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Partners in Crime: Towards New Ways of Targeting Calcium Channels

The characterization of calcium channel interactome in the last decades opened a new way of perceiving ion channel function and regulation. Partner proteins of ion channels can now be considered as major components of the calcium homeostatic mechanisms, while the reinforcement or disruption of their...

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Detalles Bibliográficos
Autores principales: Noyer, Lucile, Lemonnier, Loic, Mariot, Pascal, Gkika, Dimitra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940757/
https://www.ncbi.nlm.nih.gov/pubmed/31888223
http://dx.doi.org/10.3390/ijms20246344
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author Noyer, Lucile
Lemonnier, Loic
Mariot, Pascal
Gkika, Dimitra
author_facet Noyer, Lucile
Lemonnier, Loic
Mariot, Pascal
Gkika, Dimitra
author_sort Noyer, Lucile
collection PubMed
description The characterization of calcium channel interactome in the last decades opened a new way of perceiving ion channel function and regulation. Partner proteins of ion channels can now be considered as major components of the calcium homeostatic mechanisms, while the reinforcement or disruption of their interaction with the channel units now represents an attractive target in research and therapeutics. In this review we will focus on the targeting of calcium channel partner proteins in order to act on the channel activity, and on its consequences for cell and organism physiology. Given the recent advances in the partner proteins’ identification, characterization, as well as in the resolution of their interaction domain structures, we will develop the latest findings on the interacting proteins of the following channels: voltage-dependent calcium channels, transient receptor potential and ORAI channels, and inositol 1,4,5-trisphosphate receptor.
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spelling pubmed-69407572020-01-09 Partners in Crime: Towards New Ways of Targeting Calcium Channels Noyer, Lucile Lemonnier, Loic Mariot, Pascal Gkika, Dimitra Int J Mol Sci Review The characterization of calcium channel interactome in the last decades opened a new way of perceiving ion channel function and regulation. Partner proteins of ion channels can now be considered as major components of the calcium homeostatic mechanisms, while the reinforcement or disruption of their interaction with the channel units now represents an attractive target in research and therapeutics. In this review we will focus on the targeting of calcium channel partner proteins in order to act on the channel activity, and on its consequences for cell and organism physiology. Given the recent advances in the partner proteins’ identification, characterization, as well as in the resolution of their interaction domain structures, we will develop the latest findings on the interacting proteins of the following channels: voltage-dependent calcium channels, transient receptor potential and ORAI channels, and inositol 1,4,5-trisphosphate receptor. MDPI 2019-12-16 /pmc/articles/PMC6940757/ /pubmed/31888223 http://dx.doi.org/10.3390/ijms20246344 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Noyer, Lucile
Lemonnier, Loic
Mariot, Pascal
Gkika, Dimitra
Partners in Crime: Towards New Ways of Targeting Calcium Channels
title Partners in Crime: Towards New Ways of Targeting Calcium Channels
title_full Partners in Crime: Towards New Ways of Targeting Calcium Channels
title_fullStr Partners in Crime: Towards New Ways of Targeting Calcium Channels
title_full_unstemmed Partners in Crime: Towards New Ways of Targeting Calcium Channels
title_short Partners in Crime: Towards New Ways of Targeting Calcium Channels
title_sort partners in crime: towards new ways of targeting calcium channels
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940757/
https://www.ncbi.nlm.nih.gov/pubmed/31888223
http://dx.doi.org/10.3390/ijms20246344
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