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Impedimetric and Plasmonic Sensing of Collagen I Using a Half-Antibody-Supported, Au-Modified, Self-Assembled Monolayer System

This research presents an electrochemical immunosensor for collagen I detection using a self-assembled monolayer (SAM) of gold nanoparticles (AuNPs) and covalently immobilized half-reduced monoclonal antibody as a receptor; this allowed for the validation of the collagen I concentration through two...

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Autores principales: Gwiazda, Marcin, Bhardwaj, Sheetal K., Kijeńska-Gawrońska, Ewa, Swieszkowski, Wojciech, Sivasankaran, Unni, Kaushik, Ajeet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301786/
https://www.ncbi.nlm.nih.gov/pubmed/34356698
http://dx.doi.org/10.3390/bios11070227
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author Gwiazda, Marcin
Bhardwaj, Sheetal K.
Kijeńska-Gawrońska, Ewa
Swieszkowski, Wojciech
Sivasankaran, Unni
Kaushik, Ajeet
author_facet Gwiazda, Marcin
Bhardwaj, Sheetal K.
Kijeńska-Gawrońska, Ewa
Swieszkowski, Wojciech
Sivasankaran, Unni
Kaushik, Ajeet
author_sort Gwiazda, Marcin
collection PubMed
description This research presents an electrochemical immunosensor for collagen I detection using a self-assembled monolayer (SAM) of gold nanoparticles (AuNPs) and covalently immobilized half-reduced monoclonal antibody as a receptor; this allowed for the validation of the collagen I concentration through two different independent methods: electrochemically by Electrochemical Impedance Spectroscopy (EIS), and optically by Surface Plasmon Resonance (SPR). The high unique advantage of the proposed sensor is based on the performance of the stable covalent immobilization of the AuNPs and enzymatically reduced half-IgG collagen I antibodies, which ensured their appropriate orientation onto the sensor’s surface, good stability, and sensitivity properties. The detection of collagen type I was performed in a concentration range from 1 to 5 pg/mL. Moreover, SPR was utilized to confirm the immobilization of the monoclonal half-antibodies and sensing of collagen I versus time. Furthermore, EIS experiments revealed a limit of detection (LOD) of 0.38 pg/mL. The selectivity of the performed immunosensor was confirmed by negligible responses for BSA. The performed approach of the immunosensor is a novel, innovative attempt that enables the detection of collagen I with very high sensitivity in the range of pg/mL, which is significantly lower than the commonly used enzyme-linked immunosorbent assay (ELISA).
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spelling pubmed-83017862021-07-24 Impedimetric and Plasmonic Sensing of Collagen I Using a Half-Antibody-Supported, Au-Modified, Self-Assembled Monolayer System Gwiazda, Marcin Bhardwaj, Sheetal K. Kijeńska-Gawrońska, Ewa Swieszkowski, Wojciech Sivasankaran, Unni Kaushik, Ajeet Biosensors (Basel) Article This research presents an electrochemical immunosensor for collagen I detection using a self-assembled monolayer (SAM) of gold nanoparticles (AuNPs) and covalently immobilized half-reduced monoclonal antibody as a receptor; this allowed for the validation of the collagen I concentration through two different independent methods: electrochemically by Electrochemical Impedance Spectroscopy (EIS), and optically by Surface Plasmon Resonance (SPR). The high unique advantage of the proposed sensor is based on the performance of the stable covalent immobilization of the AuNPs and enzymatically reduced half-IgG collagen I antibodies, which ensured their appropriate orientation onto the sensor’s surface, good stability, and sensitivity properties. The detection of collagen type I was performed in a concentration range from 1 to 5 pg/mL. Moreover, SPR was utilized to confirm the immobilization of the monoclonal half-antibodies and sensing of collagen I versus time. Furthermore, EIS experiments revealed a limit of detection (LOD) of 0.38 pg/mL. The selectivity of the performed immunosensor was confirmed by negligible responses for BSA. The performed approach of the immunosensor is a novel, innovative attempt that enables the detection of collagen I with very high sensitivity in the range of pg/mL, which is significantly lower than the commonly used enzyme-linked immunosorbent assay (ELISA). MDPI 2021-07-08 /pmc/articles/PMC8301786/ /pubmed/34356698 http://dx.doi.org/10.3390/bios11070227 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gwiazda, Marcin
Bhardwaj, Sheetal K.
Kijeńska-Gawrońska, Ewa
Swieszkowski, Wojciech
Sivasankaran, Unni
Kaushik, Ajeet
Impedimetric and Plasmonic Sensing of Collagen I Using a Half-Antibody-Supported, Au-Modified, Self-Assembled Monolayer System
title Impedimetric and Plasmonic Sensing of Collagen I Using a Half-Antibody-Supported, Au-Modified, Self-Assembled Monolayer System
title_full Impedimetric and Plasmonic Sensing of Collagen I Using a Half-Antibody-Supported, Au-Modified, Self-Assembled Monolayer System
title_fullStr Impedimetric and Plasmonic Sensing of Collagen I Using a Half-Antibody-Supported, Au-Modified, Self-Assembled Monolayer System
title_full_unstemmed Impedimetric and Plasmonic Sensing of Collagen I Using a Half-Antibody-Supported, Au-Modified, Self-Assembled Monolayer System
title_short Impedimetric and Plasmonic Sensing of Collagen I Using a Half-Antibody-Supported, Au-Modified, Self-Assembled Monolayer System
title_sort impedimetric and plasmonic sensing of collagen i using a half-antibody-supported, au-modified, self-assembled monolayer system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301786/
https://www.ncbi.nlm.nih.gov/pubmed/34356698
http://dx.doi.org/10.3390/bios11070227
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