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基于银纳米粒子网络的信号放大的淀粉样β寡聚物的电化学检测。

Electrochemical Detection of Amyloid-β Oligomers Based on the Signal Amplification of a Network of Silver Nanoparticles.

机构信息

Henan Province of Key Laboratory of New Optoelectronic Functional Materials, College of Chemistry and Chemical Engineering, Anyang Normal University , Anyang, Henan 455000, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2016 Aug 3;8(30):19303-11. doi: 10.1021/acsami.6b05423. Epub 2016 Jul 22.

Abstract

Amyloid-β oligomers (AβOs) are the most important toxic species in the brain of Alzheimer's disease (AD) patient. AβOs, therefore, are considered reliable molecular biomarkers for the diagnosis of AD. Herein, we reported a simple and sensitive electrochemical method for the selective detection of AβOs using silver nanoparticles (AgNPs) as the redox reporters and PrP(95-110), an AβOs-specific binding peptide, as the receptor. Specifically, adamantine (Ad)-labeled PrP(95-110), denoted as Ad-PrP(95-110), induced the aggregation and color change of AgNPs and the follow-up formation of a network of Ad-PrP(95-110)-AgNPs. Then, Ad-PrP(95-110)-AgNPs were anchored onto a β-cyclodextrin (β-CD)-covered electrode surface through the host-guest interaction between Ad and β-CD, thus producing an amplified electrochemical signal through the solid-state Ag/AgCl reaction by the AgNPs. In the presence of AβOs, Ad-PrP(95-110) interacted specifically with the AβOs, thus losing the capability to bind AgNPs and to induce the formation of an AgNPs-based network on the electrode surface. Consequently, the electrochemical signal decreased with an increase in the concentration of AβOs in the range of 20 pM to 100 nM. The biosensor had a detection limit of 8 pM and showed no response to amyloid-β monomers (AβMs) and fibrils (AβFs). On the basis of the well-defined and amplified electrochemical signal of the AgNPs-based network architecture, these results should be valuable for the design of novel electrochemical biosensors by marrying specific receptors.

摘要

淀粉样β寡聚体(AβOs)是阿尔茨海默病(AD)患者大脑中最重要的毒性物质。因此,AβOs 被认为是 AD 诊断的可靠分子生物标志物。在此,我们报道了一种简单灵敏的电化学方法,用于使用银纳米粒子(AgNPs)作为氧化还原报告分子和 PrP(95-110),一种 AβOs 特异性结合肽作为受体,选择性检测 AβOs。具体来说,金刚烷(Ad)标记的 PrP(95-110),表示为 Ad-PrP(95-110),诱导 AgNPs 的聚集和颜色变化,以及后续形成 Ad-PrP(95-110)-AgNPs 的网络。然后,Ad-PrP(95-110)-AgNPs 通过 Ad 和 β-CD 之间的主客体相互作用被锚定在β-环糊精(β-CD)覆盖的电极表面上,从而通过 AgNPs 的固态 Ag/AgCl 反应产生放大的电化学信号。在存在 AβOs 的情况下,Ad-PrP(95-110)与 AβOs 特异性相互作用,从而失去与 AgNPs 结合并在电极表面上诱导 AgNPs 基网络形成的能力。因此,随着 AβOs 浓度在 20 pM 至 100 nM 范围内的增加,电化学信号降低。该生物传感器的检测限为 8 pM,对淀粉样β单体(AβMs)和纤维(AβFs)没有响应。基于 AgNPs 基网络结构的定义明确和放大的电化学信号,这些结果对于通过结合特异性受体设计新型电化学生物传感器应该是有价值的。

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