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首页> 外文期刊>Analytical and bioanalytical chemistry >A three-line lateral flow biosensor for logic detection of microRNA based on Y-shaped junction DNA and target recycling amplification
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A three-line lateral flow biosensor for logic detection of microRNA based on Y-shaped junction DNA and target recycling amplification

机译:三线横向流动生物传感器,用于基于Y型连接DNA和靶标循环扩增的microRNA逻辑检测

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摘要

A rapid, sensitive, and accurate detection strategy for microRNA 16 (miR-16) was developed, which combined the convenience of lateral flow biosensors (LFBs), the design flexibility of Y-shaped junction DNA probe, and the enhancement ability of endonuclease-assisted target recycling amplification. The system is composed of a molecular beacon (MB) probe, an assistant probe, and endonuclease Nt.BbvCI, which plays the role of signal translation and amplification. In the presence of the target microRNAs (miRNAs), three chains of nucleic acid could hybridize with each other to form a Y-shaped junction structure, which could be recognized by the endonuclease Nt.BbvCI. The MB probe was efficiently cleaved by endonuclease and produced two new DNA fragments, while the regenerated assistant probe and target were hybridized to another MB probe and entered into the next cycle of the amplification. In this way, the detection of the readily biodegradable miRNA was turned into the detection of two DNA fragments in the LFB. Meanwhile, the detection of two different DNAs would improve the accuracy and effectively avoid false results. The amplified products containing DNA fragments were then applied to the lateral flow nucleic acid biosensor (LFNAB) with two test zones, on which specific DNA probes were designed. The formed DNA-DNA/gold nanoparticle (GNP) conjugates were captured and accumulated to produce two red bands in two test zones. The logic judgment of the two test zones provided more accurate and convincing results. Under optimal conditions, the visual detection limit of miR-16 in aqueous solutions was 0.1 pM, which is 100-1000 times lower than that of visual or colorimetric methods in the literature. It could be used for on-field and point-of-care testing and meet the urgent demand of sensitive and selective miRNA detection in remote rural areas without costly equipment. The system displayed good universality, compatibility, high specificity, and stability of miRNA detection, which revealed significant potentiality in biomedical diagnosis.
机译:开发了一种快速,灵敏和准确的microRNA 16(miR-16)检测策略,该策略结合了侧向流生物传感器(LFB)的便利性,Y形连接DNA探针的设计灵活性以及核酸内切酶-辅助目标回收放大。该系统由分子信标(MB)探针,辅助探针和核酸内切酶Nt.BbvCI组成,它们起信号翻译和放大作用。在目标microRNA(miRNA)存在的情况下,三条核酸链可以相互杂交形成Y形连接结构,可以被核酸内切酶Nt.BbvCI识别。 MB探针被核酸内切酶有效切割并产生了两个新的DNA片段,而再生的辅助探针和靶标则与另一个MB探针杂交并进入了下一个扩增循环。这样,将易于生物降解的miRNA的检测转换为LFB中两个DNA片段的检测。同时,检测两个不同的DNA将提高准确性,并有效避免错误结果。然后将含有DNA片段的扩增产物应用于带有两个测试区的横向核酸生物传感器(LFNAB),在该测试区上设计了特定的DNA探针。捕获并积聚形成的DNA-DNA /金纳米颗粒(GNP)共轭物,在两个测试区中产生两个红色条带。两个测试区的逻辑判断提供了更准确和令人信服的结果。在最佳条件下,水溶液中miR-16的视觉检测极限为0.1 pM,比文献中的视觉或比色法低100-1000倍。它可用于现场和现场测试,无需昂贵的设备即可满足偏远农村地区灵敏和选择性miRNA检测的迫切需求。该系统显示出良好的通用性,兼容性,高特异性和miRNA检测的稳定性,这显示了在生物医学诊断中的巨大潜力。

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