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Steric Effects Induce Geometric Remodeling of Actin Bundles in Filopodia

Filopodia are ubiquitous fingerlike protrusions, spawned by many eukaryotic cells, to probe and interact with their environments. Polymerization dynamics of actin filaments, comprising the structural core of filopodia, largely determine their instantaneous lengths and overall lifetimes. The polymeri...

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Autores principales: Dobramysl, Ulrich, Papoian, Garegin A., Erban, Radek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939473/
https://www.ncbi.nlm.nih.gov/pubmed/27166814
http://dx.doi.org/10.1016/j.bpj.2016.03.013
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author Dobramysl, Ulrich
Papoian, Garegin A.
Erban, Radek
author_facet Dobramysl, Ulrich
Papoian, Garegin A.
Erban, Radek
author_sort Dobramysl, Ulrich
collection PubMed
description Filopodia are ubiquitous fingerlike protrusions, spawned by many eukaryotic cells, to probe and interact with their environments. Polymerization dynamics of actin filaments, comprising the structural core of filopodia, largely determine their instantaneous lengths and overall lifetimes. The polymerization reactions at the filopodial tip require transport of G-actin, which enter the filopodial tube from the filopodial base and diffuse toward the filament barbed ends near the tip. Actin filaments are mechanically coupled into a tight bundle by cross-linker proteins. Interestingly, many of these proteins are relatively short, restricting the free diffusion of cytosolic G-actin throughout the bundle and, in particular, its penetration into the bundle core. To investigate the effect of steric restrictions on G-actin diffusion by the porous structure of filopodial actin filament bundle, we used a particle-based stochastic simulation approach. We discovered that excluded volume interactions result in partial and then full collapse of central filaments in the bundle, leading to a hollowed-out structure. The latter may further collapse radially due to the activity of cross-linking proteins, hence producing conical-shaped filament bundles. Interestingly, electron microscopy experiments on mature filopodia indeed frequently reveal actin bundles that are narrow at the tip and wider at the base. Overall, our work demonstrates that excluded volume effects in the context of reaction-diffusion processes in porous networks may lead to unexpected geometric growth patterns and complicated, history-dependent dynamics of intermediate metastable configurations.
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spelling pubmed-49394732017-05-10 Steric Effects Induce Geometric Remodeling of Actin Bundles in Filopodia Dobramysl, Ulrich Papoian, Garegin A. Erban, Radek Biophys J Cell Biophysics Filopodia are ubiquitous fingerlike protrusions, spawned by many eukaryotic cells, to probe and interact with their environments. Polymerization dynamics of actin filaments, comprising the structural core of filopodia, largely determine their instantaneous lengths and overall lifetimes. The polymerization reactions at the filopodial tip require transport of G-actin, which enter the filopodial tube from the filopodial base and diffuse toward the filament barbed ends near the tip. Actin filaments are mechanically coupled into a tight bundle by cross-linker proteins. Interestingly, many of these proteins are relatively short, restricting the free diffusion of cytosolic G-actin throughout the bundle and, in particular, its penetration into the bundle core. To investigate the effect of steric restrictions on G-actin diffusion by the porous structure of filopodial actin filament bundle, we used a particle-based stochastic simulation approach. We discovered that excluded volume interactions result in partial and then full collapse of central filaments in the bundle, leading to a hollowed-out structure. The latter may further collapse radially due to the activity of cross-linking proteins, hence producing conical-shaped filament bundles. Interestingly, electron microscopy experiments on mature filopodia indeed frequently reveal actin bundles that are narrow at the tip and wider at the base. Overall, our work demonstrates that excluded volume effects in the context of reaction-diffusion processes in porous networks may lead to unexpected geometric growth patterns and complicated, history-dependent dynamics of intermediate metastable configurations. The Biophysical Society 2016-05-10 2016-05-10 /pmc/articles/PMC4939473/ /pubmed/27166814 http://dx.doi.org/10.1016/j.bpj.2016.03.013 Text en © 2016 Biophysical Society. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Cell Biophysics
Dobramysl, Ulrich
Papoian, Garegin A.
Erban, Radek
Steric Effects Induce Geometric Remodeling of Actin Bundles in Filopodia
title Steric Effects Induce Geometric Remodeling of Actin Bundles in Filopodia
title_full Steric Effects Induce Geometric Remodeling of Actin Bundles in Filopodia
title_fullStr Steric Effects Induce Geometric Remodeling of Actin Bundles in Filopodia
title_full_unstemmed Steric Effects Induce Geometric Remodeling of Actin Bundles in Filopodia
title_short Steric Effects Induce Geometric Remodeling of Actin Bundles in Filopodia
title_sort steric effects induce geometric remodeling of actin bundles in filopodia
topic Cell Biophysics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939473/
https://www.ncbi.nlm.nih.gov/pubmed/27166814
http://dx.doi.org/10.1016/j.bpj.2016.03.013
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