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Mechanically-primed voltage-gated proton channels from angiosperm plants
Voltage-gated and mechanically-gated ion channels are distinct classes of membrane proteins that conduct ions across gated pores and are turned on by electrical or mechanical stimuli, respectively. Here, we describe an Hv channel (a.k.a voltage-dependent H(+) channel) from the angiosperm plant A. th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657467/ https://www.ncbi.nlm.nih.gov/pubmed/37980353 http://dx.doi.org/10.1038/s41467-023-43280-5 |
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author | Zhao, Chang Webster, Parker D. De Angeli, Alexis Tombola, Francesco |
author_facet | Zhao, Chang Webster, Parker D. De Angeli, Alexis Tombola, Francesco |
author_sort | Zhao, Chang |
collection | PubMed |
description | Voltage-gated and mechanically-gated ion channels are distinct classes of membrane proteins that conduct ions across gated pores and are turned on by electrical or mechanical stimuli, respectively. Here, we describe an Hv channel (a.k.a voltage-dependent H(+) channel) from the angiosperm plant A. thaliana that gates with a unique modality as it is turned on by an electrical stimulus only after exposure to a mechanical stimulus, a process that we call priming. The channel localizes in the vascular tissue and has homologs in vascular plants. We find that mechanical priming is not required for activation of non-angiosperm Hvs. Guided by AI-generated structural models of plant Hv homologs, we identify a set of residues playing a crucial role in mechanical priming. We propose that Hvs from angiosperm plants require priming because of a network of hydrophilic/charged residues that locks the channels in a silent resting conformation. Mechanical stimuli destabilize the network allowing the conduction pathway to turn on. In contrast to many other channels and receptors, Hv proteins are not thought to possess mechanisms such as inactivation or desensitization. Our findings demonstrate that angiosperm Hv channels are electrically silent until a mechanical stimulation turns on their voltage-dependent activity. |
format | Online Article Text |
id | pubmed-10657467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106574672023-11-18 Mechanically-primed voltage-gated proton channels from angiosperm plants Zhao, Chang Webster, Parker D. De Angeli, Alexis Tombola, Francesco Nat Commun Article Voltage-gated and mechanically-gated ion channels are distinct classes of membrane proteins that conduct ions across gated pores and are turned on by electrical or mechanical stimuli, respectively. Here, we describe an Hv channel (a.k.a voltage-dependent H(+) channel) from the angiosperm plant A. thaliana that gates with a unique modality as it is turned on by an electrical stimulus only after exposure to a mechanical stimulus, a process that we call priming. The channel localizes in the vascular tissue and has homologs in vascular plants. We find that mechanical priming is not required for activation of non-angiosperm Hvs. Guided by AI-generated structural models of plant Hv homologs, we identify a set of residues playing a crucial role in mechanical priming. We propose that Hvs from angiosperm plants require priming because of a network of hydrophilic/charged residues that locks the channels in a silent resting conformation. Mechanical stimuli destabilize the network allowing the conduction pathway to turn on. In contrast to many other channels and receptors, Hv proteins are not thought to possess mechanisms such as inactivation or desensitization. Our findings demonstrate that angiosperm Hv channels are electrically silent until a mechanical stimulation turns on their voltage-dependent activity. Nature Publishing Group UK 2023-11-18 /pmc/articles/PMC10657467/ /pubmed/37980353 http://dx.doi.org/10.1038/s41467-023-43280-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhao, Chang Webster, Parker D. De Angeli, Alexis Tombola, Francesco Mechanically-primed voltage-gated proton channels from angiosperm plants |
title | Mechanically-primed voltage-gated proton channels from angiosperm plants |
title_full | Mechanically-primed voltage-gated proton channels from angiosperm plants |
title_fullStr | Mechanically-primed voltage-gated proton channels from angiosperm plants |
title_full_unstemmed | Mechanically-primed voltage-gated proton channels from angiosperm plants |
title_short | Mechanically-primed voltage-gated proton channels from angiosperm plants |
title_sort | mechanically-primed voltage-gated proton channels from angiosperm plants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657467/ https://www.ncbi.nlm.nih.gov/pubmed/37980353 http://dx.doi.org/10.1038/s41467-023-43280-5 |
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