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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...

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Autores principales: Pilyugina, Ekaterina, Krajina, Brad, Spakowitz, Andrew J., Schieber, Jay D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
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.
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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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