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Buckling a Semiflexible Polymer Chain under Compression
Instability and structural transitions arise in many important problems involving dynamics at molecular length scales. Buckling of an elastic rod under a compressive load offers a useful general picture of such a transition. However, the existing theoretical description of buckling is applicable in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432112/ https://www.ncbi.nlm.nih.gov/pubmed/30970780 http://dx.doi.org/10.3390/polym9030099 |
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author | Pilyugina, Ekaterina Krajina, Brad Spakowitz, Andrew J. Schieber, Jay D. |
author_facet | Pilyugina, Ekaterina Krajina, Brad Spakowitz, Andrew J. Schieber, Jay D. |
author_sort | Pilyugina, Ekaterina |
collection | PubMed |
description | Instability and structural transitions arise in many important problems involving dynamics at molecular length scales. Buckling of an elastic rod under a compressive load offers a useful general picture of such a transition. However, the existing theoretical description of buckling is applicable in the load response of macroscopic structures, only when fluctuations can be neglected, whereas membranes, polymer brushes, filaments, and macromolecular chains undergo considerable Brownian fluctuations. We analyze here the buckling of a fluctuating semiflexible polymer experiencing a compressive load. Previous works rely on approximations to the polymer statistics, resulting in a range of predictions for the buckling transition that disagree on whether fluctuations elevate or depress the critical buckling force. In contrast, our theory exploits exact results for the statistical behavior of the worm-like chain model yielding unambiguous predictions about the buckling conditions and nature of the buckling transition. We find that a fluctuating polymer under compressive load requires a larger force to buckle than an elastic rod in the absence of fluctuations. The nature of the buckling transition exhibits a marked change from being distinctly second order in the absence of fluctuations to being a more gradual, compliant transition in the presence of fluctuations. We analyze the thermodynamic contributions throughout the buckling transition to demonstrate that the chain entropy favors the extended state over the buckled state, providing a thermodynamic justification of the elevated buckling force. |
format | Online Article Text |
id | pubmed-6432112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64321122019-04-02 Buckling a Semiflexible Polymer Chain under Compression Pilyugina, Ekaterina Krajina, Brad Spakowitz, Andrew J. Schieber, Jay D. Polymers (Basel) Article Instability and structural transitions arise in many important problems involving dynamics at molecular length scales. Buckling of an elastic rod under a compressive load offers a useful general picture of such a transition. However, the existing theoretical description of buckling is applicable in the load response of macroscopic structures, only when fluctuations can be neglected, whereas membranes, polymer brushes, filaments, and macromolecular chains undergo considerable Brownian fluctuations. We analyze here the buckling of a fluctuating semiflexible polymer experiencing a compressive load. Previous works rely on approximations to the polymer statistics, resulting in a range of predictions for the buckling transition that disagree on whether fluctuations elevate or depress the critical buckling force. In contrast, our theory exploits exact results for the statistical behavior of the worm-like chain model yielding unambiguous predictions about the buckling conditions and nature of the buckling transition. We find that a fluctuating polymer under compressive load requires a larger force to buckle than an elastic rod in the absence of fluctuations. The nature of the buckling transition exhibits a marked change from being distinctly second order in the absence of fluctuations to being a more gradual, compliant transition in the presence of fluctuations. We analyze the thermodynamic contributions throughout the buckling transition to demonstrate that the chain entropy favors the extended state over the buckled state, providing a thermodynamic justification of the elevated buckling force. MDPI 2017-03-11 /pmc/articles/PMC6432112/ /pubmed/30970780 http://dx.doi.org/10.3390/polym9030099 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pilyugina, Ekaterina Krajina, Brad Spakowitz, Andrew J. Schieber, Jay D. Buckling a Semiflexible Polymer Chain under Compression |
title | Buckling a Semiflexible Polymer Chain under Compression |
title_full | Buckling a Semiflexible Polymer Chain under Compression |
title_fullStr | Buckling a Semiflexible Polymer Chain under Compression |
title_full_unstemmed | Buckling a Semiflexible Polymer Chain under Compression |
title_short | Buckling a Semiflexible Polymer Chain under Compression |
title_sort | buckling a semiflexible polymer chain under compression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432112/ https://www.ncbi.nlm.nih.gov/pubmed/30970780 http://dx.doi.org/10.3390/polym9030099 |
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