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Controlling the Synchronization of Molecular Oscillators through Indirect Coupling

In this article, we study the coupling of a collection of molecular oscillators, called repressilators, interacting indirectly through enzymatic saturation. We extended a measure of autocorrelation to identify the period of the whole system and to detect coupling behaviors. We explored the parameter...

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Detalles Bibliográficos
Autores principales: Inagaki, Shiho, Aubert-Kato, Nathanael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8877793/
https://www.ncbi.nlm.nih.gov/pubmed/35208369
http://dx.doi.org/10.3390/mi13020245
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author Inagaki, Shiho
Aubert-Kato, Nathanael
author_facet Inagaki, Shiho
Aubert-Kato, Nathanael
author_sort Inagaki, Shiho
collection PubMed
description In this article, we study the coupling of a collection of molecular oscillators, called repressilators, interacting indirectly through enzymatic saturation. We extended a measure of autocorrelation to identify the period of the whole system and to detect coupling behaviors. We explored the parameter space of concentrations of molecular species in each oscillator versus enzymatic saturation, and observed regions of uncoupled, partially, or fully coupled systems. In particular, we found a region that provided a sharp transition between no coupling, two coupled oscillators, and full coupling. In practical applications, signals from the environment can directly affect parameters such as local enzymatic saturation, and thus switch the system from a coupled to an uncoupled regime and vice-versa. Our parameter exploration can be used to guide the design of complex molecular systems, such as active materials or molecular robot controllers.
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spelling pubmed-88777932022-02-26 Controlling the Synchronization of Molecular Oscillators through Indirect Coupling Inagaki, Shiho Aubert-Kato, Nathanael Micromachines (Basel) Brief Report In this article, we study the coupling of a collection of molecular oscillators, called repressilators, interacting indirectly through enzymatic saturation. We extended a measure of autocorrelation to identify the period of the whole system and to detect coupling behaviors. We explored the parameter space of concentrations of molecular species in each oscillator versus enzymatic saturation, and observed regions of uncoupled, partially, or fully coupled systems. In particular, we found a region that provided a sharp transition between no coupling, two coupled oscillators, and full coupling. In practical applications, signals from the environment can directly affect parameters such as local enzymatic saturation, and thus switch the system from a coupled to an uncoupled regime and vice-versa. Our parameter exploration can be used to guide the design of complex molecular systems, such as active materials or molecular robot controllers. MDPI 2022-02-01 /pmc/articles/PMC8877793/ /pubmed/35208369 http://dx.doi.org/10.3390/mi13020245 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Inagaki, Shiho
Aubert-Kato, Nathanael
Controlling the Synchronization of Molecular Oscillators through Indirect Coupling
title Controlling the Synchronization of Molecular Oscillators through Indirect Coupling
title_full Controlling the Synchronization of Molecular Oscillators through Indirect Coupling
title_fullStr Controlling the Synchronization of Molecular Oscillators through Indirect Coupling
title_full_unstemmed Controlling the Synchronization of Molecular Oscillators through Indirect Coupling
title_short Controlling the Synchronization of Molecular Oscillators through Indirect Coupling
title_sort controlling the synchronization of molecular oscillators through indirect coupling
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8877793/
https://www.ncbi.nlm.nih.gov/pubmed/35208369
http://dx.doi.org/10.3390/mi13020245
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