基于双链特异性核酸酶和银纳米簇的无标记miRNA荧光生物传感器

IF 3.6 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Analyst Pub Date : 2024-12-18 DOI:10.1039/D4AN01407C
Yuxin Zheng, Qian Wang, Zhiying Jin, Tingting Zhang, Jianshe Huang, Jianshan Ye and Xiurong Yang
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引用次数: 0

摘要

MicroRNAs (miRNAs)被认为是多种疾病的可靠生物标志物。然而,其在生物体内的低丰度和同源mirna的高序列相似性使得其准确检测具有挑战性。本文基于双特异性核酸酶(DSN)辅助扩增和dna模板银纳米团簇(dna - agnc)作为荧光信号探针,构建了一种新型荧光生物传感器,用于检测miRNA-155,这是一种潜在的神经炎症生物标志物。dsn辅助扩增可以将不稳定的miRNA转化为稳定的DNA,同时放大miRNA信号。使用dna - agnc作为生物传感器的荧光信号探针可以避免复杂的标记过程,降低成本。该传感器具有良好的选择性和重复性,线性范围宽(1 ~ 600 nM),检出限为0.86 nM,具有实际样品检测的潜力。这项工作为miRNA检测提供了一个潜在的通用生物传感平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Label-free miRNA fluorescent biosensors based on duplex-specific nucleases and silver nanoclusters†

Label-free miRNA fluorescent biosensors based on duplex-specific nucleases and silver nanoclusters†

MicroRNAs (miRNAs) are considered reliable biomarkers for a variety of diseases. However, their low abundance in organisms and high sequence similarity of homologous miRNAs make their accurate detection challenging. Here, we constructed a novel fluorescent biosensor for the detection of miRNA-155, a potential biomarker of neuroinflammation, based on duplex-specific nuclease (DSN) assisted amplification and DNA-templated silver nanoclusters (DNA-AgNCs) as fluorescence signal probes. DSN-assisted amplification can transform unstable miRNA into stable DNA and amplify the miRNA signal at the same time. Using DNA-AgNCs as fluorescence signal probes for biosensors can avoid complex labeling processes and reduce costs. The biosensor shows excellent selectivity, reproducibility, a wide linear range (1–600 nM) with a detection limit of 0.86 nM, and potentiality for real sample detection. This work provides a potential universal biosensing platform for miRNA detection.

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来源期刊
Analyst
Analyst 化学-分析化学
CiteScore
7.80
自引率
4.80%
发文量
636
审稿时长
1.9 months
期刊介绍: "Analyst" journal is the home of premier fundamental discoveries, inventions and applications in the analytical and bioanalytical sciences.
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