Rapid Antibody Selection Using Surface Plasmon Resonance for High-Speed and Sensitive Hazelnut Lateral Flow Prototypes
Autor: | Maria G. E. G. Bremer, Georgina M. S. Ross, Michel W. F. Nielen, Aart van Amerongen, Jan H. Wichers |
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Jazyk: | angličtina |
Předmět: |
Carbon nanoparticles
Carbon Nanoparticles Monsteradministratie & Coördinatie lcsh:Biotechnology Clinical Biochemistry 02 engineering and technology 01 natural sciences Article BU Dierbehandelingsmiddelen BU Veterinary Drugs Matrix (chemical analysis) Corylus Limit of Detection lcsh:TP248.13-248.65 Surface plasmon resonance Humans Food allergens VLAG Immunoassay Chromatography Smartphone detection biology Chemistry Ligand binding assay 010401 analytical chemistry Organic Chemistry Antibodies Monoclonal General Medicine High-speed lateral flow immunoassay Antigens Plant 021001 nanoscience & nanotechnology Antibody selection Organische Chemie Carbon 0104 chemical sciences Test line BBP Bioconversion Smartphone app biology.protein Nanoparticles Food allergen Antibody 0210 nano-technology Food Hypersensitivity |
Zdroj: | Biosensors, 8(4) Biosensors Volume 8 Issue 4 Biosensors, Vol 8, Iss 4, p 130 (2018) Biosensors 8 (2018) 4 |
ISSN: | 2079-6374 |
DOI: | 10.3390/bios8040130 |
Popis: | Lateral Flow Immunoassays (LFIAs) allow for rapid, low-cost, screening of many biomolecules such as food allergens. Despite being classified as rapid tests, many LFIAs take 10–20 min to complete. For a really high-speed LFIA, it is necessary to assess antibody association kinetics. By using a label-free optical technique such as Surface Plasmon Resonance (SPR), it is possible to screen crude monoclonal antibody (mAb) preparations for their association rates against a target. Herein, we describe an SPR-based method for screening and selecting crude anti-hazelnut antibodies based on their relative association rates, cross reactivity and sandwich pairing capabilities, for subsequent application in a rapid ligand binding assay. Thanks to the SPR selection process, only the fast mAb (F-50-6B12) and the slow (S-50-5H9) mAb needed purification for labelling with carbon nanoparticles to exploit high-speed LFIA prototypes. The kinetics observed in SPR were reflected in LFIA, with the test line appearing within 30 s, almost two times faster when F-50-6B12 was used, compared with S-50-5H9. Additionally, the LFIAs have demonstrated their future applicability to real life samples by detecting hazelnut in the sub-ppm range in a cookie matrix. Finally, these LFIAs not only provide a qualitative result when read visually, but also generate semi-quantitative data when exploiting freely downloadable smartphone apps. |
Databáze: | OpenAIRE |
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