A protein-based electrochemical biosensor for detection of tau protein, a neurodegenerative disease biomarker

被引:65
|
作者
Esteves-Villanueva, Jose O. [1 ]
Trzeciakiewicz, Hanna [1 ]
Martic, Sanela [1 ]
机构
[1] Oakland Univ, Dept Chem, Rochester, MI 48309 USA
关键词
PAIRED HELICAL FILAMENTS; IMPEDANCE SPECTROSCOPY; NEUROFIBRILLARY TANGLES; IMMUNOSENSOR ASSAY; DNA HYBRIDIZATION; ADSORPTION; GOLD; AGGREGATION; SURFACES; PHOSPHORYLATION;
D O I
10.1039/c4an00204k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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 (R-ct) of tau-Au was 2.9 +/- 0.6 k Omega. Subsequent tau binding to tau-Au decreased the R-ct to 0.3 + 0.1 k Omega (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 mu M. The Rct decrease was attributed to an enhanced charge permeability of the tau-tau-Au surface to a redox probe [Fe(CN)(6)](3/4) . 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.
引用
收藏
页码:2823 / 2831
页数:9
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