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Fabricating three-dimensional hydrogel oligonucleotide microarrays to detect single nucleotide polymorph isms

机译:制作三维水凝胶寡核苷酸微阵列以检测单核苷酸多态性

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摘要

Here, a three-dimensional (3D) oligonucleotide microarray-based fluorescent assay has been developed for single nucleotide polymorphisms (SNPs) and allele frequency determination. The 3D oligonucleotide microarray is fabricated on a home-made polyacrylamide hydrogel microarray which is generated by UV light photopolymerization of tiny acrylamide monomer droplets on a PEG terminated glass slide. After activation by glutaraldehyde (GA), the polyacrylamide hydrogel is able to react with NH2-modified oligonucleotides with high efficiency to generate a high signal-to-background ratio without the conventional blocking step. We demonstrate that the assay is able to detect complimentary 25 mer oligonucleotide target (fragment of a tumor suppressor gene P53) down to 100 pM and SNP with true-to-false ratios (the ratio of fluorescence signal from perfect matched DNA strands to that from the one-base mismatched DNA strands) above 20. Taking advantage of the high specificity of the assay, allele frequency as low as 2% can be accurately determined.
机译:在这里,已开发出基于三维(3D)寡核苷酸微阵列的荧光测定法,用于单核苷酸多态性(SNP)和等位基因频率测定。 3D寡核苷酸微阵列是在自制的聚丙烯酰胺水凝胶微阵列上制造的,该阵列是通过将PEG封端的载玻片上的微小丙烯酰胺单体液滴进行紫外线光聚合而生成的。通过戊二醛(GA)激活后,聚丙烯酰胺水凝胶能够与NH2修饰的寡核苷酸高效反应,以产生高信噪比,而无需常规阻断步骤。我们证明了该检测方法能够检测到互补的25 mer寡核苷酸靶标(肿瘤抑制基因P53的片段),其低至100 pM和SNP的真假比(完美匹配的DNA链与荧光信号的比值) 20条以上的单碱基错配DNA链)。利用测定的高特异性,可以精确确定低至2%的等位基因频率。

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