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基于磁性纳米颗粒的聚合酶链式反应扩增:在高通量单核苷酸多态性基因分型中的应用

PCR amplification on magnetic nanoparticles: application for high-throughput single nucleotide polymorphism genotyping.

作者信息

Liu Hongna, Li Song, Wang Zhifei, Hou Peng, He Quanguo, He Nongyue

机构信息

Key Laboratory of Green Packaging and Application of Biological Nanotechnology of Hunan Province, Hunan University of Technology, Zhuzhou, China.

出版信息

Biotechnol J. 2007 Apr;2(4):508-11. doi: 10.1002/biot.200600214.

Abstract

A novel approach for the genotyping of single nucleotide polymorphisms (SNPs) based on solidphase PCR on magnetic nanoparticles (MNPs) is described. PCR products were amplified directly on MNPs. The genotypes of a given SNP were differentiated by hybridization with a pair of allele-specific probes labeled with dual-color fluorescence (Cy3, Cy5). The results were analyzed by scanning the microarray printed with the denatured fluorescent probes on an unmodified glass slide. Electrophoresis analysis indicated that PCR could proceed successfully when MNPs-bound primers were used. Furthermore, nine different samples were genotyped and their fluorescent signals were quantified. Genotyping results showed that three genotypes for the locus were very easily discriminated. The fluorescent ratios (match probe:mismatch probe signal) of homozygous samples were over 9.3, whereas heterozygous samples had ratios near 1.0. Without any purification and concentration of PCR products, this new MNP-PCR based genotyping assay potentially provides a rapid, labor-saving method for genotyping of a large number of individuals.

摘要

描述了一种基于磁性纳米颗粒(MNPs)上的固相PCR对单核苷酸多态性(SNPs)进行基因分型的新方法。PCR产物直接在MNPs上扩增。通过与一对用双色荧光(Cy3、Cy5)标记的等位基因特异性探针杂交来区分给定SNP的基因型。通过扫描在未修饰的载玻片上印刷有变性荧光探针的微阵列来分析结果。电泳分析表明,当使用与MNPs结合的引物时,PCR可以成功进行。此外,对九个不同的样品进行了基因分型并对其荧光信号进行了定量。基因分型结果表明,该位点的三种基因型很容易区分。纯合样品的荧光比率(匹配探针:错配探针信号)超过9.3,而异合子样品的比率接近1.0。无需对PCR产物进行任何纯化和浓缩,这种基于MNP-PCR的新基因分型测定法可能为大量个体的基因分型提供一种快速、省力的方法。

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