High-throughput SNP genotyping based on solid-phase PCR on magnetic nanoparticles with dual-color hybridization

被引:58
作者
Liu, Hongna
Liab, Song
Wang, Zhifei
Ji, Meiju
Nie, Libo
He, Nongyue [1 ]
机构
[1] Southeast Univ, Sch Biol Sci & Med Engn, Chien Shiung Wu Lab, State Key Lab Bioelect, Nanjing 210096, Peoples R China
[2] Hunan Univ Technol, Key Lab Green Packaging & Applicat Biol Nanotechn, Zhuzhou 412008, Peoples R China
基金
中国国家自然科学基金;
关键词
magnetic nanoparticles; single nucleotide polymorphisms; solid-phase PCR; dual-color hybridization;
D O I
10.1016/j.jbiotec.2007.06.023
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Single-nucleotide polymorphisms (SNPs) are one-base variations in DNA sequence that can often be helpful when trying to find genes responsible for inherited diseases. In this paper, a microarray-based method for typing single nucleotide polymorphisms (SNPs) using solid-phase polymerase chain reaction (PCR) on magnetic nanoparticles (MNPs) was developed. One primer with biotin-label was captured by streptavidin coated magnetic nanoparticles (SA-MNPs), and PCR products were directly amplified on the surface of SA-MNPs in a 96-well plate. The samples were interrogated by hybridization with a pair of dual-color probes to determine SNP, and then genotype of each sample can be simultaneously identified by scanning the microarray printed with the denatured fluorescent probes. The C677T polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene from 126 samples were interrogated using this method. The results showed that three different genotypes were discriminated by three fluorescence patterns on the microarray. Without any purification and reduction procedure, and all reactions can be performed in the same vessel, this approach will be a simple and labor-saving method for SNP genotyping and can be applicable towards the automation system to achieve high-throughput SNP detection. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:217 / 222
页数:6
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