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Toward hybridization assays without PCR using universal nanoamplicons

机译:无需使用通用纳米扩增子进行PCR的杂交测定

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An innovative scheme for signal amplification using random tetramer-modified gold nanoparticles, termed “nanoamplicons,” has been developed for hybridization assay without PCR. Large numbers of nanoamplicons could be integrated onto one target, providing much greater amplification than the larger nanoparticles usually adopted. Using M13mp18 single-strand DNA as a target, this concept is shown to be a feasible approach to detecting 0.17 amol L−1 DNA without target amplification, based on microgravimetric detection of the adsorption of the probe–target–nanoamplicons complex via thiol–gold binding. To our knowledge, this method has a sensitivity that is close to that of PCR and superior to those of nanoparticle-based methods reported previously. Additionally, this novel nanoamplicon could be prepared in the same way and used for all diagnostic tests; such universality would make the nanoamplicons highly advantageous for the generalization and standardization of bioassays, and when applying this new technology in clinical laboratories.
机译:已经开发了一种使用随机四聚体修饰的金纳米颗粒进行信号放大的创新方案,称为“纳米扩增子”,用于无需PCR的杂交测定。可以将大量的纳米扩增子整合到一个靶标上,比通常采用的较大的纳米颗粒提供更大的扩增。以M13mp18单链DNA为靶标,该概念被证明是一种在不进行靶标扩增的情况下检测0.17 amol L-1 DNA的可行方法,它是基于探针-靶标-纳米扩增子复合物吸附的微重力检测通过硫醇-金结合。据我们所知,这种方法的灵敏度接近于PCR,并且优于先前报道的基于纳米颗粒的方法。此外,可以用相同的方法制备这种新颖的纳米扩增子,并用于所有诊断测试。这种通用性将使纳米安瓿对于生物测定的一般化和标准化以及在临床实验室中应用这项新技术时非常有利。

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