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电化学电流整流——一种基于新型信号放大策略的高灵敏度和选择性适配体生物传感器。

Electrochemical current rectification-a novel signal amplification strategy for highly sensitive and selective aptamer-based biosensor.

机构信息

Peter-Grünberg-Institute, PGI-8, Research Center Jülich, JARA-Fundamentals of Future Information Technology, Jülich 52425, Germany.

Peter-Grünberg-Institute, PGI-8, Research Center Jülich, JARA-Fundamentals of Future Information Technology, Jülich 52425, Germany.

出版信息

Biosens Bioelectron. 2015 Apr 15;66:62-8. doi: 10.1016/j.bios.2014.10.057. Epub 2014 Oct 29.

Abstract

Electrochemical aptamer-based (E-AB) sensors represent an emerging class of recently developed sensors. However, numerous of these sensors are limited by a low surface density of electrode-bound redox-oligonucleotides which are used as probe. Here we propose to use the concept of electrochemical current rectification (ECR) for the enhancement of the redox signal of E-AB sensors. Commonly, the probe-DNA performs a change in conformation during target binding and enables a nonrecurring charge transfer between redox-tag and electrode. In our system, the redox-tag of the probe-DNA is continuously replenished by solution-phase redox molecules. A unidirectional electron transfer from electrode via surface-linked redox-tag to the solution-phase redox molecules arises that efficiently amplifies the current response. Using this robust and straight-forward strategy, the developed sensor showed a substantial signal amplification and consequently improved sensitivity with a calculated detection limit of 114nM for ATP, which was improved by one order of magnitude compared with the amplification-free detection and superior to other previous detection results using enzymes or nanomaterials-based signal amplification. To the best of our knowledge, this is the first demonstration of an aptamer-based electrochemical biosensor involving electrochemical rectification, which can be presumably transferred to other biomedical sensor systems.

摘要

基于电化学适体的(E-AB)传感器代表了一类新兴的最近开发的传感器。然而,这些传感器中有许多受到电极结合的氧化还原寡核苷酸(用作探针)的表面密度低的限制。在这里,我们建议将电化学电流整流(ECR)的概念用于增强 E-AB 传感器的氧化还原信号。通常,在靶标结合期间,探针 DNA 会发生构象变化,并允许氧化还原标记物和电极之间发生非重复的电荷转移。在我们的系统中,探针 DNA 的氧化还原标记物通过溶液相氧化还原分子不断得到补充。从电极通过表面连接的氧化还原标记物到溶液相氧化还原分子的单向电子转移会发生,这有效地放大了电流响应。使用这种稳健且简单的策略,所开发的传感器显示出显著的信号放大,从而提高了对 ATP 的灵敏度,检测限为 114nM,与无放大检测相比提高了一个数量级,优于使用酶或基于纳米材料的信号放大的其他先前检测结果。据我们所知,这是第一个涉及电化学整流的基于适体的电化学生物传感器的演示,它可以推测转移到其他生物医学传感器系统。

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