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A real-time PCR-based method for determining the surface coverage of thiol-capped oligonucleotides bound onto gold nanoparticles

机译:基于实时PCR的方法,用于确定结合在金纳米颗粒上的巯基封端的寡核苷酸的表面覆盖率

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Here we report a real-time PCR-based method for determining the surface coverage of dithiol-capped oligonucleotides bound onto gold nanoparticles alone and in tandem with antibody. The detection of gold nanoparticle-bound DNA is accomplished by targeting the oligonucleotide with primer and probe binding sites, amplification of the oligonucleotide by PCR, and real-time measurement of the fluorescence emitted during the reaction. This method offers a wide dynamic range and is not dependant on the dissociation of the oligonucleotide strands from the gold nanoparticle surface; the fluorophore is not highly quenched by the gold nanoparticles in solution during fluorescence measurements. We show that this method and a fluorescence-based method give equivalent results for determining the surface coverage of oligonucleotides bound onto 13 or 30 nm gold nanoparticles alone and in tandem with antibody. Quantifying the surface coverage of immobilized oligonucleotides on metallic nanoparticle surfaces is important for optimizing the sensitivity of gold nanoparticle-based detection methods and for better understanding the interactions between thiol-functionalized oligonucleotides and gold nanoparticles.
机译:在这里,我们报告了一种基于实时PCR的方法,用于确定结合到金纳米颗粒上并与抗体串联的二硫醇基寡核苷酸的表面覆盖率。通过与引物和探针结合位点靶向寡核苷酸,通过PCR扩增寡核苷酸以及实时测量反应过程中发出的荧光来完成金纳米颗粒结合DNA的检测。该方法提供了宽的动态范围,并且不依赖于寡核苷酸链与金纳米颗粒表面的解离。在荧光测量过程中,荧光团并未被溶液中的金纳米颗粒高度淬灭。我们表明,该方法和基于荧光的方法为确定与13或30 nm金纳米颗粒结合并与抗体结合的寡核苷酸的表面覆盖率提供了等效的结果。量化固定化寡核苷酸在金属纳米颗粒表面上的表面覆盖范围对于优化基于金纳米颗粒的检测方法的灵敏度以及更好地理解硫醇官能化寡核苷酸与金纳米颗粒之间的相互作用非常重要。

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