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High-Throughput Quantitative Screening of Peroxidase-Mimicking DNAzymes on a Microarray by Using Electrochemical Detection

机译:高通量定量筛选过氧化物酶模拟DNA酶的电化学检测。

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Some guanine-rich DNA sequences, which are called DNAzymes, can adopt G-quadruplex structures and exhibit peroxidase activity by binding with hemin. Although known DNAzymes show less activity than horseradish peroxidase, they have the potential to be widely used for the detection of target molecules in enzyme-linked immunosorbent assays if sequences that exhibit higher activity can be identified. However, techniques for achieving this have not yet been described. Therefore, we compared the DNAzyme activities of more than 1000 novelistically designed sequences with that of the original DNAzyme by using an electrochemical detection system on a 12K DNA microarray platform. To the best of our knowledge, this is the first description of an array-based assessment of peroxidase activity of G-quadruplexhemin complexes. By using this novel assay system, more than 200 different mutants were found that had significantly higher activities than the original DNAzyme sequence. This microarray-based DNAzyme evaluation system is useful for identifying highly active new DNAzymes that might have potential as tools for developing DNA-based biosensors with aptamers.
机译:一些富含鸟嘌呤的DNA序列(称为DNA酶)可以采用G-四链体结构,并通过与血红素结合而表现出过氧化物酶活性。尽管已知的脱氧核糖核酸酶比辣根过氧化物酶具有较低的活性,但如果可以鉴定出表现出较高活性的序列,它们有可能被广泛用于酶联免疫吸附测定中的目标分子检测。然而,尚未描述用于实现此目的的技术。因此,通过在12K DNA微阵列平台上使用电化学检测系统,我们比较了1000多个新颖设计的序列与原始DNAzyme的DNAzyme活性。据我们所知,这是对基于阵列的G-四链体血红素复合物过氧化物酶活性评估的首次描述。通过使用这种新颖的测定系统,发现了200多种不同的突变体,其活性明显高于原始DNAzyme序列。这种基于微阵列的DNAzyme评估系统可用于鉴定高度活跃的新型DNAzyme,这些新的DNAzyme可能具有开发带有适体的基于DNA的生物传感器的潜力。

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