Enhancing Antibodies' Binding Capacity through Oriented Functionalization of Plasmonic Surfaces.

IgG biosensor metal enhanced fluorescence plasmonic surface surface functionalization

Journal

Nanomaterials (Basel, Switzerland)
ISSN: 2079-4991
Titre abrégé: Nanomaterials (Basel)
Pays: Switzerland
ID NLM: 101610216

Informations de publication

Date de publication:
05 Oct 2021
Historique:
received: 09 08 2021
revised: 27 09 2021
accepted: 30 09 2021
entrez: 23 10 2021
pubmed: 24 10 2021
medline: 24 10 2021
Statut: epublish

Résumé

Protein A has long been used in different research fields due to its ability to specifically recognize immunoglobulins (Ig). The protein derived from Staphylococcus aureus binds Ig through the Fc region of the antibody, showing its strongest binding in immunoglobulin G (IgG), making it the most used protein in its purification and detection. The research presented here integrates, for the first time, protein A to a silicon surface patterned with gold nanoparticles for the oriented binding of IgG. The signal detection is conveyed through a metal enhanced fluorescence (MEF) system. Orienting immunoglobulins allows the exposition of the fragment antigen-binding (Fab) region for the binding to its antigen, substantially increasing the binding capacity per antibody immobilized. Antibodies orientation is of crucial importance in many diagnostics devices, particularly when either component is in limited quantities.

Identifiants

pubmed: 34685056
pii: nano11102620
doi: 10.3390/nano11102620
pmc: PMC8538552
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Maria Laura Coluccio (ML)

BioNEM Laboratory and Nanotechnology Research Center, Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro, 88100 Catanzaro, Italy.

Fabiana Grillo (F)

Department of Chemistry, University of Leicester, Leicester LE1 7RH, UK.

Valentina Onesto (V)

Institute of Nanotechnology, National Research Council (CNR-NANOTEC), Campus Ecotekne, via Monteroni, 73100 Lecce, Italy.

Virginia Garo (V)

Department of Health Science, University "Magna Graecia" of Catanzaro, 88100 Catanzaro, Italy.

Cinzia Scala (C)

Department of Health Science, University "Magna Graecia" of Catanzaro, 88100 Catanzaro, Italy.

Paola Cuzzola (P)

BioNEM Laboratory and Nanotechnology Research Center, Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro, 88100 Catanzaro, Italy.

Michela Calfa (M)

BioNEM Laboratory and Nanotechnology Research Center, Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro, 88100 Catanzaro, Italy.

Patrizio Candeloro (P)

BioNEM Laboratory and Nanotechnology Research Center, Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro, 88100 Catanzaro, Italy.

Francesco Gentile (F)

BioNEM Laboratory and Nanotechnology Research Center, Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro, 88100 Catanzaro, Italy.

Sergey Piletsky (S)

Department of Chemistry, University of Leicester, Leicester LE1 7RH, UK.

Natalia Malara (N)

BioNEM Laboratory and Nanotechnology Research Center, Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro, 88100 Catanzaro, Italy.

Classifications MeSH