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Molecular Architectures for Electrocatalytic Amplification of Oligonucleotide Hybridization

机译:寡核苷酸杂交的电催化扩增的分子结构。

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In this work, we describe a new platform suitable for electrocatalytic amplification of oligonucleotide hybridization based on the use of supramolecular bioconjugates incorporating ferrocene-labeled streptavidin. Our goals were aimed at designing a biosensing platform which could support highly reproducible and stable electrocatalytic amplification with maximum efficiency. The use of nonlabeled streptavidin as an underlying layer promotes a major improvement on the characteristics of the amplified electrochemical signal. In addition, the electrocatalytic current can be easily amplified by tuning the concentration of electron donor species in solution. Because of the fact that the redox labels are bioconjugated to the DNA strands, increasing the ionic strength does not lead to the loss of redox labels. More importantly, increasing the concentration of donors only involves the magnification of the signal without implying the permeation of donors (thus reducing the efficient electrocatalysis). This approach represents a major improvement on the use of electrocatalytically amplified DNA-sensing platforms, thus overcoming any possible limitation in connection with the reproducibility and reliability of this well-established method.
机译:在这项工作中,我们描述了一个新平台,该平台适用于基于结合二茂铁标记的链霉亲和素的超分子生物共轭物的使用,对寡核苷酸杂交进行电催化扩增。我们的目标旨在设计一个生物传感平台,该平台可以以最大的效率支持高度可重复且稳定的电催化扩增。使用未标记的抗生蛋白链菌素作为基础层促进了放大的电化学信号特性的重大改进。另外,通过调节溶液中电子供体种类的浓度可以容易地放大电催化电流。由于氧化还原标记与DNA链生物偶联,因此增加离子强度不会导致氧化还原标记的丢失。更重要的是,增加供体的浓度仅涉及信号的放大,而不意味着供体的渗透(因此降低了有效的电催化作用)。这种方法代表了对使用电催化扩增的DNA传感平台的重大改进,因此克服了与该成熟方法的可重复性和可靠性相关的任何可能的限制。

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