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Amplified electrochemical genotyping of single-nucleotide polymorphisms using a graphene-gold nanoparticles modified glassy carbon platform

机译:使用石墨烯-金纳米颗粒修饰的玻碳平台对单核苷酸多态性进行电化学基因分型

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The main challenges in the construction of DNA biosensors for the genotyping of all the possible singlenucleotide polymorphisms (SNPs) are their sensitivity, speed and cost. The application of nanoparticle-modified monobases for the electrochemical genotyping of SNPs has been investigated in our previous study. In the present manuscript, that strategy was modified by applying a graphene-gold nanoparticle (GR-AuNPs) nanocomposite to achieve further amplification and higher sensitivity of SNPs genotyping. The present strategy shows a good potential for sensitively discriminating, quantifying and genotyping different SNPs. Taking the advantages of triple-amplification effects of AuNPs, GR and modified metal (Au and Ag) nanoparticles, this DNA biosensor exhibits highly sensitive responses for the genotyping of different SNPs and the detection of thermodynamically stable SNP (G-T) and A-C mismatch targets in the range of 10-1700 pM and 20-1200 pM with the detection limits of 2 and 10 pM (3 sigma) for G-T and A-C mismatch targets, respectively. The results demonstrate that when the surface coverage of DNA per unit area is just slightly increased, there is a dramatic increase in the active surface area, and the absolute loading amount of DNA on the surface would also be increased.
机译:用于所有可能的单核苷酸多态性(SNP)基因分型的DNA生物传感器的构建中的主要挑战是其灵敏度,速度和成本。在我们以前的研究中已经研究了纳米粒子修饰的单碱基在SNPs的电化学基因分型中的应用。在本手稿中,通过应用石墨烯-金纳米颗粒(GR-AuNPs)纳米复合材料对该策略进行了修改,以实现SNPs基因分型的进一步扩增和更高的敏感性。本策略显示出敏感区分,定量和基因分型不同SNPs的良好潜力。利用AuNPs,GR和修饰的金属(Au和Ag)纳米颗粒的三重放大作用,这种DNA生物传感器对不同SNP的基因分型以及热力学稳定的SNP(GT)和AC不匹配靶标的检测显示出高度敏感的响应。 GT和AC不匹配目标的检测限分别为10-1700 pM和20-1200 pM,检测限分别为2和10 pM(3 sigma)。结果表明,当每单位面积的DNA的表面覆盖率仅略微增加时,有效表面积会急剧增加,并且表面上DNA的绝对负载量也会增加。

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