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Quantifying the free energy landscape between polymers and minerals
Higher organisms as well as medical and technological materials exploit mineral-polymer interactions, however, mechanistic understanding of these interactions is poorly constrained. Dynamic force spectroscopy can probe the free energy landscape of interacting bonds, but interpretations are challenge...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561072/ https://www.ncbi.nlm.nih.gov/pubmed/28819212 http://dx.doi.org/10.1038/s41598-017-09041-3 |
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author | Sand, K. K. Friddle, R. W. DeYoreo, J. J. |
author_facet | Sand, K. K. Friddle, R. W. DeYoreo, J. J. |
author_sort | Sand, K. K. |
collection | PubMed |
description | Higher organisms as well as medical and technological materials exploit mineral-polymer interactions, however, mechanistic understanding of these interactions is poorly constrained. Dynamic force spectroscopy can probe the free energy landscape of interacting bonds, but interpretations are challenged by the complex mechanical behavior of polymers. Here we restate the difficulties inherent to applying DFS to polymer-linked adhesion and present an approach to gain quantitative insight into polymer-mineral binding. |
format | Online Article Text |
id | pubmed-5561072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55610722017-08-18 Quantifying the free energy landscape between polymers and minerals Sand, K. K. Friddle, R. W. DeYoreo, J. J. Sci Rep Article Higher organisms as well as medical and technological materials exploit mineral-polymer interactions, however, mechanistic understanding of these interactions is poorly constrained. Dynamic force spectroscopy can probe the free energy landscape of interacting bonds, but interpretations are challenged by the complex mechanical behavior of polymers. Here we restate the difficulties inherent to applying DFS to polymer-linked adhesion and present an approach to gain quantitative insight into polymer-mineral binding. Nature Publishing Group UK 2017-08-17 /pmc/articles/PMC5561072/ /pubmed/28819212 http://dx.doi.org/10.1038/s41598-017-09041-3 Text en © The Author(s) 2017 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sand, K. K. Friddle, R. W. DeYoreo, J. J. Quantifying the free energy landscape between polymers and minerals |
title | Quantifying the free energy landscape between polymers and minerals |
title_full | Quantifying the free energy landscape between polymers and minerals |
title_fullStr | Quantifying the free energy landscape between polymers and minerals |
title_full_unstemmed | Quantifying the free energy landscape between polymers and minerals |
title_short | Quantifying the free energy landscape between polymers and minerals |
title_sort | quantifying the free energy landscape between polymers and minerals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561072/ https://www.ncbi.nlm.nih.gov/pubmed/28819212 http://dx.doi.org/10.1038/s41598-017-09041-3 |
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