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Mechanisms for Covalent Immobilization of Horseradish Peroxidase on Ion-Beam-Treated Polyethylene

The surface of polyethylene was modified by plasma immersion ion implantation. Structure changes including carbonization and oxidation were observed. High surface energy of the modified polyethylene was attributed to the presence of free radicals on the surface. The surface energy decay with storage...

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Autores principales: Kondyurin, Alexey V., Naseri, Pourandokht, Tilley, Jennifer M. R., Nosworthy, Neil J., Bilek, Marcela M. M., McKenzie, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820519/
https://www.ncbi.nlm.nih.gov/pubmed/24278665
http://dx.doi.org/10.6064/2012/126170
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author Kondyurin, Alexey V.
Naseri, Pourandokht
Tilley, Jennifer M. R.
Nosworthy, Neil J.
Bilek, Marcela M. M.
McKenzie, David R.
author_facet Kondyurin, Alexey V.
Naseri, Pourandokht
Tilley, Jennifer M. R.
Nosworthy, Neil J.
Bilek, Marcela M. M.
McKenzie, David R.
author_sort Kondyurin, Alexey V.
collection PubMed
description The surface of polyethylene was modified by plasma immersion ion implantation. Structure changes including carbonization and oxidation were observed. High surface energy of the modified polyethylene was attributed to the presence of free radicals on the surface. The surface energy decay with storage time after treatment was explained by a decay of the free radical concentration while the concentration of oxygen-containing groups increased with storage time. Horseradish peroxidase was covalently attached onto the modified surface by the reaction with free radicals. Appropriate blocking agents can block this reaction. All aminoacid residues can take part in the covalent attachment process, providing a universal mechanism of attachment for all proteins. The native conformation of attached protein is retained due to hydrophilic interactions in the interface region. The enzymatic activity of covalently attached protein remained high. The long-term activity of the modified layer to attach protein is explained by stabilisation of unpaired electrons in sp(2) carbon structures. A high concentration of free radicals can give multiple covalent bonds to the protein molecule and destroy the native conformation and with it the catalytic activity. The universal mechanism of protein attachment to free radicals could be extended to various methods of radiation damage of polymers.
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spelling pubmed-38205192013-11-25 Mechanisms for Covalent Immobilization of Horseradish Peroxidase on Ion-Beam-Treated Polyethylene Kondyurin, Alexey V. Naseri, Pourandokht Tilley, Jennifer M. R. Nosworthy, Neil J. Bilek, Marcela M. M. McKenzie, David R. Scientifica (Cairo) Research Article The surface of polyethylene was modified by plasma immersion ion implantation. Structure changes including carbonization and oxidation were observed. High surface energy of the modified polyethylene was attributed to the presence of free radicals on the surface. The surface energy decay with storage time after treatment was explained by a decay of the free radical concentration while the concentration of oxygen-containing groups increased with storage time. Horseradish peroxidase was covalently attached onto the modified surface by the reaction with free radicals. Appropriate blocking agents can block this reaction. All aminoacid residues can take part in the covalent attachment process, providing a universal mechanism of attachment for all proteins. The native conformation of attached protein is retained due to hydrophilic interactions in the interface region. The enzymatic activity of covalently attached protein remained high. The long-term activity of the modified layer to attach protein is explained by stabilisation of unpaired electrons in sp(2) carbon structures. A high concentration of free radicals can give multiple covalent bonds to the protein molecule and destroy the native conformation and with it the catalytic activity. The universal mechanism of protein attachment to free radicals could be extended to various methods of radiation damage of polymers. Hindawi Publishing Corporation 2012 2012-12-31 /pmc/articles/PMC3820519/ /pubmed/24278665 http://dx.doi.org/10.6064/2012/126170 Text en Copyright © 2012 Alexey V. Kondyurin et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kondyurin, Alexey V.
Naseri, Pourandokht
Tilley, Jennifer M. R.
Nosworthy, Neil J.
Bilek, Marcela M. M.
McKenzie, David R.
Mechanisms for Covalent Immobilization of Horseradish Peroxidase on Ion-Beam-Treated Polyethylene
title Mechanisms for Covalent Immobilization of Horseradish Peroxidase on Ion-Beam-Treated Polyethylene
title_full Mechanisms for Covalent Immobilization of Horseradish Peroxidase on Ion-Beam-Treated Polyethylene
title_fullStr Mechanisms for Covalent Immobilization of Horseradish Peroxidase on Ion-Beam-Treated Polyethylene
title_full_unstemmed Mechanisms for Covalent Immobilization of Horseradish Peroxidase on Ion-Beam-Treated Polyethylene
title_short Mechanisms for Covalent Immobilization of Horseradish Peroxidase on Ion-Beam-Treated Polyethylene
title_sort mechanisms for covalent immobilization of horseradish peroxidase on ion-beam-treated polyethylene
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820519/
https://www.ncbi.nlm.nih.gov/pubmed/24278665
http://dx.doi.org/10.6064/2012/126170
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