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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...

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Autores principales: Wang, Qianmin, Taschner, Michael, Ganzinger, Kristina A., Kelley, Charlotte, Villasenor, Alethia, Heymann, Michael, Schwille, Petra, Lorentzen, Esben, Mizuno, Naoko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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