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First-principles study of high-conductance DNA sequencing with carbon nanotube electrodes

机译:碳纳米管电极高导DNA测序的第一性原理研究

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摘要

Rapid and cost-effective DNA sequencing at the single nucleotide level might be achieved by measuring a transverse electronic current as single-stranded DNA is pulled through a nanometer-sized pore. In order to enhance the electronic coupling between the nucleotides and the electrodes and hence the current signals, we employ a pair of single-walled close-ended (6,6) carbon nanotubes (CNTs) as electrodes. We then investigate the electron transport properties of nucleotides sandwiched between such electrodes by using first-principles quantum transport theory. In particular, we consider the extreme case where the separation between the electrodes is the smallest possible that still allows the DNA translocation. The benzene-like ring at the end cap of the CNT can strongly couple with the nucleobases and therefore it can both reduce conformational fluctuations and significantly improve the conductance. As such, when the electrodes are closely spaced, the nucleobases can pass through only with their base plane parallel to the plane of CNT end caps. The optimal molecular configurations, at which the nucleotides strongly couple to the CNTs, and which yield the largest transmission, are first identified. These correspond approximately to the lowest energy configurations. Then the electronic structures and the electron transport of these optimal configurations are analyzed. The typical tunneling currents are of the order of 50 nA for voltages up to 1 V. At higher bias, where resonant transport through the molecular states is possible, the current is of the order of several μA. Below 1 V, the currents associated to the different nucleotides are consistently distinguishable, with adenine having the largest current, guanine the second largest, cytosine the third and, finally, thymine the smallest. We further calculate the transmission coefficient profiles as the nucleotides are dragged along the DNA translocation path and investigate the effects of configurational variations. Based on these results, we propose a DNA sequencing protocol combining three possible data analysis strategies.
机译:在单核苷酸水平上拉出纳米大小的孔时,可以通过测量横向电流来实现在单核苷酸水平上快速,经济高效的DNA测序。为了增强核苷酸与电极之间的电子耦合,从而增强电流信号,我们采用一对单壁封闭式(6,6)碳纳米管(CNT)作为电极。然后,我们使用第一原理量子传输理论研究夹在这种电极之间的核苷酸的电子传输特性。特别地,我们考虑极端情况,其中电极之间的间隔是最小的,仍然允许DNA易位。 CNT端盖上的苯样环可以与核碱基牢固偶联,因此,它既可以减少构象波动,又可以大大提高电导率。这样,当电极紧密间隔时,核碱基只能以其底平面平行于CNT端盖的平面穿过。首先确定最佳的分子构型,在该构型下核苷酸与CNT强力偶联,并产生最大的透射率。这些大约对应于最低能量配置。然后分析了这些最佳构型的电子结构和电子传输。对于高达1 V的电压,典型的隧穿电流约为50 nA。在更高的偏置下,可能通过分子态进行共振传输,电流约为数μA。低于1 V,始终可以区分与不同核苷酸相关的电流,腺嘌呤的电流最大,鸟嘌呤的电流第二大,胞嘧啶的电流第三,最后是胸腺嘧啶的电流最小。当核苷酸沿着DNA易位路径拖动时,我们进一步计算了传输系数分布,并研究了构型变异的影响。基于这些结果,我们提出了结合三种可能的数据分析策略的DNA测序方案。

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