化学
连锁反应
哑铃
生物传感器
检出限
DNA
多重位移放大
小RNA
杂交探针
环介导等温扩增
DNA–DNA杂交
纳米技术
分子生物学
聚合酶链反应
基因
色谱法
生物化学
材料科学
DNA提取
医学
光化学
生物
物理疗法
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2020-07-27
卷期号:92 (17): 12026-12032
被引量:125
标识
DOI:10.1021/acs.analchem.0c02654
摘要
Exosomal miRNA is an ideal source of noninvasive biomarker for the diagnosis of cancer. Sensitive and accurate analysis of exosomal miRNA plays an important role in facilitating clinical applications. Herein, we have developed a novel electrochemical method for exosomal miRNA assay coupling strand displacement amplification (SDA) and dumbbell hybridization chain reaction (DHCR). The target triggered isothermal SDA process generates a large number of single-stranded DNA products to assist the formation of the three-way junction structure on the electrode surface. In addition, dumbbell DNA fuel strands (DHP1 and DHP2) are designed for the hybridization chain reaction. This novel form of HCR produces DNA nanostructures with a tight conformation, which facilitates the enhancement of the electrochemical response. The combination of the dual signal amplification significantly improves the sensitivity for the exosomal miRNA assay, resulting in a limit of detection (LOD) as low as 7.3 aM. More importantly, the method is successfully applied in the analysis of cells and human serum samples, which demonstrates the potential utility in point-of-care testing (POCT) applications.
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