基于氧化石墨烯的通过核酸外显酶III辅助双信号循环检测股骨头敏感骨坏死(ONFH)相关微小RNA的测定。

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Molecular Biotechnology Pub Date : 2024-11-01 Epub Date: 2023-10-18 DOI:10.1007/s12033-023-00924-7
Jian Yu, Kun Han
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引用次数: 0

摘要

循环微小RNA(miRNA)的准确检测在各种疾病的诊断中起着至关重要的作用。然而,目前的miRNA检测方法因其低灵敏度和过多的背景信号而受到广泛批评。在此,我们提出了一种基于氧化石墨烯(GO)的荧光生物传感器,通过利用核酸外切酶III(Exo III)辅助的靶循环和杂交链式反应(HCR),在低背景信号下进行灵敏可靠的miRNA分析。为了启动Exo III辅助的双信号循环,开发了一种用于选择性结合miRNA的发夹DNA探针(H探针)。当羧基荧光素(FAM)标记的发夹(HP1和HP1)不能与其预期靶标结合,而是通过p-粘附相互作用吸附在GO表面时,染料猝灭发生。Exo III在附着靶miRNA时顺序切割H探针和S探针的3'-链,导致miRNA的释放和“g”序列的自主产生。释放的靶miRNA随后与第二个H探针杂交并进入随后的反应阶段。在HP1和HP2探针的帮助下,当“g”序列触发HCR时,产生了长的dsDNA产物。dsDNA产物没有被GO吸收,而是发出明亮的荧光。结果,测量了感兴趣的miRNA的量。该生物测定的LOD仅为5.6fM,表现出优异的选择性和高灵敏度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Graphene Oxide-based Assay for Sensitive Osteonecrosis of the Femoral Head (ONFH) related microRNA Detection via Exonuclease-III Assisted Dual Signal Cycle.

Accurate detection of circulating microRNAs (miRNAs) plays a vital role in the diagnosis of various diseases. The current miRNA detection methods, however, are widely criticized for their low sensitivity and excessive background signal. Herein, we propose a graphene oxide (GO) based fluorescent biosensor for sensitive and reliable miRNA analysis with a low background signal by utilizing exonuclease III (Exo III)-assisted target recycling and hybridization chain reaction (HCR). To initiate Exo-III-assisted dual signal cycles, a hairpin DNA probe (H probe) was developed for selective miRNA binding. Dye quenching occurred when carboxyfluorescein (FAM)-labeled hairpins (HP1 and HP1) were unable to bind to their intended target and instead adsorb onto the surface of GO via p-stacking interactions. Exo III sequentially cleaved the 3'-strand of the H probe and the S probe upon attachment of the target miRNA, resulting in the release of the miRNA and the autonomous production of a "g" sequence. The released target miRNA then hybridized with a second H probe and progressed to the subsequent reaction phase. With the help of the HP1 and HP2 probes, a lengthy dsDNA product was produced when the "g" sequence triggered HCR. The dsDNA product was not absorbed by GO, and the material instead fluoresced brightly. As a result, the amount of miRNA of interest was measured. With a LOD of only 5.6 fM, this bioassay demonstrated excellent selectivity and great sensitivity.

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来源期刊
Molecular Biotechnology
Molecular Biotechnology 医学-生化与分子生物学
CiteScore
4.10
自引率
3.80%
发文量
165
审稿时长
6 months
期刊介绍: Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.
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