An Electrochemical Immunosensor Based on a Self-Assembled Monolayer Modified Electrode for Label-Free Detection of α-Synuclein

This research demonstrated the development of a simple, cost-effective, and label-free immunosensor for the detection of α-synuclein (α-Syn) based on a cystamine (CYS) self-assembled monolayer (SAM) decorated fluorine-doped tin oxide (FTO) electrode. CYS-SAM was formed onto the FTO electrode by the...

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Veröffentlicht in:Sensors (Basel, Switzerland) Switzerland), 2020-01, Vol.20 (3), p.617
Hauptverfasser: Ge, Chuang-Ye, Rahman, Md Mahbubur, Zhang, Wei, Lopa, Nasrin Siraj, Jin, Lei, Yoon, Sujin, Jang, Hohyon, Xu, Guang-Ri, Kim, Whangi
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Sprache:eng
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Zusammenfassung:This research demonstrated the development of a simple, cost-effective, and label-free immunosensor for the detection of α-synuclein (α-Syn) based on a cystamine (CYS) self-assembled monolayer (SAM) decorated fluorine-doped tin oxide (FTO) electrode. CYS-SAM was formed onto the FTO electrode by the adsorption of CYS molecules through the head sulfur groups. The free amine (-NH ) groups at the tail of the CYS-SAM enabled the immobilization of anti-α-Syn-antibody, which concurrently allowed the formation of immunocomplex by covalent bonding with α-Syn-antigen. The variation of the concentrations of the attached α-Syn at the immunosensor probe induced the alternation of the current and the charge transfer resistance ( ) for the redox response of [Fe(CN) ] , which displayed a linear dynamic range from 10 to 1000 ng/mL with a low detection limit ( / = ) of ca. 3.62 and 1.13 ng/mL in differential pulse voltammetry (DPV) and electrochemical impedance spectra (EIS) measurements, respectively. The immunosensor displayed good reproducibility, anti-interference ability, and good recoveries of α-Syn detection in diluted human serum samples. The proposed immunosensor is a promising platform to detect α-Syn for the early diagnose of Parkinson's disease, which can be extended for the determination of other biologically important biomarkers.
ISSN:1424-8220
1424-8220
DOI:10.3390/s20030617