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Ion channel chameleons: Switching ion selectivity by alternative splicing
Voltage-gated sodium and calcium channels are distinct, evolutionarily related ion channels that achieve remarkable ion selectivity despite sharing an overall similar structure. Classical studies have shown that ion selectivity is determined by specific binding of ions to the channel pore, enabled b...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017353/ https://www.ncbi.nlm.nih.gov/pubmed/36707054 http://dx.doi.org/10.1016/j.jbc.2023.102946 |
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author | Hsu, Allen L. Ben-Johny, Manu |
author_facet | Hsu, Allen L. Ben-Johny, Manu |
author_sort | Hsu, Allen L. |
collection | PubMed |
description | Voltage-gated sodium and calcium channels are distinct, evolutionarily related ion channels that achieve remarkable ion selectivity despite sharing an overall similar structure. Classical studies have shown that ion selectivity is determined by specific binding of ions to the channel pore, enabled by signature amino acid sequences within the selectivity filter (SF). By studying ancestral channels in the pond snail (Lymnaea stagnalis), Guan et al. showed in a recent JBC article that this well-established mechanism can be tuned by alternative splicing, allowing a single Ca(V)3 gene to encode both a Ca(2+)-permeable and an Na(+)-permeable channel depending on the cellular context. These findings shed light on mechanisms that tune ion selectivity in physiology and on the evolutionary basis of ion selectivity. |
format | Online Article Text |
id | pubmed-10017353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-100173532023-03-17 Ion channel chameleons: Switching ion selectivity by alternative splicing Hsu, Allen L. Ben-Johny, Manu J Biol Chem Editors' Pick Highlight Voltage-gated sodium and calcium channels are distinct, evolutionarily related ion channels that achieve remarkable ion selectivity despite sharing an overall similar structure. Classical studies have shown that ion selectivity is determined by specific binding of ions to the channel pore, enabled by signature amino acid sequences within the selectivity filter (SF). By studying ancestral channels in the pond snail (Lymnaea stagnalis), Guan et al. showed in a recent JBC article that this well-established mechanism can be tuned by alternative splicing, allowing a single Ca(V)3 gene to encode both a Ca(2+)-permeable and an Na(+)-permeable channel depending on the cellular context. These findings shed light on mechanisms that tune ion selectivity in physiology and on the evolutionary basis of ion selectivity. American Society for Biochemistry and Molecular Biology 2023-01-24 /pmc/articles/PMC10017353/ /pubmed/36707054 http://dx.doi.org/10.1016/j.jbc.2023.102946 Text en © 2023 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 Hsu, Allen L. Ben-Johny, Manu Ion channel chameleons: Switching ion selectivity by alternative splicing |
title | Ion channel chameleons: Switching ion selectivity by alternative splicing |
title_full | Ion channel chameleons: Switching ion selectivity by alternative splicing |
title_fullStr | Ion channel chameleons: Switching ion selectivity by alternative splicing |
title_full_unstemmed | Ion channel chameleons: Switching ion selectivity by alternative splicing |
title_short | Ion channel chameleons: Switching ion selectivity by alternative splicing |
title_sort | ion channel chameleons: switching ion selectivity by alternative splicing |
topic | Editors' Pick Highlight |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017353/ https://www.ncbi.nlm.nih.gov/pubmed/36707054 http://dx.doi.org/10.1016/j.jbc.2023.102946 |
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