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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Visual detection of gene mutations based on isothermal strand-displacement polymerase reaction and lateral flow strip
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Visual detection of gene mutations based on isothermal strand-displacement polymerase reaction and lateral flow strip

机译:基于等温链置换聚合酶反应和侧流条的视觉检测基因突变

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摘要

Here, we describe a simple and sensitive approach for visual detection of gene mutations based on isothermal strand-displacement polymerase reactions (ISDPR) and lateral flow strip (LFS). The concept was first demonstrated by detecting the R156H-mutant gene of keratin 10 in Epidermolytic hyperkeratosis (EHK). In the presence of biotin-modified hairpin DNA and digoxin-modified primer, the R156H-mutant DNA triggered the ISDPR to produce numerous digoxin- and biotin-attached duplex DNA products. The product was detected on the LFS through dual immunoreactions (anti-digoxin antibody on the gold nanoparticle (Au-NP) and digoxin on the duplex, anti-biotin antibody on the LFS test zone and biotin on the duplex). The accumulation of Au-NPs produced the characteristic red band, enabling visual detection of the mutant gene without instrumentation. After systematic optimization of the ISDPR experimental conditions and the parameters of the assay, the current approach was capable of detecting as low as 1-fM R156H-mutant DNA within 75. min without instrumentation. Differentiation of R156H- and R156C-mutant DNA on the R156 mutation site was realized by using fluorescein- and biotin-modified hairpin probes in the ISDPR process. The approach thus provides a simple, sensitive, and low-cost tool for the detection of gene mutations.
机译:在这里,我们描述了一种基于等温链置换聚合酶反应(ISDPR)和侧向流动试纸(LFS)的视觉检测基因突变的简单而灵敏的方法。该概念首先通过在表皮过度角化病(EHK)中检测角蛋白10的R156H突变基因得到证实。在存在生物素修饰的发夹DNA和地高辛修饰的引物的情况下,R156H突变型DNA触发了ISDPR产生大量地高辛和生物素连接的双链DNA产物。通过双重免疫反应(金纳米颗粒上的抗地高辛抗体(Au-NP)和双链体上的地高辛,LFS测试区的抗生物素抗体和双链体上的生物素)在LFS上检测到了该产物。 Au-NPs的积累产生了特征性的红色条带,无需仪器即可目视检测突变基因。在对ISDPR实验条件和测定参数进行系统优化之后,当前方法无需仪器即可在75分钟内检测低至1-fM R156H突变DNA。通过在ISDPR过程中使用荧光素和生物素修饰的发夹探针实现R156突变位点上R156H和R156C突变DNA的区分。因此,该方法提供了一种简单,灵敏且低成本的工具来检测基因突变。

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