A Novel SNPs Detection Method Based on Gold Magnetic Nanoparticles Array and Single Base Extension

被引:220
作者
Li, Song [1 ,2 ]
Liu, Hongna [2 ]
Jia, Yingying [2 ]
Deng, Yan [1 ,2 ]
Zhang, Liming [1 ,2 ]
Lu, Zhuoxuan [1 ,2 ]
He, Nongyue [1 ,2 ]
机构
[1] Hunan Univ Technol, Hunan Key Lab Green Packaging & Applicat Biol Nan, Zhuzhou 412007, Peoples R China
[2] Southeast Univ, State Key Lab Bioelect, Dept Biol Sci & Med Engn, Nanjing 210096, Jiangsu, Peoples R China
基金
中国博士后科学基金;
关键词
Magnetic beads; Dual-color SBE; Single nucleotide polymorphisms; Gold magnetic nanoparticles; Microarray; GENOME-WIDE DETECTION; POLYMORPHISMS; HYBRIDIZATION; FABRICATION; RESOLUTION; ACCURATE; DISEASE;
D O I
10.7150/thno.5032
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
To fulfill the increasing need for large-scale genetic research, a high-throughput and automated SNPs genotyping method based on gold magnetic nanoparticles (GMNPs) array and dual-color single base extension has been designed. After amplification of DNA templates, biotinylated extension primers were captured by streptavidin coated gold magnetic nanoparticle (SA-GMNPs). Next a solid-phase, dual-color single base extension (SBE) reaction with the specific biotinylated primer was performed directly on the surface of the GMNPs. Finally, a "bead array" was fabricated by spotting GMNPs with fluorophore on a clean glass slide, and the genotype of each sample was discriminated by scanning the "bead array". MTHFR gene C677T polymorphism of 320 individual samples were interrogated using this method, the signal/noise ratio for homozygous samples were over 12.33, while the signal/noise ratio for heterozygous samples was near 1. Compared with other dual-color hybridization based genotyping methods, the method described here gives a higher signal/noise ratio and SNP loci can be identified with a high level of confidence. This assay has the advantage of eliminating the need for background subtraction and direct analysis of the fluorescence values of the GMNPs to determine their genotypes without the necessary procedures for purification and complex reduction of PCR products. The application of this strategy to large-scale SNP studies simplifies the process, and reduces the labor required to produce highly sensitive results while improving the potential for automation.
引用
收藏
页码:967 / 975
页数:9
相关论文
共 36 条
[1]  
Barreiro LB, 2009, METHODS MOL BIOL, V578, P255, DOI 10.1007/978-1-60327-411-1_17
[2]  
Bell PA, 2002, BIOTECHNIQUES, P70
[3]   Integrin Targeted Imaging and Therapy [J].
Chen, Xiaoyuan .
THERANOSTICS, 2011, 1 :28-29
[4]   Variations on a theme: Cataloging human DNA sequence variation [J].
Collins, FS ;
Guyer, MS ;
Chakravarti, A .
SCIENCE, 1997, 278 (5343) :1580-1581
[5]   Highly parallel genomic assays [J].
Fan, Jian-Bing ;
Chee, Mark S. ;
Gunderson, Kevin L. .
NATURE REVIEWS GENETICS, 2006, 7 (08) :632-644
[6]   A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE [J].
FROSST, P ;
BLOM, HJ ;
MILOS, R ;
GOYETTE, P ;
SHEPPARD, CA ;
MATTHEWS, RG ;
BOERS, GJH ;
DENHEIJER, M ;
KLUIJTMANS, LAJ ;
VANDENHEUVEL, LP ;
ROZEN, R .
NATURE GENETICS, 1995, 10 (01) :111-113
[7]   Preparation of Anti-CD40 Antibody Modified Magnetic PCL-PEG-PCL Microspheres [J].
Gao, Xiang ;
Kan, Bing ;
Gou, MaLing ;
Zhang, Juan ;
Guo, Gang ;
Huang, Ning ;
Zhao, Xia ;
Qian, ZhiYong .
JOURNAL OF BIOMEDICAL NANOTECHNOLOGY, 2011, 7 (02) :285-291
[8]   Distinguishing different DNA heterozygotes by high-resolution melting [J].
Graham, R ;
Liew, M ;
Meadows, C ;
Lyon, E ;
Wittwer, CT .
CLINICAL CHEMISTRY, 2005, 51 (07) :1295-1298
[9]   Genome-wide detection of polymorphisms at nucleotide resolution with a single DNA microarray [J].
Gresham, D ;
Ruderfer, DM ;
Pratt, SC ;
Schacherer, J ;
Dunham, MJ ;
Botstein, D ;
Kruglyak, L .
SCIENCE, 2006, 311 (5769) :1932-1936
[10]   A genome-wide scalable SNP genotyping assay using microarray technology [J].
Gunderson, KL ;
Steemers, FJ ;
Lee, G ;
Mendoza, LG ;
Chee, MS .
NATURE GENETICS, 2005, 37 (05) :549-554