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Theoretical model of membrane protrusions driven by curved active proteins

Eukaryotic cells intrinsically change their shape, by changing the composition of their membrane and by restructuring their underlying cytoskeleton. We present here further studies and extensions of a minimal physical model, describing a closed vesicle with mobile curved membrane protein complexes....

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Autores principales: Ravid, Yoav, Penič , Samo, Mimori-Kiyosue, Yuko, Suetsugu, Shiro, Iglič, Aleš, Gov, Nir S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203436/
https://www.ncbi.nlm.nih.gov/pubmed/37228585
http://dx.doi.org/10.3389/fmolb.2023.1153420
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author Ravid, Yoav
Penič , Samo
Mimori-Kiyosue, Yuko
Suetsugu, Shiro
Iglič, Aleš
Gov, Nir S.
author_facet Ravid, Yoav
Penič , Samo
Mimori-Kiyosue, Yuko
Suetsugu, Shiro
Iglič, Aleš
Gov, Nir S.
author_sort Ravid, Yoav
collection PubMed
description Eukaryotic cells intrinsically change their shape, by changing the composition of their membrane and by restructuring their underlying cytoskeleton. We present here further studies and extensions of a minimal physical model, describing a closed vesicle with mobile curved membrane protein complexes. The cytoskeletal forces describe the protrusive force due to actin polymerization which is recruited to the membrane by the curved protein complexes. We characterize the phase diagrams of this model, as function of the magnitude of the active forces, nearest-neighbor protein interactions and the proteins’ spontaneous curvature. It was previously shown that this model can explain the formation of lamellipodia-like flat protrusions, and here we explore the regimes where the model can also give rise to filopodia-like tubular protrusions. We extend the simulation with curved components of both convex and concave species, where we find the formation of complex ruffled clusters, as well as internalized invaginations that resemble the process of endocytosis and macropinocytosis. We alter the force model representing the cytoskeleton to simulate the effects of bundled instead of branched structure, resulting in shapes which resemble filopodia.
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spelling pubmed-102034362023-05-24 Theoretical model of membrane protrusions driven by curved active proteins Ravid, Yoav Penič , Samo Mimori-Kiyosue, Yuko Suetsugu, Shiro Iglič, Aleš Gov, Nir S. Front Mol Biosci Molecular Biosciences Eukaryotic cells intrinsically change their shape, by changing the composition of their membrane and by restructuring their underlying cytoskeleton. We present here further studies and extensions of a minimal physical model, describing a closed vesicle with mobile curved membrane protein complexes. The cytoskeletal forces describe the protrusive force due to actin polymerization which is recruited to the membrane by the curved protein complexes. We characterize the phase diagrams of this model, as function of the magnitude of the active forces, nearest-neighbor protein interactions and the proteins’ spontaneous curvature. It was previously shown that this model can explain the formation of lamellipodia-like flat protrusions, and here we explore the regimes where the model can also give rise to filopodia-like tubular protrusions. We extend the simulation with curved components of both convex and concave species, where we find the formation of complex ruffled clusters, as well as internalized invaginations that resemble the process of endocytosis and macropinocytosis. We alter the force model representing the cytoskeleton to simulate the effects of bundled instead of branched structure, resulting in shapes which resemble filopodia. Frontiers Media S.A. 2023-05-09 /pmc/articles/PMC10203436/ /pubmed/37228585 http://dx.doi.org/10.3389/fmolb.2023.1153420 Text en Copyright © 2023 Ravid, Penič , Mimori-Kiyosue, Suetsugu, Iglič and Gov. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Biosciences
Ravid, Yoav
Penič , Samo
Mimori-Kiyosue, Yuko
Suetsugu, Shiro
Iglič, Aleš
Gov, Nir S.
Theoretical model of membrane protrusions driven by curved active proteins
title Theoretical model of membrane protrusions driven by curved active proteins
title_full Theoretical model of membrane protrusions driven by curved active proteins
title_fullStr Theoretical model of membrane protrusions driven by curved active proteins
title_full_unstemmed Theoretical model of membrane protrusions driven by curved active proteins
title_short Theoretical model of membrane protrusions driven by curved active proteins
title_sort theoretical model of membrane protrusions driven by curved active proteins
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203436/
https://www.ncbi.nlm.nih.gov/pubmed/37228585
http://dx.doi.org/10.3389/fmolb.2023.1153420
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