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

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...

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Autores principales: Li, Song, Liu, Hongna, Jia, Yingying, Deng, Yan, Zhang, Liming, Lu, Zhuoxuan, He, Nongyue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493202/
https://www.ncbi.nlm.nih.gov/pubmed/23139724
http://dx.doi.org/10.7150/thno.5032
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author Li, Song
Liu, Hongna
Jia, Yingying
Deng, Yan
Zhang, Liming
Lu, Zhuoxuan
He, Nongyue
author_facet Li, Song
Liu, Hongna
Jia, Yingying
Deng, Yan
Zhang, Liming
Lu, Zhuoxuan
He, Nongyue
author_sort Li, Song
collection PubMed
description 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.
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spelling pubmed-34932022012-11-08 A Novel SNPs Detection Method Based on Gold Magnetic Nanoparticles Array and Single Base Extension Li, Song Liu, Hongna Jia, Yingying Deng, Yan Zhang, Liming Lu, Zhuoxuan He, Nongyue Theranostics Research Paper 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. Ivyspring International Publisher 2012-10-09 /pmc/articles/PMC3493202/ /pubmed/23139724 http://dx.doi.org/10.7150/thno.5032 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Li, Song
Liu, Hongna
Jia, Yingying
Deng, Yan
Zhang, Liming
Lu, Zhuoxuan
He, Nongyue
A Novel SNPs Detection Method Based on Gold Magnetic Nanoparticles Array and Single Base Extension
title A Novel SNPs Detection Method Based on Gold Magnetic Nanoparticles Array and Single Base Extension
title_full A Novel SNPs Detection Method Based on Gold Magnetic Nanoparticles Array and Single Base Extension
title_fullStr A Novel SNPs Detection Method Based on Gold Magnetic Nanoparticles Array and Single Base Extension
title_full_unstemmed A Novel SNPs Detection Method Based on Gold Magnetic Nanoparticles Array and Single Base Extension
title_short A Novel SNPs Detection Method Based on Gold Magnetic Nanoparticles Array and Single Base Extension
title_sort novel snps detection method based on gold magnetic nanoparticles array and single base extension
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493202/
https://www.ncbi.nlm.nih.gov/pubmed/23139724
http://dx.doi.org/10.7150/thno.5032
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