Piezoelectric immunosensor for direct and rapid detection of staphylococcal enterotoxin A (SEA) at the ng level

被引:58
作者
Salmain, Michele [1 ,2 ]
Ghasemi, Mahsa [1 ,2 ]
Boujday, Souhir [3 ,4 ]
Spadavecchia, Jolanda [3 ,4 ]
Techer, Clarisse [5 ]
Val, Florence [6 ]
Le Moigne, Vincent [5 ]
Gautier, Michel [5 ]
Briandet, Romain [7 ]
Pradier, Claire-Marie [3 ,4 ]
机构
[1] Chim ParisTech, Lab Charles Friedel, F-75005 Paris, France
[2] CNRS, UMR 7223, F-75005 Paris, France
[3] Univ Paris 06, UPMC, Lab Reactivite Surface, F-75005 Paris, France
[4] CNRS, UMR 7197, F-75005 Paris, France
[5] INRA Agrocampus Ouest, UMR Sci & Technol Lait & Oeuf 1253, Microbiol Lab, F-35042 Rennes, France
[6] Univ Rennes 1, INRA Agrocampus Ouest, UMR BiO3P 1099, F-35042 Rennes, France
[7] INRA, UMR MICALIS 1319, F-91300 Massy, France
关键词
Staphylococcal enterotoxin A; Immunosensor; Quartz crystal microbalance; Polyclonal antibody; Pathogenic toxin; QUARTZ-CRYSTAL MICROBALANCE; PLASMON RESONANCE DETECTION; ANTIBODY IMMOBILIZATION; BIOSENSOR METHOD; IMMUNOASSAY; ADSORPTION; FRAGMENTS;
D O I
10.1016/j.bios.2011.08.007
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A direct, label-free immunosensor was designed for the rapid detection and quantification of staphylococcal enterotoxin A (SEA) in buffered solutions using quartz crystal microbalance with dissipation (QCM-D) as transduction method. The sensing layer including the anti-SEA antibody was constructed by chemisorption of a self-assembled monolayer of cysteamine on the gold electrodes placed over the quartz crystal sensor followed by activation of the surface amino groups with the rigid homobifunctional cross-linker 1,4-phenylene diisothiocyanate (PDITC) and covalent linking of binding protein (protein A or protein G). Four anti-SEA antibodies (two of which from commercial source) have been selected to set up the most sensitive detection device. With the optimized sensing layer, a standard curve for the direct assay of SEA was established from QCM-D responses within a working range of 50-1000 or 2000 ng ml(-1) with a detection limit of 20 ng ml(-1). The total time for analysis was 15 min. Using a sandwich type assay, the response was ca. twice higher and consequently the lowest measurable concentration dropped down to 7 ng ml(-1) for a total assay time of 25 min. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:140 / 144
页数:5
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