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Self-consistent field theory for the interactions between keratin intermediate filaments
BACKGROUND: Keratins are important structural proteins found in skin, hair and nails. Keratin Intermediate Filaments are major components of corneocytes, nonviable horny cells of the Stratum Corneum, the outermost layer of skin. It is considered that interactions between unstructured domains of Kera...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848802/ https://www.ncbi.nlm.nih.gov/pubmed/24007681 http://dx.doi.org/10.1186/2046-1682-6-12 |
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author | Akinshina, Anna Jambon-Puillet, Etienne Warren, Patrick B Noro, Massimo G |
author_facet | Akinshina, Anna Jambon-Puillet, Etienne Warren, Patrick B Noro, Massimo G |
author_sort | Akinshina, Anna |
collection | PubMed |
description | BACKGROUND: Keratins are important structural proteins found in skin, hair and nails. Keratin Intermediate Filaments are major components of corneocytes, nonviable horny cells of the Stratum Corneum, the outermost layer of skin. It is considered that interactions between unstructured domains of Keratin Intermediate Filaments are the key factor in maintaining the elasticity of the skin. RESULTS: We have developed a model for the interactions between keratin intermediate filaments based on self-consistent field theory. The intermediate filaments are represented by charged surfaces, and the disordered terminal domains of the keratins are represented by charged heteropolymers grafted to these surfaces. We estimate the system is close to a charge compensation point where the heteropolymer grafting density is matched to the surface charge density. Using a protein model with amino acid resolution for the terminal domains, we find that the terminal chains can mediate a weak attraction between the keratin surfaces. The origin of the attraction is a combination of bridging and electrostatics. The attraction disappears when the system moves away from the charge compensation point, or when excess small ions and/or NMF-representing free amino acids are added. CONCLUSIONS: These results are in concordance with experimental observations, and support the idea that the interaction between keratin filaments, and ultimately in part the elastic properties of the keratin-containing tissue, is controlled by a combination of the physico-chemical properties of the disordered terminal domains and the composition of the medium in the inter-filament region. |
format | Online Article Text |
id | pubmed-3848802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38488022013-12-06 Self-consistent field theory for the interactions between keratin intermediate filaments Akinshina, Anna Jambon-Puillet, Etienne Warren, Patrick B Noro, Massimo G BMC Biophys Research Article BACKGROUND: Keratins are important structural proteins found in skin, hair and nails. Keratin Intermediate Filaments are major components of corneocytes, nonviable horny cells of the Stratum Corneum, the outermost layer of skin. It is considered that interactions between unstructured domains of Keratin Intermediate Filaments are the key factor in maintaining the elasticity of the skin. RESULTS: We have developed a model for the interactions between keratin intermediate filaments based on self-consistent field theory. The intermediate filaments are represented by charged surfaces, and the disordered terminal domains of the keratins are represented by charged heteropolymers grafted to these surfaces. We estimate the system is close to a charge compensation point where the heteropolymer grafting density is matched to the surface charge density. Using a protein model with amino acid resolution for the terminal domains, we find that the terminal chains can mediate a weak attraction between the keratin surfaces. The origin of the attraction is a combination of bridging and electrostatics. The attraction disappears when the system moves away from the charge compensation point, or when excess small ions and/or NMF-representing free amino acids are added. CONCLUSIONS: These results are in concordance with experimental observations, and support the idea that the interaction between keratin filaments, and ultimately in part the elastic properties of the keratin-containing tissue, is controlled by a combination of the physico-chemical properties of the disordered terminal domains and the composition of the medium in the inter-filament region. BioMed Central 2013-09-05 /pmc/articles/PMC3848802/ /pubmed/24007681 http://dx.doi.org/10.1186/2046-1682-6-12 Text en Copyright © 2013 Akinshina et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License(http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Akinshina, Anna Jambon-Puillet, Etienne Warren, Patrick B Noro, Massimo G Self-consistent field theory for the interactions between keratin intermediate filaments |
title | Self-consistent field theory for the interactions between keratin intermediate filaments |
title_full | Self-consistent field theory for the interactions between keratin intermediate filaments |
title_fullStr | Self-consistent field theory for the interactions between keratin intermediate filaments |
title_full_unstemmed | Self-consistent field theory for the interactions between keratin intermediate filaments |
title_short | Self-consistent field theory for the interactions between keratin intermediate filaments |
title_sort | self-consistent field theory for the interactions between keratin intermediate filaments |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848802/ https://www.ncbi.nlm.nih.gov/pubmed/24007681 http://dx.doi.org/10.1186/2046-1682-6-12 |
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