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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8472079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wuxin calmodulininteractionswithvoltagegatedsodiumchannels AT hongliang calmodulininteractionswithvoltagegatedsodiumchannels |