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Sequence specific electronic conduction through polyion-stabilized double-stranded DNA in nanoscale break junctions

机译:纳米级断裂连接中通过聚离子稳定的双链DNA进行的序列特异性电子传导

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摘要

This paper presents a study of sequence specific electronic conduction through short (15-base- pair) double-stranded (ds) DNA molecules, measured by immobilizing 3\u27-thiol-derivatized DNAs in nanometre scale gaps between gold electrodes. The polycation spermidine was used to stabilize the ds-DNA structure, allowing electrical measurements to be performed in a dry state. For specific sequences, the conductivity was observed to scale with the surface density of immobilized DNA, which can be controlled by the buffer concentration. A series of 15-base DNA oligonucleotide pairs, in which the centre sequence of five base pairs was changed from G: C to A: T pairs, has been studied. The conductivity per molecule is observed to decrease exponentially with the number of adjacent A: T pairs replacing G: C pairs, consistent with a barrier at the A: T sites. Conductance-based devices for short DNA sequences could provide sensing approaches with direct electrical readout, as well as label-free detection.
机译:本文介绍了通过短(15个碱基对)双链(ds)DNA分子进行序列特异性电子传导的研究,该方法通过将3 \ u27-硫醇衍生的DNA固定在金电极之间的纳米级间隙中进行测量。聚阳离子亚精胺用于稳定ds-DNA结构,允许在干燥状态下进行电测量。对于特定序列,观察到电导率与固定的DNA的表面密度成比例,该密度可由缓冲液浓度控制。已经研究了一系列15个碱基的DNA寡核苷酸对,其中5个碱基对的中心序列从G:C变为A:T。观察到每个分子的电导率随着取代A:T对的相邻A:T对的数量呈指数下降,这与A:T位点的势垒一致。用于短DNA序列的基于电导的设备可以提供具有直接电读数以及无标记检测的传感方法。

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