Automated detection system of single nucleotide polymorphisms using two kinds of functional magnetic nanoparticles

被引:32
作者
Liu, Hongna [1 ]
Li, Song [1 ,2 ]
Wang, Zhifei [3 ]
Li, Zhiyang [1 ]
Deng, Yan [1 ,2 ]
Wang, Hua [4 ]
Shi, Zhiyang [4 ]
He, Nongyue [1 ,2 ]
机构
[1] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Nanjing 210096, Peoples R China
[2] Hunan Univ Technol, Hunan Key Lab Green Packaging & Applicat Biol Nan, Zhuzhou 412008, Peoples R China
[3] Southeast Univ, Sch Chem & Chem Engn, Nanjing 210096, Peoples R China
[4] Ctr Dis Prevent & Control Jiangsu Prov, Minist Hlth, Key Lab Enter Pathogen Microbiol, Nanjing 210009, Peoples R China
关键词
Magnetic nanoparticles; SNPs; Automated workstation; Dual-color hybridization;
D O I
10.1016/j.apsusc.2008.06.117
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Single nucleotide polymorphisms (SNPs) comprise the most abundant source of genetic variation in the human genome wide codominant SNPs identification. Therefore, large-scale codominant SNPs identification, especially for those associated with complex diseases, has induced the need for completely high-throughput and automated SNP genotyping method. Herein, we present an automated detection system of SNPs based on two kinds of functional magnetic nanoparticles (MNPs) and dual-color hybridization. The amido-modified MNPs (NH(2)-MNPs) modified with APTES were used for DNA extraction from whole blood directly by electrostatic reaction, and followed by PCR, was successfully performed. Furthermore, biotinylated PCR products were captured on the streptavidin-coated MNPs (SA-MNPs) and interrogated by hybridization with a pair of dual-color probes to determine SNP, then the genotype of each sample can be simultaneously identified by scanning the microarray printed with the denatured fluorescent probes. This system provided a rapid, sensitive and highly versatile automated procedure that will greatly facilitate the analysis of different known SNPs in human genome. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:600 / 603
页数:4
相关论文
共 10 条
[1]   Highly parallel genomic assays [J].
Fan, Jian-Bing ;
Chee, Mark S. ;
Gunderson, Kevin L. .
NATURE REVIEWS GENETICS, 2006, 7 (08) :632-644
[2]   In situ DNA amplification with magnetic primers for the electrochemical detection of food pathogens [J].
Lermo, A. ;
Campoy, S. ;
Barbe, J. ;
Hernandez, S. ;
Alegret, S. ;
Pividori, M. I. .
BIOSENSORS & BIOELECTRONICS, 2007, 22 (9-10) :2010-2017
[3]   Application of microarray-based method for methylenetetrahydrofolate reductase (MTHFR) polymorphisms in the risk of gastric carcinoma in East China population [J].
Li, Song ;
Ji, Meiju ;
He, Nongyue ;
Lu, Zuhong .
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2007, 7 (09) :3245-3249
[4]   High-throughput SNP detection using nano-scale engineered biomagnetite [J].
Matsunaga, Tadashi ;
Maruyama, Kohei ;
Takeyama, Haruko ;
Katoh, Takahiko .
BIOSENSORS & BIOELECTRONICS, 2007, 22 (9-10) :2315-2321
[5]  
Niemeyer CM, 2001, ANGEW CHEM INT EDIT, V40, P4128, DOI 10.1002/1521-3773(20011119)40:22<4128::AID-ANIE4128>3.0.CO
[6]  
2-S
[7]   Genome research - A closer look at SNPs suggests difficulties [J].
Pennisi, E .
SCIENCE, 1998, 281 (5384) :1787-1789
[8]   Synthesis and characterization of 3-aminopropyltriethoxysilane-modified superparamagnetic magnetite nanoparticles [J].
Shen, XC ;
Fang, XZ ;
Zhou, YH ;
Liang, H .
CHEMISTRY LETTERS, 2004, 33 (11) :1468-1469
[9]   Population distribution of high. sensitivity C-reactive protein values in Aboriginal Australians: A comparison with other populations [J].
Wang, ZQ ;
Hoy, WE .
CLINICAL BIOCHEMISTRY, 2006, 39 (03) :277-281
[10]   Single nucleotide polymorphism genotyping of aldehyde dehydrogenase 2 gene using a single bacterial magnetic particle [J].
Yoshino, T ;
Tanaka, T ;
Takeyama, H ;
Matsunaga, T .
BIOSENSORS & BIOELECTRONICS, 2003, 18 (5-6) :661-666