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碳纳米管适体传感器中的静电门控。

Electrostatic gating in carbon nanotube aptasensors.

机构信息

School of Chemical and Physical Sciences, Victoria University of Wellington, Wellington 6021, New Zealand.

Polymer Electronics Research Centre (PERC), School of Chemical Sciences, University of Auckland, 23 Symonds Street, Auckland, New Zealand.

出版信息

Nanoscale. 2016 Jul 14;8(28):13659-68. doi: 10.1039/c5nr08117c.

Abstract

Synthetic DNA aptamer receptors could boost the prospects of carbon nanotube (CNT)-based electronic biosensors if signal transduction can be understood and engineered. Here, we report CNT aptasensors for potassium ions that clearly demonstrate aptamer-induced electrostatic gating of electronic conduction. The CNT network devices were fabricated on flexible substrates via a facile solution processing route and non-covalently functionalised with potassium binding aptamers. Monotonic increases in CNT conduction were observed in response to increasing potassium ion concentration, with a level of detection as low as 10 picomolar. The signal was shown to arise from a specific aptamer-target interaction that stabilises a G-quadruplex structure, bringing high negative charge density near the CNT channel. Electrostatic gating is established via the specificity and the sign of the current response, and by observing its suppression when higher ionic strength decreases the Debye length at the CNT-water interface. Sensitivity towards potassium and selectivity against other ions is demonstrated in both resistive mode and real time transistor mode measurements. The effective device architecture presented, along with the identification of clear response signatures, should inform the development of new electronic biosensors using the growing library of aptamer receptors.

摘要

合成 DNA 适体受体如果能够理解和设计信号转导,可能会提高基于碳纳米管 (CNT) 的电子生物传感器的前景。在这里,我们报告了用于钾离子的 CNT 适体传感器,这些传感器清楚地证明了适体诱导的电子传导的静电门控。通过简便的溶液处理方法在柔性基板上制造 CNT 网络器件,并通过非共价键功能化与钾结合适体。随着钾离子浓度的增加,观察到 CNT 传导的单调增加,检测水平低至 10 皮摩尔。该信号源于一种特定的适体-靶相互作用,该相互作用稳定了 G-四链体结构,使 CNT 通道附近的高负电荷密度。静电门控是通过电流响应的特异性和符号以及观察到当较高的离子强度降低 CNT-水界面处的德拜长度时其抑制作用来建立的。在电阻模式和实时晶体管模式测量中均证明了对钾的敏感性和对其他离子的选择性。所提出的有效器件结构以及明确的响应特征的确定,应该为使用不断增长的适体受体库开发新的电子生物传感器提供信息。

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