环介导等温扩增
多重位移放大
小RNA
级联
检出限
核酸
线性范围
熵(时间箭头)
纳米技术
生物系统
化学
计算生物学
组合化学
DNA
材料科学
生物
色谱法
聚合酶链反应
物理
生物化学
基因
DNA提取
量子力学
作者
Shu Ou,Tao Xu,Xi Liu,Xinyuan Yu,Rong Li,Jing Deng,Jinxian Yuan,Yangmei Chen
标识
DOI:10.1016/j.snb.2017.09.130
摘要
MicroRNAs (miRNAs) are potential biomarkers for early diagnosis of various diseases. Herein, we reported, for the first time, a simple and rapid fluorescence strategy for highly sensitive and specific detection of miRNA based on strand displacement amplification-mediated entropy-driven circuit reaction (SDA-EDCR). The binding of target miRNA with a hairpin template initiated SDA to cyclically generate large amounts of triggers. Then, the triggers could initiate EDCR to release report strands and cyclic reuse triggers, resulting in a significantly amplified fluorescence signal toward miRNA detection. The isothermal amplification method exhibited a much wider linear range from 1 fM to 10 nM with low detection limit of 0.18 fM. The strategy could also be applied to detect the miRNA in complex sample matrix with satisfied results. Moreover, the two-layer amplification strategy was time-saving in comparison with most of previously reported cascade amplification methods Therefore, this novel approach provides a general platform to develop simple, rapid, cost-effective, sensitive, and selective nucleic acids assay for various important applications in bioanalysis and clinical diagnosis.
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