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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...

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Detalles Bibliográficos
Autores principales: Hsu, Allen L., Ben-Johny, Manu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2023
Materias:
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.
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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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