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Yielding Elastic Tethers Stabilize Robust Cell Adhesion
Many bacteria and eukaryotic cells express adhesive proteins at the end of tethers that elongate reversibly at constant or near constant force, which we refer to as yielding elasticity. Here we address the function of yielding elastic adhesive tethers with Escherichia coli bacteria as a model for ce...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256016/ https://www.ncbi.nlm.nih.gov/pubmed/25473833 http://dx.doi.org/10.1371/journal.pcbi.1003971 |
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author | Whitfield, Matt J. Luo, Jonathon P. Thomas, Wendy E. |
author_facet | Whitfield, Matt J. Luo, Jonathon P. Thomas, Wendy E. |
author_sort | Whitfield, Matt J. |
collection | PubMed |
description | Many bacteria and eukaryotic cells express adhesive proteins at the end of tethers that elongate reversibly at constant or near constant force, which we refer to as yielding elasticity. Here we address the function of yielding elastic adhesive tethers with Escherichia coli bacteria as a model for cell adhesion, using a combination of experiments and simulations. The adhesive bond kinetics and tether elasticity was modeled in the simulations with realistic biophysical models that were fit to new and previously published single molecule force spectroscopy data. The simulations were validated by comparison to experiments measuring the adhesive behavior of E. coli in flowing fluid. Analysis of the simulations demonstrated that yielding elasticity is required for the bacteria to remain bound in high and variable flow conditions, because it allows the force to be distributed evenly between multiple bonds. In contrast, strain-hardening and linear elastic tethers concentrate force on the most vulnerable bonds, which leads to failure of the entire adhesive contact. Load distribution is especially important to noncovalent receptor-ligand bonds, because they become exponentially shorter lived at higher force above a critical force, even if they form catch bonds. The advantage of yielding is likely to extend to any blood cells or pathogens adhering in flow, or to any situation where bonds are stretched unequally due to surface roughness, unequal native bond lengths, or conditions that act to unzip the bonds. |
format | Online Article Text |
id | pubmed-4256016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42560162014-12-11 Yielding Elastic Tethers Stabilize Robust Cell Adhesion Whitfield, Matt J. Luo, Jonathon P. Thomas, Wendy E. PLoS Comput Biol Research Article Many bacteria and eukaryotic cells express adhesive proteins at the end of tethers that elongate reversibly at constant or near constant force, which we refer to as yielding elasticity. Here we address the function of yielding elastic adhesive tethers with Escherichia coli bacteria as a model for cell adhesion, using a combination of experiments and simulations. The adhesive bond kinetics and tether elasticity was modeled in the simulations with realistic biophysical models that were fit to new and previously published single molecule force spectroscopy data. The simulations were validated by comparison to experiments measuring the adhesive behavior of E. coli in flowing fluid. Analysis of the simulations demonstrated that yielding elasticity is required for the bacteria to remain bound in high and variable flow conditions, because it allows the force to be distributed evenly between multiple bonds. In contrast, strain-hardening and linear elastic tethers concentrate force on the most vulnerable bonds, which leads to failure of the entire adhesive contact. Load distribution is especially important to noncovalent receptor-ligand bonds, because they become exponentially shorter lived at higher force above a critical force, even if they form catch bonds. The advantage of yielding is likely to extend to any blood cells or pathogens adhering in flow, or to any situation where bonds are stretched unequally due to surface roughness, unequal native bond lengths, or conditions that act to unzip the bonds. Public Library of Science 2014-12-04 /pmc/articles/PMC4256016/ /pubmed/25473833 http://dx.doi.org/10.1371/journal.pcbi.1003971 Text en © 2014 Whitfield et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Whitfield, Matt J. Luo, Jonathon P. Thomas, Wendy E. Yielding Elastic Tethers Stabilize Robust Cell Adhesion |
title | Yielding Elastic Tethers Stabilize Robust Cell Adhesion |
title_full | Yielding Elastic Tethers Stabilize Robust Cell Adhesion |
title_fullStr | Yielding Elastic Tethers Stabilize Robust Cell Adhesion |
title_full_unstemmed | Yielding Elastic Tethers Stabilize Robust Cell Adhesion |
title_short | Yielding Elastic Tethers Stabilize Robust Cell Adhesion |
title_sort | yielding elastic tethers stabilize robust cell adhesion |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256016/ https://www.ncbi.nlm.nih.gov/pubmed/25473833 http://dx.doi.org/10.1371/journal.pcbi.1003971 |
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