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Two flagellar BAR domain proteins in Trypanosoma brucei with stage-specific regulation
Trypanosomes are masters of adaptation to different host environments during their complex life cycle. Large-scale proteomic approaches provide information on changes at the cellular level, and in a systematic way. However, detailed work on single components is necessary to understand the adaptation...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078803/ https://www.ncbi.nlm.nih.gov/pubmed/27779220 http://dx.doi.org/10.1038/srep35826 |
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author | Cicova, Zdenka Dejung, Mario Skalicky, Tomas Eisenhuth, Nicole Hanselmann, Steffen Morriswood, Brooke Figueiredo, Luisa M. Butter, Falk Janzen, Christian J. |
author_facet | Cicova, Zdenka Dejung, Mario Skalicky, Tomas Eisenhuth, Nicole Hanselmann, Steffen Morriswood, Brooke Figueiredo, Luisa M. Butter, Falk Janzen, Christian J. |
author_sort | Cicova, Zdenka |
collection | PubMed |
description | Trypanosomes are masters of adaptation to different host environments during their complex life cycle. Large-scale proteomic approaches provide information on changes at the cellular level, and in a systematic way. However, detailed work on single components is necessary to understand the adaptation mechanisms on a molecular level. Here, we have performed a detailed characterization of a bloodstream form (BSF) stage-specific putative flagellar host adaptation factor Tb927.11.2400, identified previously in a SILAC-based comparative proteome study. Tb927.11.2400 shares 38% amino acid identity with TbFlabarin (Tb927.11.2410), a procyclic form (PCF) stage-specific flagellar BAR domain protein. We named Tb927.11.2400 TbFlabarin-like (TbFlabarinL), and demonstrate that it originates from a gene duplication event, which occurred in the African trypanosomes. TbFlabarinL is not essential for the growth of the parasites under cell culture conditions and it is dispensable for developmental differentiation from BSF to the PCF in vitro. We generated TbFlabarinL-specific antibodies, and showed that it localizes in the flagellum. Co-immunoprecipitation experiments together with a biochemical cell fractionation suggest a dual association of TbFlabarinL with the flagellar membrane and the components of the paraflagellar rod. |
format | Online Article Text |
id | pubmed-5078803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50788032016-10-31 Two flagellar BAR domain proteins in Trypanosoma brucei with stage-specific regulation Cicova, Zdenka Dejung, Mario Skalicky, Tomas Eisenhuth, Nicole Hanselmann, Steffen Morriswood, Brooke Figueiredo, Luisa M. Butter, Falk Janzen, Christian J. Sci Rep Article Trypanosomes are masters of adaptation to different host environments during their complex life cycle. Large-scale proteomic approaches provide information on changes at the cellular level, and in a systematic way. However, detailed work on single components is necessary to understand the adaptation mechanisms on a molecular level. Here, we have performed a detailed characterization of a bloodstream form (BSF) stage-specific putative flagellar host adaptation factor Tb927.11.2400, identified previously in a SILAC-based comparative proteome study. Tb927.11.2400 shares 38% amino acid identity with TbFlabarin (Tb927.11.2410), a procyclic form (PCF) stage-specific flagellar BAR domain protein. We named Tb927.11.2400 TbFlabarin-like (TbFlabarinL), and demonstrate that it originates from a gene duplication event, which occurred in the African trypanosomes. TbFlabarinL is not essential for the growth of the parasites under cell culture conditions and it is dispensable for developmental differentiation from BSF to the PCF in vitro. We generated TbFlabarinL-specific antibodies, and showed that it localizes in the flagellum. Co-immunoprecipitation experiments together with a biochemical cell fractionation suggest a dual association of TbFlabarinL with the flagellar membrane and the components of the paraflagellar rod. Nature Publishing Group 2016-10-25 /pmc/articles/PMC5078803/ /pubmed/27779220 http://dx.doi.org/10.1038/srep35826 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Cicova, Zdenka Dejung, Mario Skalicky, Tomas Eisenhuth, Nicole Hanselmann, Steffen Morriswood, Brooke Figueiredo, Luisa M. Butter, Falk Janzen, Christian J. Two flagellar BAR domain proteins in Trypanosoma brucei with stage-specific regulation |
title | Two flagellar BAR domain proteins in Trypanosoma brucei with stage-specific regulation |
title_full | Two flagellar BAR domain proteins in Trypanosoma brucei with stage-specific regulation |
title_fullStr | Two flagellar BAR domain proteins in Trypanosoma brucei with stage-specific regulation |
title_full_unstemmed | Two flagellar BAR domain proteins in Trypanosoma brucei with stage-specific regulation |
title_short | Two flagellar BAR domain proteins in Trypanosoma brucei with stage-specific regulation |
title_sort | two flagellar bar domain proteins in trypanosoma brucei with stage-specific regulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078803/ https://www.ncbi.nlm.nih.gov/pubmed/27779220 http://dx.doi.org/10.1038/srep35826 |
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