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Na(v)igating the intricacies of cellular machinery
Voltage-gated sodium channels (Na(V)s) underlie the initiation of action potentials in various excitable cell types and are regulated by channel-interacting proteins, including the cellular calcium sensor calmodulin and fibroblast growth factor homologous factors. Both of these are known to bind the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8214083/ https://www.ncbi.nlm.nih.gov/pubmed/34048713 http://dx.doi.org/10.1016/j.jbc.2021.100832 |
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author | Nathan, Sara Gabelli, Sandra B. |
author_facet | Nathan, Sara Gabelli, Sandra B. |
author_sort | Nathan, Sara |
collection | PubMed |
description | Voltage-gated sodium channels (Na(V)s) underlie the initiation of action potentials in various excitable cell types and are regulated by channel-interacting proteins, including the cellular calcium sensor calmodulin and fibroblast growth factor homologous factors. Both of these are known to bind the Na(V) cytosolic C-terminal domain and modulate the channel’s electrophysiology, but it was unknown whether they had any allosteric interactions with each other. A recent rigorous study provides insights into the molecular interactions of these ion channels and their partners that crucially take the cellular landscape into consideration. |
format | Online Article Text |
id | pubmed-8214083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-82140832021-06-21 Na(v)igating the intricacies of cellular machinery Nathan, Sara Gabelli, Sandra B. J Biol Chem Editors' Pick Highlight Voltage-gated sodium channels (Na(V)s) underlie the initiation of action potentials in various excitable cell types and are regulated by channel-interacting proteins, including the cellular calcium sensor calmodulin and fibroblast growth factor homologous factors. Both of these are known to bind the Na(V) cytosolic C-terminal domain and modulate the channel’s electrophysiology, but it was unknown whether they had any allosteric interactions with each other. A recent rigorous study provides insights into the molecular interactions of these ion channels and their partners that crucially take the cellular landscape into consideration. American Society for Biochemistry and Molecular Biology 2021-05-26 /pmc/articles/PMC8214083/ /pubmed/34048713 http://dx.doi.org/10.1016/j.jbc.2021.100832 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Editors' Pick Highlight Nathan, Sara Gabelli, Sandra B. Na(v)igating the intricacies of cellular machinery |
title | Na(v)igating the intricacies of cellular machinery |
title_full | Na(v)igating the intricacies of cellular machinery |
title_fullStr | Na(v)igating the intricacies of cellular machinery |
title_full_unstemmed | Na(v)igating the intricacies of cellular machinery |
title_short | Na(v)igating the intricacies of cellular machinery |
title_sort | na(v)igating the intricacies of cellular machinery |
topic | Editors' Pick Highlight |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8214083/ https://www.ncbi.nlm.nih.gov/pubmed/34048713 http://dx.doi.org/10.1016/j.jbc.2021.100832 |
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