Wang Bing-Yu, Gu Bien-Chen, Wang Gou-Jen, Yang Yuan-Han, Wu Chia-Che
Department of Mechanical Engineering, National Chung Hsing University, Taichung, Taiwan.
Graduate Institute of Biomedical Engineering, National Chung Hsing University, Taichung, Taiwan.
Front Bioeng Biotechnol. 2022 Mar 16;10:853947. doi: 10.3389/fbioe.2022.853947. eCollection 2022.
Amyloid-β(1-42) [Aβ(1-42)] oligomer accumulations are associated with physiologic alterations in the brains of individuals with Alzheimer's disease. In this study, we demonstrate that a nanostructured gold electrode with deposited gold nanoparticles, induced via electrochemical impedance spectroscopy (EIS), may be used as an Aβ(1-42) conformation biosensor for the detection of Alzheimer's disease. Monoclonal antibodies (12F4) were immobilized on self-assembled monolayers of the electrochemical sandwich immunoassay biosensor to capture Aβ(1-42) monomers and oligomers. Western blot and fluorescence microscopy analyses were performed to confirm the presence of Aβ(1-42) monomers and oligomers. EIS analysis with an equivalent circuit model was used to determine the concentrations of different Aβ(1-42) conformations in this study. We identified conformations of Aβ(1-42) monomers and Aβ(1-42) oligomers using probe antibodies (12F4) by employing EIS. indicates the sum resistance of impedance measured during Aβ(1-42) immobilization. refers to the concentration of probe antibody (12F4) binding with Aβ(1-42). The concentration of Aβ(1-42) oligomer was defined as the percentage of Aβ(1-42) aggregation . The experimental results show that the biosensor has high selectivity to differentiate Aβ(1-40) and Aβ(1-42) monomers and Aβ(1-42) oligomers and that it can detect Aβ(1-42) oligomer accurately. The linear detection range for Aβ(1-42) oligomers was between 10 pg/ml and 100 ng/ml. The limit of detection was estimated to be 113 fg/ml.
淀粉样β蛋白(1-42)[Aβ(1-42)]寡聚体聚集与阿尔茨海默病患者大脑中的生理改变有关。在本研究中,我们证明了通过电化学阻抗谱(EIS)诱导沉积金纳米颗粒的纳米结构金电极可用作检测阿尔茨海默病的Aβ(1-42)构象生物传感器。将单克隆抗体(12F4)固定在电化学夹心免疫分析生物传感器的自组装单层上,以捕获Aβ(1-42)单体和寡聚体。进行蛋白质免疫印迹和荧光显微镜分析以确认Aβ(1-42)单体和寡聚体的存在。在本研究中,使用等效电路模型的EIS分析来确定不同Aβ(1-42)构象的浓度。我们通过EIS使用探针抗体(12F4)鉴定了Aβ(1-42)单体和Aβ(1-42)寡聚体的构象。 表示在Aβ(1-42)固定过程中测量的阻抗的总电阻。 指与Aβ(1-42)结合的探针抗体(12F4)的浓度。Aβ(1-42)寡聚体的浓度定义为Aβ(1-42)聚集的百分比 。实验结果表明,该生物传感器对区分Aβ(1-40)和Aβ(1-42)单体以及Aβ(1-42)寡聚体具有高选择性,并且能够准确检测Aβ(1-42)寡聚体。Aβ(1-42)寡聚体的线性检测范围在10 pg/ml至100 ng/ml之间。检测限估计为113 fg/ml。