首页> 美国卫生研究院文献>Sensors (Basel Switzerland) >Development of an Antigen-DNAzyme Based Probe for a Direct Antibody-Antigen Assay Using the Intrinsic DNAzyme Activity of a Daunomycin Aptamer
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Development of an Antigen-DNAzyme Based Probe for a Direct Antibody-Antigen Assay Using the Intrinsic DNAzyme Activity of a Daunomycin Aptamer

机译:使用道诺霉素适体的内在DNAzyme活性直接抗体-抗原检测基于抗原-DNAzyme的探针的开发。

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摘要

G-Quadruplex (G-4) structures are formed when G-rich DNA sequences fold into intra- or intermolecular four-stranded structures in the presence of metal ions. G-4-hemin complexes are often effective peroxidase-mimicking DNAzymes that are applied in many detection systems. This work reports the application of a G-rich daunomycin-specific aptamer for the development of an antibody-antigen detection assay. We investigated the ability of the daunomycin aptamer to efficiently catalyze the hemin-dependent peroxidase activity independent of daunomycin. A reporter probe consisting of biotinylated antigen and daunomycin aptamer coupled to streptavidin gold nanoparticles was successfully used to generate a colorimetric readout. In conclusion, the daunomycin aptamer can function as a robust alternative DNAzyme for the development of colorimetric assays.
机译:当富含G的DNA序列在金属离子存在下折叠成分子内或分子间四链结构时,就会形成G-四链体(G-4)结构。 G-4-hemin复合物通常是有效的过氧化物酶模拟DNA酶,已应用于许多检测系统中。这项工作报告了富含G的道诺霉素特异性适体在开发抗体-抗原检测测定中的应用。我们研究了道诺霉素适体有效地催化独立于道诺霉素的血红素依赖性过氧化物酶活性的能力。由生物素化抗原和道诺霉素适体与链霉亲和素金纳米颗粒偶联的报告探针已成功用于产生比色读数。总之,道诺霉素适体可作为比色测定法开发的可靠替代DNA酶。

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