miRNAs and can realize single-base discrimination in the let-7 families. Finally, the developed method was applied to detect the miRNAs extracted from human serum. The results were consistent with those based on the quantitative reverse transcription-polymerase chain reaction(qRT-PCR) method, which shows great potential application value in clinical molecular diagnostics and biological research.
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