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Bioluminescent detection of zearalenone using recombinant peptidomimetic Gaussia luciferase fusion protein.
Peltomaa, Riikka; Fikacek, Sabrina; Benito-Peña, Elena; Barderas, Rodrigo; Head, Trajen; Deo, Sapna; Daunert, Sylvia; Moreno-Bondi, María C.
Afiliação
  • Peltomaa R; Department of Analytical Chemistry, Faculty of Chemistry, Complutense University, Ciudad Universitaria s/n, 28040, Madrid, Spain.
  • Fikacek S; Department of Analytical Chemistry, Faculty of Chemistry, Complutense University, Ciudad Universitaria s/n, 28040, Madrid, Spain.
  • Benito-Peña E; Department of Analytical Chemistry, Faculty of Chemistry, Complutense University, Ciudad Universitaria s/n, 28040, Madrid, Spain. elenabp@ucm.es.
  • Barderas R; Chronic Disease Programme, UFIEC, Instituto de Salud Carlos III, Ctra. Majadahonda-Pozuelo Km 2.2, 28220, Madrid, Spain.
  • Head T; Department of Biochemistry and Molecular Biology, Miller School of Medicine, University of Miami, Miami, FL, 33136, USA.
  • Deo S; Dr. JT Macdonald Foundation Biomedical Nanotechnology Institute, University of Miami, Coral Gables, FL, 33136, USA.
  • Daunert S; Department of Biochemistry and Molecular Biology, Miller School of Medicine, University of Miami, Miami, FL, 33136, USA.
  • Moreno-Bondi MC; Dr. JT Macdonald Foundation Biomedical Nanotechnology Institute, University of Miami, Coral Gables, FL, 33136, USA.
Mikrochim Acta ; 187(10): 547, 2020 09 04.
Article em En | MEDLINE | ID: mdl-32886242
ABSTRACT
The development of a bioluminescent immunosensor is reported for the determination of zearalenone (ZEA) based on a peptide mimetic identified by phage display. The peptide mimetic GW, with a peptide sequence GWWGPYGEIELL, was used to create recombinant fusion proteins with the bioluminescent Gaussia luciferase (GLuc) that were directly used as tracers for toxin detection in a competitive immunoassay without the need for secondary antibodies or further labeling. The bioluminescent sensor, based on protein G-coupled magnetic beads for antibody immobilization, enabled determination of ZEA with a detection limit of 4.2 ng mL-1 (corresponding to 420 µg kg-1 in food samples) and an IC50 value of 11.0 ng mL-1. The sensor performance was evaluated in spiked maize and wheat samples, with recoveries ranging from 87 to 106% (RSD < 20%, n = 3). Finally, the developed method was applied to the analysis of a naturally contaminated reference matrix material and good agreement with the reported concentrations was obtained.Graphical abstract.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Zearalenona / Proteínas Recombinantes de Fusão / Peptidomiméticos Tipo de estudo: Diagnostic_studies Idioma: En Revista: Mikrochim Acta Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Zearalenona / Proteínas Recombinantes de Fusão / Peptidomiméticos Tipo de estudo: Diagnostic_studies Idioma: En Revista: Mikrochim Acta Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Espanha