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The molecular organization of differentially curved caveolae indicates bendable structural units at the plasma membrane

Caveolae are small coated plasma membrane invaginations with diverse functions. Caveolae undergo curvature changes. Yet, it is unclear which proteins regulate this process. To address this gap, we develop a correlative stimulated emission depletion (STED) fluorescence and platinum replica electron m...

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Autores principales: Matthaeus, Claudia, Sochacki, Kem A., Dickey, Andrea M., Puchkov, Dmytro, Haucke, Volker, Lehmann, Martin, Taraska, Justin W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700719/
https://www.ncbi.nlm.nih.gov/pubmed/36433988
http://dx.doi.org/10.1038/s41467-022-34958-3
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author Matthaeus, Claudia
Sochacki, Kem A.
Dickey, Andrea M.
Puchkov, Dmytro
Haucke, Volker
Lehmann, Martin
Taraska, Justin W.
author_facet Matthaeus, Claudia
Sochacki, Kem A.
Dickey, Andrea M.
Puchkov, Dmytro
Haucke, Volker
Lehmann, Martin
Taraska, Justin W.
author_sort Matthaeus, Claudia
collection PubMed
description Caveolae are small coated plasma membrane invaginations with diverse functions. Caveolae undergo curvature changes. Yet, it is unclear which proteins regulate this process. To address this gap, we develop a correlative stimulated emission depletion (STED) fluorescence and platinum replica electron microscopy imaging (CLEM) method to image proteins at single caveolae. Caveolins and cavins are found at all caveolae, independent of curvature. EHD2 is detected at both low and highly curved caveolae. Pacsin2 associates with low curved caveolae and EHBP1 with mostly highly curved caveolae. Dynamin is absent from caveolae. Cells lacking dynamin show no substantial changes to caveolae, suggesting that dynamin is not directly involved in caveolae curvature. We propose a model where caveolins, cavins, and EHD2 assemble as a cohesive structural unit regulated by intermittent associations with pacsin2 and EHBP1. These coats can flatten and curve to enable lipid traffic, signaling, and changes to the surface area of the cell.
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spelling pubmed-97007192022-11-27 The molecular organization of differentially curved caveolae indicates bendable structural units at the plasma membrane Matthaeus, Claudia Sochacki, Kem A. Dickey, Andrea M. Puchkov, Dmytro Haucke, Volker Lehmann, Martin Taraska, Justin W. Nat Commun Article Caveolae are small coated plasma membrane invaginations with diverse functions. Caveolae undergo curvature changes. Yet, it is unclear which proteins regulate this process. To address this gap, we develop a correlative stimulated emission depletion (STED) fluorescence and platinum replica electron microscopy imaging (CLEM) method to image proteins at single caveolae. Caveolins and cavins are found at all caveolae, independent of curvature. EHD2 is detected at both low and highly curved caveolae. Pacsin2 associates with low curved caveolae and EHBP1 with mostly highly curved caveolae. Dynamin is absent from caveolae. Cells lacking dynamin show no substantial changes to caveolae, suggesting that dynamin is not directly involved in caveolae curvature. We propose a model where caveolins, cavins, and EHD2 assemble as a cohesive structural unit regulated by intermittent associations with pacsin2 and EHBP1. These coats can flatten and curve to enable lipid traffic, signaling, and changes to the surface area of the cell. Nature Publishing Group UK 2022-11-24 /pmc/articles/PMC9700719/ /pubmed/36433988 http://dx.doi.org/10.1038/s41467-022-34958-3 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022 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
Matthaeus, Claudia
Sochacki, Kem A.
Dickey, Andrea M.
Puchkov, Dmytro
Haucke, Volker
Lehmann, Martin
Taraska, Justin W.
The molecular organization of differentially curved caveolae indicates bendable structural units at the plasma membrane
title The molecular organization of differentially curved caveolae indicates bendable structural units at the plasma membrane
title_full The molecular organization of differentially curved caveolae indicates bendable structural units at the plasma membrane
title_fullStr The molecular organization of differentially curved caveolae indicates bendable structural units at the plasma membrane
title_full_unstemmed The molecular organization of differentially curved caveolae indicates bendable structural units at the plasma membrane
title_short The molecular organization of differentially curved caveolae indicates bendable structural units at the plasma membrane
title_sort molecular organization of differentially curved caveolae indicates bendable structural units at the plasma membrane
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700719/
https://www.ncbi.nlm.nih.gov/pubmed/36433988
http://dx.doi.org/10.1038/s41467-022-34958-3
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