Multicomponent nucleic acid enzymes as signal amplification strategy for the detection of microRNA based on fluorescence resonance energy transfer

IF 5.3 2区 化学 Q1 CHEMISTRY, ANALYTICAL Microchimica Acta Pub Date : 2025-02-25 DOI:10.1007/s00604-025-07002-6
Adrián Sánchez-Visedo, Patricia Alcázar-González, Luis José Royo, Ana Soldado, Francisco Javier Ferrero, José Manuel Costa-Fernández, María Teresa Fernández-Argüelles
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Abstract

A novel and simple methodology is introduced that allows accurate and highly sensitive detection of microRNAs (miRNAs), taking advantage of an amplification strategy based on multicomponent nucleic acid enzymes (MNAzymes), combined with a fluorescence resonance energy transfer (FRET) phenomenon. For this purpose, a fluorescent dye (FAM) has been selected as an energy donor, while gold nanoparticles (AuNPs) are employed as energy acceptors, located close to each other through hybridisation with the substrate. The research object was miR146a, which is a biomarker whose overexpression in milk is associated with inflammation in bovine mammary glands caused by bovine mastitis. The presence of a genetic target activates the MNAzyme cleavage capability, splitting the substrate into two parts. Hence, the presence of the target increases the distance between donor and acceptor, recovering the quenched fluorescence. Experimental parameters have been optimised, achieving a limit of detection (LOD) of only 2.3 fM (highly competitive as compared to other similar approaches) and a wide linear response range between 15.9 fM and 10 nM. In addition, the proposed methodology allows discriminating miR146a from other similar miRNAs differing in a single base mismatch. Detection of miR146a has been successfully carried out in spiked raw milk samples.

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基于荧光共振能量转移的多组分核酸酶作为信号扩增策略检测microRNA
介绍了一种新颖而简单的方法,利用基于多组分核酸酶(MNAzymes)的扩增策略,结合荧光共振能量转移(FRET)现象,可以准确和高灵敏度地检测microRNAs (miRNAs)。为此,选择荧光染料(FAM)作为能量供体,而金纳米颗粒(AuNPs)作为能量受体,通过与底物杂交而彼此靠近。研究对象为miR146a,这是一种生物标志物,其在牛奶中的过表达与牛乳腺炎引起的牛乳腺炎症有关。基因靶标的存在激活了MNAzyme的切割能力,将底物分成两部分。因此,靶的存在增加了供体和受体之间的距离,恢复了猝灭的荧光。实验参数经过优化,检测限(LOD)仅为2.3 fM(与其他类似方法相比极具竞争力),线性响应范围在15.9 fM至10 nM之间。此外,所提出的方法允许将miR146a与其他类似的mirna区分开来,这些mirna在单个碱基错配上存在差异。miR146a的检测已成功地在加标原料奶样品中进行。图形抽象
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来源期刊
Microchimica Acta
Microchimica Acta 化学-分析化学
CiteScore
9.80
自引率
5.30%
发文量
410
审稿时长
2.7 months
期刊介绍: As a peer-reviewed journal for analytical sciences and technologies on the micro- and nanoscale, Microchimica Acta has established itself as a premier forum for truly novel approaches in chemical and biochemical analysis. Coverage includes methods and devices that provide expedient solutions to the most contemporary demands in this area. Examples are point-of-care technologies, wearable (bio)sensors, in-vivo-monitoring, micro/nanomotors and materials based on synthetic biology as well as biomedical imaging and targeting.
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