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基于 PNA-DNA 杂合三链体形成和目标循环催化发夹组装扩增的用于 microRNA 检测的高灵敏和强稳健电化学生物传感器。

A highly sensitive and robust electrochemical biosensor for microRNA detection based on PNA-DNA hetero-three-way junction formation and target-recycling catalytic hairpin assembly amplification.

机构信息

School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, 315211, PR China.

College of Science and Technology, Ningbo University, Ningbo, 315300, PR China.

出版信息

Talanta. 2024 Jan 1;266(Pt 1):125020. doi: 10.1016/j.talanta.2023.125020. Epub 2023 Aug 1.

Abstract

Robust and sensitive methods for the detection of microRNAs (miRNAs) are crucial in the clinical diagnosis of cancers. In this study, a novel electrochemical biosensor with high sensitivity for miRNA-21 detection is developed, which relies on the formation of a peptide nucleic acid (PNA)-DNA hetero-three-way junction (H3WJ) and target-recycling catalytic hairpin assembly (CHA) amplification. The electroneutral PNA probes are initially immobilized onto a gold electrode to construct the sensor. Upon introduction of miRNA-21, target-recycling CHA is initiated, resulting in abundant double-stranded CHA products. Subsequently, association between the PNA probes and these products leads to the formation of PNA-DNA H3WJs. Consequently, the electrode surface is densely populated with numerous electroactive Ferrocene (Fc) groups, resulting in a significantly amplified current response for highly sensitive detection of miRNA-21 at concentrations as low as 0.15 fM. This approach demonstrates remarkable specificity towards target miRNAs and can be utilized for quantitative monitoring of miRNA-21 expression in human cancer cells. More importantly, the sensor exhibits exceptional stability and shows a significant reduction in background noise during miRNA detection, making this method a highly promising sensing platform for monitoring various miRNA biomarkers to facilitate the diagnosis of diverse cancers.

摘要

用于检测 microRNAs(miRNAs)的稳健且灵敏的方法在癌症的临床诊断中至关重要。在这项研究中,开发了一种用于 miRNA-21 检测的新型高灵敏度电化学生物传感器,该传感器依赖于肽核酸(PNA)-DNA 异三链结(H3WJ)和靶标循环催化发夹组装(CHA)扩增的形成。最初将中性电 PNA 探针固定在金电极上以构建传感器。引入 miRNA-21 后,启动靶标循环 CHA,导致大量双链 CHA 产物。随后,PNA 探针与这些产物结合导致 PNA-DNA H3WJ 的形成。因此,电极表面密集存在许多电活性的二茂铁(Fc)基团,从而实现了对 miRNA-21 的高灵敏度检测,其浓度低至 0.15 fM。该方法对靶标 miRNA 表现出显著的特异性,可用于定量监测人癌细胞中 miRNA-21 的表达。更重要的是,该传感器在 miRNA 检测过程中表现出出色的稳定性,并显著降低了背景噪声,使其成为监测各种 miRNA 生物标志物以促进各种癌症诊断的极具前景的传感平台。

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