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Aminoethyl substitution enhances the self-assembly properties of an aminocellulose as a potential archaeological wood consolidant
The 6-deoxy-6-aminocelluloses—or “aminocelluloses”—are a class of synthetic natural cellulose derivatives which are mostly aqueous soluble and have excellent film-forming properties. Recent studies have connected these properties at the molecular level with protein-like self-associative behaviour fo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7701074/ https://www.ncbi.nlm.nih.gov/pubmed/32844285 http://dx.doi.org/10.1007/s00249-020-01451-y |
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author | Wakefield, Jennifer M. K. Hampe, Robert Gillis, Richard B. Sitterli, Agnes Adams, Gary G. Kutzke, Hartmut Heinze, Thomas Harding, Stephen E. |
author_facet | Wakefield, Jennifer M. K. Hampe, Robert Gillis, Richard B. Sitterli, Agnes Adams, Gary G. Kutzke, Hartmut Heinze, Thomas Harding, Stephen E. |
author_sort | Wakefield, Jennifer M. K. |
collection | PubMed |
description | The 6-deoxy-6-aminocelluloses—or “aminocelluloses”—are a class of synthetic natural cellulose derivatives which are mostly aqueous soluble and have excellent film-forming properties. Recent studies have connected these properties at the molecular level with protein-like self-associative behaviour for a range of aminocelluloses including a 6-deoxy-6-(ω-aminoethyl) aminocellulose AEA-1 with the association being a two-stage process—a reversible oligomerisation followed by further (semi-reversible) aggregation into larger structures. Here, we synthesise and compare a new 6-deoxy-6-(ω-aminoethyl) aminocellulose AEA-1′ with different degree of substitution with one with further alkyl derivatisation, namely 6-deoxy-6-(ω-hydroxyethyl) aminocellulose HEA-1′. As with AEA-1, sedimentation velocity and sedimentation equilibrium in the analytical ultracentrifuge still show a two-stage process for both AEA-1′ and HEA-1′, with the latter giving higher molar masses. The consequences of these properties for use as consolidants for archaeological wood are considered. |
format | Online Article Text |
id | pubmed-7701074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-77010742020-12-03 Aminoethyl substitution enhances the self-assembly properties of an aminocellulose as a potential archaeological wood consolidant Wakefield, Jennifer M. K. Hampe, Robert Gillis, Richard B. Sitterli, Agnes Adams, Gary G. Kutzke, Hartmut Heinze, Thomas Harding, Stephen E. Eur Biophys J Original Article The 6-deoxy-6-aminocelluloses—or “aminocelluloses”—are a class of synthetic natural cellulose derivatives which are mostly aqueous soluble and have excellent film-forming properties. Recent studies have connected these properties at the molecular level with protein-like self-associative behaviour for a range of aminocelluloses including a 6-deoxy-6-(ω-aminoethyl) aminocellulose AEA-1 with the association being a two-stage process—a reversible oligomerisation followed by further (semi-reversible) aggregation into larger structures. Here, we synthesise and compare a new 6-deoxy-6-(ω-aminoethyl) aminocellulose AEA-1′ with different degree of substitution with one with further alkyl derivatisation, namely 6-deoxy-6-(ω-hydroxyethyl) aminocellulose HEA-1′. As with AEA-1, sedimentation velocity and sedimentation equilibrium in the analytical ultracentrifuge still show a two-stage process for both AEA-1′ and HEA-1′, with the latter giving higher molar masses. The consequences of these properties for use as consolidants for archaeological wood are considered. Springer International Publishing 2020-08-25 2020 /pmc/articles/PMC7701074/ /pubmed/32844285 http://dx.doi.org/10.1007/s00249-020-01451-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article Wakefield, Jennifer M. K. Hampe, Robert Gillis, Richard B. Sitterli, Agnes Adams, Gary G. Kutzke, Hartmut Heinze, Thomas Harding, Stephen E. Aminoethyl substitution enhances the self-assembly properties of an aminocellulose as a potential archaeological wood consolidant |
title | Aminoethyl substitution enhances the self-assembly properties of an aminocellulose as a potential archaeological wood consolidant |
title_full | Aminoethyl substitution enhances the self-assembly properties of an aminocellulose as a potential archaeological wood consolidant |
title_fullStr | Aminoethyl substitution enhances the self-assembly properties of an aminocellulose as a potential archaeological wood consolidant |
title_full_unstemmed | Aminoethyl substitution enhances the self-assembly properties of an aminocellulose as a potential archaeological wood consolidant |
title_short | Aminoethyl substitution enhances the self-assembly properties of an aminocellulose as a potential archaeological wood consolidant |
title_sort | aminoethyl substitution enhances the self-assembly properties of an aminocellulose as a potential archaeological wood consolidant |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7701074/ https://www.ncbi.nlm.nih.gov/pubmed/32844285 http://dx.doi.org/10.1007/s00249-020-01451-y |
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