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Calmodulin Interactions with Voltage-Gated Sodium Channels

Calmodulin (CaM) is a small protein that acts as a ubiquitous signal transducer and regulates neuronal plasticity, muscle contraction, and immune response. It interacts with ion channels and plays regulatory roles in cellular electrophysiology. CaM modulates the voltage-gated sodium channel gating p...

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Detalles Bibliográficos
Autores principales: Wu, Xin, Hong, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472079/
https://www.ncbi.nlm.nih.gov/pubmed/34575961
http://dx.doi.org/10.3390/ijms22189798
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author Wu, Xin
Hong, Liang
author_facet Wu, Xin
Hong, Liang
author_sort Wu, Xin
collection PubMed
description Calmodulin (CaM) is a small protein that acts as a ubiquitous signal transducer and regulates neuronal plasticity, muscle contraction, and immune response. It interacts with ion channels and plays regulatory roles in cellular electrophysiology. CaM modulates the voltage-gated sodium channel gating process, alters sodium current density, and regulates sodium channel protein trafficking and expression. Many mutations in the CaM-binding IQ domain give rise to diseases including epilepsy, autism, and arrhythmias by interfering with CaM interaction with the channel. In the present review, we discuss CaM interactions with the voltage-gated sodium channel and modulators involved in CaM regulation, as well as summarize CaM-binding IQ domain mutations associated with human diseases in the voltage-gated sodium channel family.
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spelling pubmed-84720792021-09-28 Calmodulin Interactions with Voltage-Gated Sodium Channels Wu, Xin Hong, Liang Int J Mol Sci Review Calmodulin (CaM) is a small protein that acts as a ubiquitous signal transducer and regulates neuronal plasticity, muscle contraction, and immune response. It interacts with ion channels and plays regulatory roles in cellular electrophysiology. CaM modulates the voltage-gated sodium channel gating process, alters sodium current density, and regulates sodium channel protein trafficking and expression. Many mutations in the CaM-binding IQ domain give rise to diseases including epilepsy, autism, and arrhythmias by interfering with CaM interaction with the channel. In the present review, we discuss CaM interactions with the voltage-gated sodium channel and modulators involved in CaM regulation, as well as summarize CaM-binding IQ domain mutations associated with human diseases in the voltage-gated sodium channel family. MDPI 2021-09-10 /pmc/articles/PMC8472079/ /pubmed/34575961 http://dx.doi.org/10.3390/ijms22189798 Text en © 2021 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 Review
Wu, Xin
Hong, Liang
Calmodulin Interactions with Voltage-Gated Sodium Channels
title Calmodulin Interactions with Voltage-Gated Sodium Channels
title_full Calmodulin Interactions with Voltage-Gated Sodium Channels
title_fullStr Calmodulin Interactions with Voltage-Gated Sodium Channels
title_full_unstemmed Calmodulin Interactions with Voltage-Gated Sodium Channels
title_short Calmodulin Interactions with Voltage-Gated Sodium Channels
title_sort calmodulin interactions with voltage-gated sodium channels
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472079/
https://www.ncbi.nlm.nih.gov/pubmed/34575961
http://dx.doi.org/10.3390/ijms22189798
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