Esteves-Villanueva Jose O, Trzeciakiewicz Hanna, Martic Sanela
Department of Chemistry, Oakland University, 2200 North Squirrel Road, Rochester, MI, USA48309.
Analyst. 2014 Jun 7;139(11):2823-31. doi: 10.1039/c4an00204k.
A protein-based electrochemical biosensor was developed for detection of tau protein aimed towards electrochemically sensing misfolding proteins. The electrochemical assay monitors tau-tau binding and misfolding during the early stage of tau oligomerization. Electrochemical impedance spectroscopy was used to detect the binding event between solution tau protein and immobilized tau protein (tau-Au), acting as a recognition element. The charge transfer resistance (Rct) of tau-Au was 2.9 ± 0.6 kΩ. Subsequent tau binding to tau-Au decreased the Rct to 0.3 ± 0.1 kΩ (90 ± 3% decrease) upon formation of a tau-tau-Au interface. A linear relationship between the Rct and the solution tau concentration was observed from 0.2 to 1.0 μM. The Rct decrease was attributed to an enhanced charge permeability of the tau-tau-Au surface to a redox probe Fe(CN)6. The electrochemical and surface characterization data suggested conformational and electrostatic changes induced by tau-tau binding. The protein-based electrochemical platform was highly selective for tau protein over bovine serum albumin and allowed for a rapid sample analysis. The protein-based interface was selective for a non-phosphorylated tau441 isoform over the paired-helical filaments of tau, which were composed of phosphorylated and truncated tau isoforms. The electrochemical approach may find application in screening of the early onset of neurodegeneration and aggregation inhibitors.
开发了一种基于蛋白质的电化学生物传感器,用于检测tau蛋白,旨在对错误折叠的蛋白质进行电化学传感。该电化学检测方法监测tau寡聚化早期阶段的tau-tau结合和错误折叠。采用电化学阻抗谱检测溶液中的tau蛋白与作为识别元件的固定化tau蛋白(tau-Au)之间的结合事件。tau-Au的电荷转移电阻(Rct)为2.9±0.6 kΩ。随后,tau与tau-Au结合,形成tau-tau-Au界面后,Rct降至0.3±0.1 kΩ(降低90±3%)。在0.2至1.0 μM范围内,观察到Rct与溶液中tau浓度之间存在线性关系。Rct的降低归因于tau-tau-Au表面对氧化还原探针Fe(CN)6的电荷渗透性增强。电化学和表面表征数据表明tau-tau结合引起了构象和静电变化。该基于蛋白质的电化学平台对tau蛋白的选择性高于牛血清白蛋白,并允许快速进行样品分析。该基于蛋白质的界面对于非磷酸化的tau441异构体比对由磷酸化和截短的tau异构体组成的tau双螺旋丝具有更高的选择性。这种电化学方法可能在神经退行性变早期发作的筛查和聚集抑制剂的筛选中得到应用。