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Membrane association and remodeling by intraflagellar transport protein IFT172
The cilium is an organelle used for motility and cellular signaling. Intraflagellar transport (IFT) is a process to move ciliary building blocks and signaling components into the cilium. How IFT controls the movement of ciliary components is currently poorly understood. IFT172 is the largest IFT sub...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224603/ https://www.ncbi.nlm.nih.gov/pubmed/30409972 http://dx.doi.org/10.1038/s41467-018-07037-9 |
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author | Wang, Qianmin Taschner, Michael Ganzinger, Kristina A. Kelley, Charlotte Villasenor, Alethia Heymann, Michael Schwille, Petra Lorentzen, Esben Mizuno, Naoko |
author_facet | Wang, Qianmin Taschner, Michael Ganzinger, Kristina A. Kelley, Charlotte Villasenor, Alethia Heymann, Michael Schwille, Petra Lorentzen, Esben Mizuno, Naoko |
author_sort | Wang, Qianmin |
collection | PubMed |
description | The cilium is an organelle used for motility and cellular signaling. Intraflagellar transport (IFT) is a process to move ciliary building blocks and signaling components into the cilium. How IFT controls the movement of ciliary components is currently poorly understood. IFT172 is the largest IFT subunit essential for ciliogenesis. Due to its large size, the characterization of IFT172 has been challenging. Using giant unilamellar vesicles (GUVs), we show that IFT172 is a membrane-interacting protein with the ability to remodel large membranes into small vesicles. Purified IFT172 has an architecture of two globular domains with a long rod-like protrusion, resembling the domain organization of coatomer proteins such as COPI-II or clathrin. IFT172 adopts two different conformations that can be manipulated by lipids or detergents: 1) an extended elongated conformation and 2) a globular closed architecture. Interestingly, the association of IFT172 with membranes is mutually exclusive with IFT57, implicating multiple functions for IFT172 within IFT. |
format | Online Article Text |
id | pubmed-6224603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62246032018-11-13 Membrane association and remodeling by intraflagellar transport protein IFT172 Wang, Qianmin Taschner, Michael Ganzinger, Kristina A. Kelley, Charlotte Villasenor, Alethia Heymann, Michael Schwille, Petra Lorentzen, Esben Mizuno, Naoko Nat Commun Article The cilium is an organelle used for motility and cellular signaling. Intraflagellar transport (IFT) is a process to move ciliary building blocks and signaling components into the cilium. How IFT controls the movement of ciliary components is currently poorly understood. IFT172 is the largest IFT subunit essential for ciliogenesis. Due to its large size, the characterization of IFT172 has been challenging. Using giant unilamellar vesicles (GUVs), we show that IFT172 is a membrane-interacting protein with the ability to remodel large membranes into small vesicles. Purified IFT172 has an architecture of two globular domains with a long rod-like protrusion, resembling the domain organization of coatomer proteins such as COPI-II or clathrin. IFT172 adopts two different conformations that can be manipulated by lipids or detergents: 1) an extended elongated conformation and 2) a globular closed architecture. Interestingly, the association of IFT172 with membranes is mutually exclusive with IFT57, implicating multiple functions for IFT172 within IFT. Nature Publishing Group UK 2018-11-08 /pmc/articles/PMC6224603/ /pubmed/30409972 http://dx.doi.org/10.1038/s41467-018-07037-9 Text en © The Author(s) 2018 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 Wang, Qianmin Taschner, Michael Ganzinger, Kristina A. Kelley, Charlotte Villasenor, Alethia Heymann, Michael Schwille, Petra Lorentzen, Esben Mizuno, Naoko Membrane association and remodeling by intraflagellar transport protein IFT172 |
title | Membrane association and remodeling by intraflagellar transport protein IFT172 |
title_full | Membrane association and remodeling by intraflagellar transport protein IFT172 |
title_fullStr | Membrane association and remodeling by intraflagellar transport protein IFT172 |
title_full_unstemmed | Membrane association and remodeling by intraflagellar transport protein IFT172 |
title_short | Membrane association and remodeling by intraflagellar transport protein IFT172 |
title_sort | membrane association and remodeling by intraflagellar transport protein ift172 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224603/ https://www.ncbi.nlm.nih.gov/pubmed/30409972 http://dx.doi.org/10.1038/s41467-018-07037-9 |
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