Automated detection system of single nucleotide polymorphisms using two kinds of functional magnetic nanoparticles |
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Authors: | Hongna Liu Song Li Zhifei Wang Yan Deng Hua Wang Nongyue He |
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Affiliation: | a State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, China b Hunan Key Laboratory of Green Packaging and Application of Biological Nanotechnology, Hunan University of Technology, Zhuzhou 412008, China c School of Chemistry and Chemical Engineering, Southeast University, Nanjing 210096, China d Key Laboratory of Enteric Pathogenic Microbiology (Ministry of Health), Center for Disease Prevention and Control of Jiangsu Province, Nanjing 210009, China |
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Abstract: | ![]() 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 (NH2-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. |
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Keywords: | 87.14.Gg 82.39.Pj 78.67.Bf 75.75.+a |
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