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Organization at criticality enables processing of time‐varying signals by receptor networks

How cells utilize surface receptors for chemoreception is a recurrent question spanning between physics and biology over the past few decades. However, the dynamical mechanism for processing time‐varying signals is still unclear. Using dynamical systems formalism to describe criticality in non‐equil...

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Detalles Bibliográficos
Autores principales: Stanoev, Angel, Nandan, Akhilesh P, Koseska, Aneta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036718/
https://www.ncbi.nlm.nih.gov/pubmed/32090487
http://dx.doi.org/10.15252/msb.20198870
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author Stanoev, Angel
Nandan, Akhilesh P
Koseska, Aneta
author_facet Stanoev, Angel
Nandan, Akhilesh P
Koseska, Aneta
author_sort Stanoev, Angel
collection PubMed
description How cells utilize surface receptors for chemoreception is a recurrent question spanning between physics and biology over the past few decades. However, the dynamical mechanism for processing time‐varying signals is still unclear. Using dynamical systems formalism to describe criticality in non‐equilibrium systems, we propose generic principle for temporal information processing through phase space trajectories using dynamic transient memory. In contrast to short‐term memory, dynamic memory generated via “ghost” attractor enables signal integration depending on stimulus history and thereby uniquely promotes integrating and interpreting complex temporal growth factor signals. We argue that this is a generic feature of receptor networks, the first layer of the cell that senses the changing environment. Using the experimentally established epidermal growth factor sensing system, we propose how recycling could provide self‐organized maintenance of the critical receptor concentration at the plasma membrane through a simple, fluctuation‐sensing mechanism. Processing of non‐stationary signals, a feature previously attributed only to neural networks, thus uniquely emerges for receptor networks organized at criticality.
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spelling pubmed-70367182020-03-02 Organization at criticality enables processing of time‐varying signals by receptor networks Stanoev, Angel Nandan, Akhilesh P Koseska, Aneta Mol Syst Biol Articles How cells utilize surface receptors for chemoreception is a recurrent question spanning between physics and biology over the past few decades. However, the dynamical mechanism for processing time‐varying signals is still unclear. Using dynamical systems formalism to describe criticality in non‐equilibrium systems, we propose generic principle for temporal information processing through phase space trajectories using dynamic transient memory. In contrast to short‐term memory, dynamic memory generated via “ghost” attractor enables signal integration depending on stimulus history and thereby uniquely promotes integrating and interpreting complex temporal growth factor signals. We argue that this is a generic feature of receptor networks, the first layer of the cell that senses the changing environment. Using the experimentally established epidermal growth factor sensing system, we propose how recycling could provide self‐organized maintenance of the critical receptor concentration at the plasma membrane through a simple, fluctuation‐sensing mechanism. Processing of non‐stationary signals, a feature previously attributed only to neural networks, thus uniquely emerges for receptor networks organized at criticality. John Wiley and Sons Inc. 2020-02-24 /pmc/articles/PMC7036718/ /pubmed/32090487 http://dx.doi.org/10.15252/msb.20198870 Text en © 2020 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Stanoev, Angel
Nandan, Akhilesh P
Koseska, Aneta
Organization at criticality enables processing of time‐varying signals by receptor networks
title Organization at criticality enables processing of time‐varying signals by receptor networks
title_full Organization at criticality enables processing of time‐varying signals by receptor networks
title_fullStr Organization at criticality enables processing of time‐varying signals by receptor networks
title_full_unstemmed Organization at criticality enables processing of time‐varying signals by receptor networks
title_short Organization at criticality enables processing of time‐varying signals by receptor networks
title_sort organization at criticality enables processing of time‐varying signals by receptor networks
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036718/
https://www.ncbi.nlm.nih.gov/pubmed/32090487
http://dx.doi.org/10.15252/msb.20198870
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