Grafting of a peptide probe for Prostate-Specific Antigen detection using diazonium electroreduction and click chemistry

被引:33
|
作者
Strzeminska, I. [1 ]
Fanchine, S. Sainte Rose [1 ]
Anquetin, G. [1 ]
Reisberg, S. [1 ]
Noel, V. [1 ]
Pham, M. C. [1 ]
Piro, B. [1 ]
机构
[1] Univ Paris Diderot, Sorbonne Paris Cite, ITODYS, UMR CNRS 7086, 15 Rue JA de Baif, F-75205 Paris 13, France
来源
关键词
Electrochemical peptide sensor; Label-free detection; Prostate-specific Antigen (PSA); Click chemistry; Diazonium salts; ELECTROCHEMICAL IMMUNOSENSORS; TERMINAL ALKYNES; PSA DETECTION; BIOSENSOR; LABEL; GOLD; IMMUNOASSAY; AMPLIFICATION; DEPOSITION; FERROCENE;
D O I
10.1016/j.bios.2016.02.060
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The main objective of this work was to validate a label-free electrochemical method of protein detection using peptides as capture probes. As a proof-of-concept, we used a 7 amino acids sequence (HSSKLQL) specific for Prostate Specific Antigen. We investigated various electrografting conditions of two anilines (2-[(4-aminophenyl)sulfanyl]-8-hydroxy-1,4-naphthoquinone and 4-azidoaniline) further converted in situ into their corresponding diazonium salts on glassy carbon electrodes. It was demonstrated that the best method to obtain a mixed layer is the simultaneous electroreduction of the two diazonium salts. 4-azidoaniline was used to covalently immobilize the ethynyl-functionalized peptide probe by click coupling, and the hydroxynaphthoquinone derivative plays the role of electrochemical transducer of the peptide-protein recognition. The proteolytic activity of PSA towards a small peptide substrate carrying streptavidin at its distal end was also investigated to design an original sensing architecture leading to a reagentless, label free, and "signal-on" PSA sensor. Without optimization, the limit of quantification can be estimated in the nM to pM range. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:131 / 137
页数:7
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