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Information theoretical quantification of cooperativity in signalling complexes

BACKGROUND: Intra-cellular information exchange, propelled by cascades of interacting signalling proteins, is essential for the proper functioning and survival of cells. Now that the interactome of several organisms is being mapped and several structural mechanisms of cooperativity at the molecular...

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Autores principales: Lenaerts, Tom, Ferkinghoff-Borg, Jesper, Schymkowitz, Joost, Rousseau, Frederic
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637831/
https://www.ncbi.nlm.nih.gov/pubmed/19149897
http://dx.doi.org/10.1186/1752-0509-3-9
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author Lenaerts, Tom
Ferkinghoff-Borg, Jesper
Schymkowitz, Joost
Rousseau, Frederic
author_facet Lenaerts, Tom
Ferkinghoff-Borg, Jesper
Schymkowitz, Joost
Rousseau, Frederic
author_sort Lenaerts, Tom
collection PubMed
description BACKGROUND: Intra-cellular information exchange, propelled by cascades of interacting signalling proteins, is essential for the proper functioning and survival of cells. Now that the interactome of several organisms is being mapped and several structural mechanisms of cooperativity at the molecular level in proteins have been elucidated, the formalization of this fundamental quantity, i.e. information, in these very diverse biological contexts becomes feasible. RESULTS: We show here that Shannon's mutual information quantifies information in biological system and more specifically the cooperativity inherent to the assembly of macromolecular complexes. We show how protein complexes can be considered as particular instances of noisy communication channels. Further we show, using a portion of the p27 regulatory pathway, how classical equilibrium thermodynamic quantities such as binding affinities and chemical potentials can be used to quantify information exchange but also to determine engineering properties such as channel noise and channel capacity. As such, this information measure identifies and quantifies those protein concentrations that render the biochemical system most effective in switching between the active and inactive state of the intracellular process. CONCLUSION: The proposed framework provides a new and original approach to analyse the effects of cooperativity in the assembly of macromolecular complexes. It shows the conditions, provided by the protein concentrations, for which a particular system acts most effectively, i.e. exchanges the most information. As such this framework opens the possibility of grasping biological qualities such as system sensitivity, robustness or plasticity directly in terms of their effect on information exchange. Although these parameters might also be derived using classical thermodynamic parameters, a recasting of biological signalling in terms of information exchange offers an alternative framework for visualising network cooperativity that might in some cases be more intuitive.
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spelling pubmed-26378312009-02-10 Information theoretical quantification of cooperativity in signalling complexes Lenaerts, Tom Ferkinghoff-Borg, Jesper Schymkowitz, Joost Rousseau, Frederic BMC Syst Biol Research Article BACKGROUND: Intra-cellular information exchange, propelled by cascades of interacting signalling proteins, is essential for the proper functioning and survival of cells. Now that the interactome of several organisms is being mapped and several structural mechanisms of cooperativity at the molecular level in proteins have been elucidated, the formalization of this fundamental quantity, i.e. information, in these very diverse biological contexts becomes feasible. RESULTS: We show here that Shannon's mutual information quantifies information in biological system and more specifically the cooperativity inherent to the assembly of macromolecular complexes. We show how protein complexes can be considered as particular instances of noisy communication channels. Further we show, using a portion of the p27 regulatory pathway, how classical equilibrium thermodynamic quantities such as binding affinities and chemical potentials can be used to quantify information exchange but also to determine engineering properties such as channel noise and channel capacity. As such, this information measure identifies and quantifies those protein concentrations that render the biochemical system most effective in switching between the active and inactive state of the intracellular process. CONCLUSION: The proposed framework provides a new and original approach to analyse the effects of cooperativity in the assembly of macromolecular complexes. It shows the conditions, provided by the protein concentrations, for which a particular system acts most effectively, i.e. exchanges the most information. As such this framework opens the possibility of grasping biological qualities such as system sensitivity, robustness or plasticity directly in terms of their effect on information exchange. Although these parameters might also be derived using classical thermodynamic parameters, a recasting of biological signalling in terms of information exchange offers an alternative framework for visualising network cooperativity that might in some cases be more intuitive. BioMed Central 2009-01-16 /pmc/articles/PMC2637831/ /pubmed/19149897 http://dx.doi.org/10.1186/1752-0509-3-9 Text en Copyright © 2009 Lenaerts et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lenaerts, Tom
Ferkinghoff-Borg, Jesper
Schymkowitz, Joost
Rousseau, Frederic
Information theoretical quantification of cooperativity in signalling complexes
title Information theoretical quantification of cooperativity in signalling complexes
title_full Information theoretical quantification of cooperativity in signalling complexes
title_fullStr Information theoretical quantification of cooperativity in signalling complexes
title_full_unstemmed Information theoretical quantification of cooperativity in signalling complexes
title_short Information theoretical quantification of cooperativity in signalling complexes
title_sort information theoretical quantification of cooperativity in signalling complexes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637831/
https://www.ncbi.nlm.nih.gov/pubmed/19149897
http://dx.doi.org/10.1186/1752-0509-3-9
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