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TbIRK is a signature sequence free potassium channel from Trypanosoma brucei locating to acidocalcisomes
Potassium channels from prokaryotes and eukaryotes are usually recognized by a typical amino acid sequence TXTGY(F)G representing the ionic selectivity filter. Using a screening approach with ion channel family profiles but without the above motif, we identified a gene in Trypanosoma brucei that exh...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429665/ https://www.ncbi.nlm.nih.gov/pubmed/28386071 http://dx.doi.org/10.1038/s41598-017-00752-1 |
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author | Steinmann, Michael E. Schmidt, Remo S. Bütikofer, Peter Mäser, Pascal Sigel, Erwin |
author_facet | Steinmann, Michael E. Schmidt, Remo S. Bütikofer, Peter Mäser, Pascal Sigel, Erwin |
author_sort | Steinmann, Michael E. |
collection | PubMed |
description | Potassium channels from prokaryotes and eukaryotes are usually recognized by a typical amino acid sequence TXTGY(F)G representing the ionic selectivity filter. Using a screening approach with ion channel family profiles but without the above motif, we identified a gene in Trypanosoma brucei that exhibits homology to inward rectifying potassium channels. We report here cloning of this ion channel named TbIRK. The protein is localized to acidocalcisomes in procyclic and in bloodstream form parasites. Functional properties of this channel were established after expression in Xenopus oocytes. Currents recorded in potassium medium show inward rectification and little time dependence. Surprisingly, this channel retains selectivity for potassium ions over sodium ions >7, in spite of the lack of the classical selectivity filter. The sequence GGYVG was predicted in silico to replace this filter motif. Point mutations of the corresponding glycine residues confirmed this at the functional level. The channel is inhibited by caesium ions but remains unaffected by barium ions up to 10 mM. TbIRK is to our knowledge the first potassium channel in T. brucei that localizes to the acidocalcisomes, organelles involved in the storage of phosphates and the response to osmotic stress that occurs during the life cycle of trypanosomes. |
format | Online Article Text |
id | pubmed-5429665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54296652017-05-15 TbIRK is a signature sequence free potassium channel from Trypanosoma brucei locating to acidocalcisomes Steinmann, Michael E. Schmidt, Remo S. Bütikofer, Peter Mäser, Pascal Sigel, Erwin Sci Rep Article Potassium channels from prokaryotes and eukaryotes are usually recognized by a typical amino acid sequence TXTGY(F)G representing the ionic selectivity filter. Using a screening approach with ion channel family profiles but without the above motif, we identified a gene in Trypanosoma brucei that exhibits homology to inward rectifying potassium channels. We report here cloning of this ion channel named TbIRK. The protein is localized to acidocalcisomes in procyclic and in bloodstream form parasites. Functional properties of this channel were established after expression in Xenopus oocytes. Currents recorded in potassium medium show inward rectification and little time dependence. Surprisingly, this channel retains selectivity for potassium ions over sodium ions >7, in spite of the lack of the classical selectivity filter. The sequence GGYVG was predicted in silico to replace this filter motif. Point mutations of the corresponding glycine residues confirmed this at the functional level. The channel is inhibited by caesium ions but remains unaffected by barium ions up to 10 mM. TbIRK is to our knowledge the first potassium channel in T. brucei that localizes to the acidocalcisomes, organelles involved in the storage of phosphates and the response to osmotic stress that occurs during the life cycle of trypanosomes. Nature Publishing Group UK 2017-04-06 /pmc/articles/PMC5429665/ /pubmed/28386071 http://dx.doi.org/10.1038/s41598-017-00752-1 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Steinmann, Michael E. Schmidt, Remo S. Bütikofer, Peter Mäser, Pascal Sigel, Erwin TbIRK is a signature sequence free potassium channel from Trypanosoma brucei locating to acidocalcisomes |
title | TbIRK is a signature sequence free potassium channel from Trypanosoma brucei locating to acidocalcisomes |
title_full | TbIRK is a signature sequence free potassium channel from Trypanosoma brucei locating to acidocalcisomes |
title_fullStr | TbIRK is a signature sequence free potassium channel from Trypanosoma brucei locating to acidocalcisomes |
title_full_unstemmed | TbIRK is a signature sequence free potassium channel from Trypanosoma brucei locating to acidocalcisomes |
title_short | TbIRK is a signature sequence free potassium channel from Trypanosoma brucei locating to acidocalcisomes |
title_sort | tbirk is a signature sequence free potassium channel from trypanosoma brucei locating to acidocalcisomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429665/ https://www.ncbi.nlm.nih.gov/pubmed/28386071 http://dx.doi.org/10.1038/s41598-017-00752-1 |
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