首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Single-step electronic detection of femtomolar DNA by target-induced strand displacement in an electrode-bound duplex
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Single-step electronic detection of femtomolar DNA by target-induced strand displacement in an electrode-bound duplex

机译:通过电极诱导的双链中靶标诱导的链置换对飞毛虫DNA进行单步电子检测

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摘要

We report a signal-on, electronic DNA (E-DNA) sensor that is label-free and achieves a subpicomolar detection limit. The sensor, which is based on a target-induced strand displacement mechanism, is composed of a "capture probe" attached by its 5' terminus to a gold electrode and a 5' methylene blue-modified "signaling probe" that is complementary at both its 3' and 5' termini to the capture probe. In the absence of target, hybridization between the capture and signaling probes minimizes contact between the methylene blue and electrode surface, limiting the observed redox current. Target hybridization displaces the 5' end of the signaling probe, generating a short, flexible single-stranded DNA element and producing up to a 7-fold increase in redox current. The observed signal gain is sufficient to achieve a demonstrated (not extrapolated) detection limit of 400 fM, which is among the best reported for single-step electronic DNA detection. Moreover, because sensor fabrication is straightforward, the approach appears to provide a ready alternative to the more cumbersome femtomolar electrochemical assays described to date.
机译:我们报告了一种无标记的信号式电子DNA(E-DNA)传感器,并达到了亚皮摩尔的检测极限。该传感器基于靶标引起的链位移机制,由“捕获探针”(通过其5'末端连接到金电极)和5'亚甲基蓝修饰的“信号探针”组成,两者互补其3'和5'末端连接到捕获探针。在没有靶标的情况下,捕获探针和信号探针之间的杂交可最大程度地减少亚甲基蓝与电极表面之间的接触,从而限制观察到的氧化还原电流。靶标杂交取代了信号探针的5'端,产生了一个短而灵活的单链DNA元件,并使氧化还原电流增加了7倍。观察到的信号增益足以达到400 fM的已证明(未推断)检测极限,这是单步电子DNA检测报告的最好结果之一。而且,因为传感器的制造是直接的,所以该方法似乎为迄今为止描述的更麻烦的飞摩尔电化学测定提供了现成的替代方法。

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