首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Electrochemical detection of β-amyloid peptides on electrode covered with N-terminus-specific antibody based on electrocatalytic O_2 reduction by Aβ(1-16)-heme-modified gold nanoparticles
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Electrochemical detection of β-amyloid peptides on electrode covered with N-terminus-specific antibody based on electrocatalytic O_2 reduction by Aβ(1-16)-heme-modified gold nanoparticles

机译:基于Aβ(1-16)-血红素修饰的金纳米粒子对O_2的电催化还原作用,对N末端特异性抗体覆盖的电极上的β-淀粉样肽进行电化学检测

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摘要

β-Amyloid (Aβ) peptides are believed to be important for the diagnosis and prognosis of Alzheimer's disease (AD) serving as reliable molecular biomarkers. In this work, we reported a simple and sensitive electrochemical strategy for the detection of total Aβ peptides using gold nanoparticles modified with Aβ(1-16)-heme (denoted as Aβ(1-16)-heme-AuNPs). Monoclonal antibody (mAb) specific to the common N-terminus of Aβ was immobilized onto gold electrode for the capture of Aβ(1-16)-heme-AuNPs. The anchored Aβ(1-16)-heme-AuNPs showed strong electrocatalytic O_2 reduction. Pre-incubation of the mAb-covered electrode with native Aβ decreased the amount of Aβ(1-16)-heme-AuNPs immobilized onto the electrode, resulting in the decrease of the reduction current of O_2 to H_2O_2. The competitive assay is sensitive and selective to Aβ peptides. The voltammetric responses were found to be proportional to the concentrations of Aβ ranging from 0.02 to 1.50nM, and a detection limit of 10pM was achieved. To demonstrate the viability of the method for the analysis of Aβ in real sample, artificial cerebrospinal fluid (aCSF) containing Aβ(1-40), Aβ(1-42) and Aβ(1-16) was tested. We believe that the method would offer a useful means for quantifying Aβ in a biological matrix, and be valuable in the design of new types of electrochemical biosensors for the detection of peptides and proteins.
机译:据信β-淀粉样蛋白(Aβ)肽对于作为可靠的分子生物标记物的阿尔茨海默氏病(AD)的诊断和预后很重要。在这项工作中,我们报告了一种简单而灵敏的电化学策略,用于使用经Aβ(1-16)-血红素修饰的金纳米颗粒(表示为Aβ(1-16)-血红素-AuNPs)检测总Aβ肽。将对Aβ常见N端特异的单克隆抗体(mAb)固定在金电极上,以捕获Aβ(1-16)-血红素-AuNPs。锚定的Aβ(1-16)-血红素-AuNPs具有很强的电催化O_2还原能力。用天然Aβ对被mAb覆盖的电极进行预孵育会减少固定在电极上的Aβ(1-16)-血红素-AuNPs的数量,从而降低O_2还原为H_2O_2的电流。竞争性测定法对Aβ肽敏感且具有选择性。发现伏安响应与Aβ的浓度成正比,范围为0.02至1.50nM,检出限为10pM。为了证明实际样品中Aβ分析方法的可行性,测试了包含Aβ(1-40),Aβ(1-42)和Aβ(1-16)的人工脑脊液(aCSF)。我们相信,该方法将为定量生物基质中的Aβ提供有用的手段,并且在设计用于检测肽和蛋白质的新型电化学生物传感器中具有重要价值。

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