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Hydrodynamic instabilities provide a generic route to spontaneous biomimetic oscillations in chemomechanically active filaments

Non-equilibrium processes which convert chemical energy into mechanical motion enable the motility of organisms. Bundles of inextensible filaments driven by energy transduction of molecular motors form essential components of micron-scale motility engines like cilia and flagella. The mimicry of cili...

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Autores principales: Laskar, Abhrajit, Singh, Rajeev, Ghose, Somdeb, Jayaraman, Gayathri, Kumar, P. B. Sunil, Adhikari, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678140/
https://www.ncbi.nlm.nih.gov/pubmed/23752497
http://dx.doi.org/10.1038/srep01964
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author Laskar, Abhrajit
Singh, Rajeev
Ghose, Somdeb
Jayaraman, Gayathri
Kumar, P. B. Sunil
Adhikari, R.
author_facet Laskar, Abhrajit
Singh, Rajeev
Ghose, Somdeb
Jayaraman, Gayathri
Kumar, P. B. Sunil
Adhikari, R.
author_sort Laskar, Abhrajit
collection PubMed
description Non-equilibrium processes which convert chemical energy into mechanical motion enable the motility of organisms. Bundles of inextensible filaments driven by energy transduction of molecular motors form essential components of micron-scale motility engines like cilia and flagella. The mimicry of cilia-like motion in recent experiments on synthetic active filaments supports the idea that generic physical mechanisms may be sufficient to generate such motion. Here we show, theoretically, that the competition between the destabilising effect of hydrodynamic interactions induced by force-free and torque-free chemomechanically active flows, and the stabilising effect of nonlinear elasticity, provides a generic route to spontaneous oscillations in active filaments. These oscillations, reminiscent of prokaryotic and eukaryotic flagellar motion, are obtained without having to invoke structural complexity or biochemical regulation. This minimality implies that biomimetic oscillations, previously observed only in complex bundles of active filaments, can be replicated in simple chains of generic chemomechanically active beads.
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spelling pubmed-36781402013-06-11 Hydrodynamic instabilities provide a generic route to spontaneous biomimetic oscillations in chemomechanically active filaments Laskar, Abhrajit Singh, Rajeev Ghose, Somdeb Jayaraman, Gayathri Kumar, P. B. Sunil Adhikari, R. Sci Rep Article Non-equilibrium processes which convert chemical energy into mechanical motion enable the motility of organisms. Bundles of inextensible filaments driven by energy transduction of molecular motors form essential components of micron-scale motility engines like cilia and flagella. The mimicry of cilia-like motion in recent experiments on synthetic active filaments supports the idea that generic physical mechanisms may be sufficient to generate such motion. Here we show, theoretically, that the competition between the destabilising effect of hydrodynamic interactions induced by force-free and torque-free chemomechanically active flows, and the stabilising effect of nonlinear elasticity, provides a generic route to spontaneous oscillations in active filaments. These oscillations, reminiscent of prokaryotic and eukaryotic flagellar motion, are obtained without having to invoke structural complexity or biochemical regulation. This minimality implies that biomimetic oscillations, previously observed only in complex bundles of active filaments, can be replicated in simple chains of generic chemomechanically active beads. Nature Publishing Group 2013-06-11 /pmc/articles/PMC3678140/ /pubmed/23752497 http://dx.doi.org/10.1038/srep01964 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Article
Laskar, Abhrajit
Singh, Rajeev
Ghose, Somdeb
Jayaraman, Gayathri
Kumar, P. B. Sunil
Adhikari, R.
Hydrodynamic instabilities provide a generic route to spontaneous biomimetic oscillations in chemomechanically active filaments
title Hydrodynamic instabilities provide a generic route to spontaneous biomimetic oscillations in chemomechanically active filaments
title_full Hydrodynamic instabilities provide a generic route to spontaneous biomimetic oscillations in chemomechanically active filaments
title_fullStr Hydrodynamic instabilities provide a generic route to spontaneous biomimetic oscillations in chemomechanically active filaments
title_full_unstemmed Hydrodynamic instabilities provide a generic route to spontaneous biomimetic oscillations in chemomechanically active filaments
title_short Hydrodynamic instabilities provide a generic route to spontaneous biomimetic oscillations in chemomechanically active filaments
title_sort hydrodynamic instabilities provide a generic route to spontaneous biomimetic oscillations in chemomechanically active filaments
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678140/
https://www.ncbi.nlm.nih.gov/pubmed/23752497
http://dx.doi.org/10.1038/srep01964
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