化学
核酸外切酶
小RNA
检出限
生物传感器
核酸外切酶 III
多重位移放大
环介导等温扩增
动态范围
DNA
熵(时间箭头)
纳米技术
计算生物学
生物系统
组合化学
基因
聚合酶链反应
色谱法
计算机科学
生物化学
物理
生物
DNA提取
量子力学
DNA聚合酶
材料科学
大肠杆菌
计算机视觉
作者
Lanxin Nie,Xiaogang Zeng,Hongbo Li,Suqin Wang,Zhanghui Lu,Ru‐Qin Yu
标识
DOI:10.1016/j.aca.2023.341392
摘要
MicroRNAs (miRNAs) research in cancer diagnosis is expanding, on account of miRNAs were demonstrated to be key indicator of gene expression and hopeful candidates for biomarkers. In this study, a stable miRNA-let-7a fluorescent biosensor was successfully designed based on an exonuclease Ⅲ-assisted two-stage strand displacement reaction (SDR). First, an entropy-driven SDR containing a three-chain structure of the substrate is used in our designed biosensor, leading to reduce the reversibility of the target recycling process in each step. The target acts on the first stage to start the entropy-driven SDR, which generates the trigger used to stimulate the exonuclease Ⅲ-assisted SDR in the second stage. At the same time, we design a SDR one-step amplification strategy as a comparison. Expectly, this developed two-stage strand displacement system has a low detection limit of 25.0 pM as well as a broad detection range of 4 orders of magnitude, making it more sensitive than the SDR one-step sensor, whose detection limit is 0.8 nM. In addition, this sensor has high specificity across members of the miRNA family. Therefore, we can take advantage of this biosensor to promote miRNA research in cancer diagnosis sensing systems.
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