底漆(化妆品)
检出限
化学
生物传感器
小RNA
环介导等温扩增
组合化学
材料科学
纳米技术
计算生物学
DNA
色谱法
生物
生物化学
基因
有机化学
作者
Xinyu Li,Xinmin Li,Dandan Li,Min Zhao,Haiping Wu,Bo Shen,Ping Liu,Shijia Ding
标识
DOI:10.1016/j.bios.2020.112554
摘要
Exosomal miRNAs have been discovered as important and reliable biomarkers for early diagnosis of tumors. However, it is still challenging to achieve accurate determination of trace exosomal miRNAs in real samples. Herein, we report an electrochemical strategy based on the cascade primer exchange reaction (PER) with [email protected]@MOF nanozyme for ultrasensitive detection of exosomal miRNA. Target-triggered PER that only includes a gated hairpin, a primer, and DNA polymerase can produce a long single strand in an autonomous and isothermal manner. Then, the nascent strand releases the protector B used to blockade capture probes, resulting in the binding of the nanozyme to sensing interface. Under the catalysis of the nanozyme, hydrogen peroxide (H2O2) is decomposed into H2O and O2, thus producing an amplified electrochemical signal. Benefiting from the cascade PER and the noticeable catalytic activity of the multiple-layered nanozyme, the established biosensor shows high sensitivity with limit of detection down to 0.29 fM and high specificity that can distinguish homologous miRNAs with single base mismatch. The developed strategy allows discrimination of tumor cells and breast cancer patients by detecting exosomal miRNA-21, and the results of this biosensor are consistent with qRT-PCR. Therefore, the electrochemical strategy has wide potential in the early screening of tumors.
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