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Vertebrate OTOP1 is also an alkali-activated channel
Although alkaline sensation is critical for survival, alkali-activated receptors are yet to be identified in vertebrates. Here, we showed that the OTOP1 channel can be directly activated by extracellular alkali. Notably, OTOP1 biphasically mediated proton influx and efflux with extracellular acid an...
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/PMC9810603/ https://www.ncbi.nlm.nih.gov/pubmed/36596786 http://dx.doi.org/10.1038/s41467-022-35754-9 |
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author | Tian, Lifeng Zhang, Hao Yang, Shilong Luo, Anna Kamau, Peter Muiruri Hu, Jingmei Luo, Lei Lai, Ren |
author_facet | Tian, Lifeng Zhang, Hao Yang, Shilong Luo, Anna Kamau, Peter Muiruri Hu, Jingmei Luo, Lei Lai, Ren |
author_sort | Tian, Lifeng |
collection | PubMed |
description | Although alkaline sensation is critical for survival, alkali-activated receptors are yet to be identified in vertebrates. Here, we showed that the OTOP1 channel can be directly activated by extracellular alkali. Notably, OTOP1 biphasically mediated proton influx and efflux with extracellular acid and base stimulation, respectively. Mutations of K221 and R554 at the S5–S6 and S11–S12 linkers significantly reduced alkali affinity without affecting acid activation, suggesting that different domains are responsible for acid- and alkali-activation of OTOP1. The selectivity for H(+) was significantly higher in OTOP1 activated by alkali than that by acid, further suggesting that the two activations might be independent gating processes. Given that the alkali-activation of OTOP1 and the required key residues were conserved in the six representative vertebrates, we cautiously propose that OTOP1 participates in alkaline sensation in vertebrates. Thus, our study identified OTOP1 as an alkali-activated channel. |
format | Online Article Text |
id | pubmed-9810603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98106032023-01-05 Vertebrate OTOP1 is also an alkali-activated channel Tian, Lifeng Zhang, Hao Yang, Shilong Luo, Anna Kamau, Peter Muiruri Hu, Jingmei Luo, Lei Lai, Ren Nat Commun Article Although alkaline sensation is critical for survival, alkali-activated receptors are yet to be identified in vertebrates. Here, we showed that the OTOP1 channel can be directly activated by extracellular alkali. Notably, OTOP1 biphasically mediated proton influx and efflux with extracellular acid and base stimulation, respectively. Mutations of K221 and R554 at the S5–S6 and S11–S12 linkers significantly reduced alkali affinity without affecting acid activation, suggesting that different domains are responsible for acid- and alkali-activation of OTOP1. The selectivity for H(+) was significantly higher in OTOP1 activated by alkali than that by acid, further suggesting that the two activations might be independent gating processes. Given that the alkali-activation of OTOP1 and the required key residues were conserved in the six representative vertebrates, we cautiously propose that OTOP1 participates in alkaline sensation in vertebrates. Thus, our study identified OTOP1 as an alkali-activated channel. Nature Publishing Group UK 2023-01-03 /pmc/articles/PMC9810603/ /pubmed/36596786 http://dx.doi.org/10.1038/s41467-022-35754-9 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Tian, Lifeng Zhang, Hao Yang, Shilong Luo, Anna Kamau, Peter Muiruri Hu, Jingmei Luo, Lei Lai, Ren Vertebrate OTOP1 is also an alkali-activated channel |
title | Vertebrate OTOP1 is also an alkali-activated channel |
title_full | Vertebrate OTOP1 is also an alkali-activated channel |
title_fullStr | Vertebrate OTOP1 is also an alkali-activated channel |
title_full_unstemmed | Vertebrate OTOP1 is also an alkali-activated channel |
title_short | Vertebrate OTOP1 is also an alkali-activated channel |
title_sort | vertebrate otop1 is also an alkali-activated channel |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810603/ https://www.ncbi.nlm.nih.gov/pubmed/36596786 http://dx.doi.org/10.1038/s41467-022-35754-9 |
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