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Self-organization of waves and pulse trains by molecular motors in cellular protrusions

Actin-based cellular protrusions are an ubiquitous feature of cells, performing a variety of critical functions ranging from cell-cell communication to cell motility. The formation and maintenance of these protrusions relies on the transport of proteins via myosin motors, to the protrusion tip. Whil...

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Autores principales: Yochelis, A., Ebrahim, S., Millis, B., Cui, R., Kachar, B., Naoz, M., Gov, N. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558574/
https://www.ncbi.nlm.nih.gov/pubmed/26335545
http://dx.doi.org/10.1038/srep13521
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author Yochelis, A.
Ebrahim, S.
Millis, B.
Cui, R.
Kachar, B.
Naoz, M.
Gov, N. S.
author_facet Yochelis, A.
Ebrahim, S.
Millis, B.
Cui, R.
Kachar, B.
Naoz, M.
Gov, N. S.
author_sort Yochelis, A.
collection PubMed
description Actin-based cellular protrusions are an ubiquitous feature of cells, performing a variety of critical functions ranging from cell-cell communication to cell motility. The formation and maintenance of these protrusions relies on the transport of proteins via myosin motors, to the protrusion tip. While tip-directed motion leads to accumulation of motors (and their molecular cargo) at the protrusion tip, it is observed that motors also form rearward moving, periodic and isolated aggregates. The origins and mechanisms of these aggregates, and whether they are important for the recycling of motors, remain open puzzles. Motivated by novel myosin-XV experiments, a mass conserving reaction-diffusion-advection model is proposed. The model incorporates a non-linear cooperative interaction between motors, which converts them between an active and an inactive state. Specifically, the type of aggregate formed (traveling waves or pulse-trains) is linked to the kinetics of motors at the protrusion tip which is introduced by a boundary condition. These pattern selection mechanisms are found not only to qualitatively agree with empirical observations but open new vistas to the transport phenomena by molecular motors in general.
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spelling pubmed-45585742015-09-11 Self-organization of waves and pulse trains by molecular motors in cellular protrusions Yochelis, A. Ebrahim, S. Millis, B. Cui, R. Kachar, B. Naoz, M. Gov, N. S. Sci Rep Article Actin-based cellular protrusions are an ubiquitous feature of cells, performing a variety of critical functions ranging from cell-cell communication to cell motility. The formation and maintenance of these protrusions relies on the transport of proteins via myosin motors, to the protrusion tip. While tip-directed motion leads to accumulation of motors (and their molecular cargo) at the protrusion tip, it is observed that motors also form rearward moving, periodic and isolated aggregates. The origins and mechanisms of these aggregates, and whether they are important for the recycling of motors, remain open puzzles. Motivated by novel myosin-XV experiments, a mass conserving reaction-diffusion-advection model is proposed. The model incorporates a non-linear cooperative interaction between motors, which converts them between an active and an inactive state. Specifically, the type of aggregate formed (traveling waves or pulse-trains) is linked to the kinetics of motors at the protrusion tip which is introduced by a boundary condition. These pattern selection mechanisms are found not only to qualitatively agree with empirical observations but open new vistas to the transport phenomena by molecular motors in general. Nature Publishing Group 2015-09-03 /pmc/articles/PMC4558574/ /pubmed/26335545 http://dx.doi.org/10.1038/srep13521 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yochelis, A.
Ebrahim, S.
Millis, B.
Cui, R.
Kachar, B.
Naoz, M.
Gov, N. S.
Self-organization of waves and pulse trains by molecular motors in cellular protrusions
title Self-organization of waves and pulse trains by molecular motors in cellular protrusions
title_full Self-organization of waves and pulse trains by molecular motors in cellular protrusions
title_fullStr Self-organization of waves and pulse trains by molecular motors in cellular protrusions
title_full_unstemmed Self-organization of waves and pulse trains by molecular motors in cellular protrusions
title_short Self-organization of waves and pulse trains by molecular motors in cellular protrusions
title_sort self-organization of waves and pulse trains by molecular motors in cellular protrusions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558574/
https://www.ncbi.nlm.nih.gov/pubmed/26335545
http://dx.doi.org/10.1038/srep13521
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