State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering. Southeast University, Nanjing 210096, China.
Anal Biochem. 2010 Oct 1;405(1):141-3. doi: 10.1016/j.ab.2010.05.016. Epub 2010 May 25.
A high-throughput and cost-effective single-nucleotide polymorphism (SNP) genotyping method based on a gold magnetic nanoparticle (GMNP) array with dual-color hybridization has been designed. Biotinylated single-strand polymerase chain reaction (PCR) products containing the SNP locus were captured by the GMNPs that were coated with streptavidin. The GMNP array was fabricated by immobilizing single-stranded DNA (ssDNA)-GMNP complexes onto a glass slide using a magnetic field, and SNPs were identified with dual-color fluorescence hybridization. Three different SNP loci from 24 samples were genotyped successfully using this platform. This procedure allows the user to directly analyze the bead fluorescence to determine the SNP genotype, and it eliminates the need for background subtraction for signal determination. This method also bypasses tedious PCR purification and concentration procedures, and it facilitates large-scale SNP studies by using a method that is highly sensitive, simple, labor-saving, and potentially automatable.
设计了一种基于金磁纳米粒子(GMNP)阵列的高通量、低成本的单核苷酸多态性(SNP)基因分型方法,该方法基于双色杂交。用链霉亲和素包被的 GMNP 捕获含有 SNP 位点的生物素化单链聚合酶链反应(PCR)产物。GMNP 阵列是通过将单链 DNA(ssDNA)-GMNP 复合物固定在载玻片上来制备的,并用双色荧光杂交来识别 SNPs。该平台成功地对 24 个样本中的 3 个不同的 SNP 位点进行了基因分型。该方法允许用户直接分析珠粒荧光来确定 SNP 基因型,并且消除了信号确定时的背景扣除的需要。该方法还绕过了繁琐的 PCR 纯化和浓缩程序,并且通过使用高度敏感、简单、省力且具有潜在自动化能力的方法,促进了大规模 SNP 研究。