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Annexins induce curvature on free-edge membranes displaying distinct morphologies

Annexins are a family of proteins characterized by their ability to bind anionic membranes in response to Ca(2+)-activation. They are involved in a multitude of cellular functions including vesiculation and membrane repair. Here, we investigate the effect of nine annexins (ANXA1-ANXA7, ANXA11, ANXA1...

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Autores principales: Boye, Theresa Louise, Jeppesen, Jonas Camillus, Maeda, Kenji, Pezeshkian, Weria, Solovyeva, Vita, Nylandsted, Jesper, Simonsen, Adam Cohen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037701/
https://www.ncbi.nlm.nih.gov/pubmed/29985397
http://dx.doi.org/10.1038/s41598-018-28481-z
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author Boye, Theresa Louise
Jeppesen, Jonas Camillus
Maeda, Kenji
Pezeshkian, Weria
Solovyeva, Vita
Nylandsted, Jesper
Simonsen, Adam Cohen
author_facet Boye, Theresa Louise
Jeppesen, Jonas Camillus
Maeda, Kenji
Pezeshkian, Weria
Solovyeva, Vita
Nylandsted, Jesper
Simonsen, Adam Cohen
author_sort Boye, Theresa Louise
collection PubMed
description Annexins are a family of proteins characterized by their ability to bind anionic membranes in response to Ca(2+)-activation. They are involved in a multitude of cellular functions including vesiculation and membrane repair. Here, we investigate the effect of nine annexins (ANXA1-ANXA7, ANXA11, ANXA13) on negatively charged double supported membrane patches with free edges. We find that annexin members can be classified according to the membrane morphology they induce and matching a dendrogam of the annexin family based on full amino acid sequences. ANXA1 and ANXA2 induce membrane folding and blebbing initiated from membrane structural defects inside patches while ANXA6 induces membrane folding originating both from defects and from the membrane edges. ANXA4 and ANXA5 induce cooperative roll-up of the membrane starting from free edges, producing large rolls. In contrast, ANXA3 and ANXA13 roll the membrane in a fragmented manner producing multiple thin rolls. In addition to rolling, ANXA7 and ANXA11 are characterized by their ability to form fluid lenses localized between the membrane leaflets. A shared feature necessary for generating these morphologies is the ability to induce membrane curvature on free edged anionic membranes. Consequently, induction of membrane curvature may be a significant property of the annexin protein family that is important for their function.
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spelling pubmed-60377012018-07-12 Annexins induce curvature on free-edge membranes displaying distinct morphologies Boye, Theresa Louise Jeppesen, Jonas Camillus Maeda, Kenji Pezeshkian, Weria Solovyeva, Vita Nylandsted, Jesper Simonsen, Adam Cohen Sci Rep Article Annexins are a family of proteins characterized by their ability to bind anionic membranes in response to Ca(2+)-activation. They are involved in a multitude of cellular functions including vesiculation and membrane repair. Here, we investigate the effect of nine annexins (ANXA1-ANXA7, ANXA11, ANXA13) on negatively charged double supported membrane patches with free edges. We find that annexin members can be classified according to the membrane morphology they induce and matching a dendrogam of the annexin family based on full amino acid sequences. ANXA1 and ANXA2 induce membrane folding and blebbing initiated from membrane structural defects inside patches while ANXA6 induces membrane folding originating both from defects and from the membrane edges. ANXA4 and ANXA5 induce cooperative roll-up of the membrane starting from free edges, producing large rolls. In contrast, ANXA3 and ANXA13 roll the membrane in a fragmented manner producing multiple thin rolls. In addition to rolling, ANXA7 and ANXA11 are characterized by their ability to form fluid lenses localized between the membrane leaflets. A shared feature necessary for generating these morphologies is the ability to induce membrane curvature on free edged anionic membranes. Consequently, induction of membrane curvature may be a significant property of the annexin protein family that is important for their function. Nature Publishing Group UK 2018-07-09 /pmc/articles/PMC6037701/ /pubmed/29985397 http://dx.doi.org/10.1038/s41598-018-28481-z 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
Boye, Theresa Louise
Jeppesen, Jonas Camillus
Maeda, Kenji
Pezeshkian, Weria
Solovyeva, Vita
Nylandsted, Jesper
Simonsen, Adam Cohen
Annexins induce curvature on free-edge membranes displaying distinct morphologies
title Annexins induce curvature on free-edge membranes displaying distinct morphologies
title_full Annexins induce curvature on free-edge membranes displaying distinct morphologies
title_fullStr Annexins induce curvature on free-edge membranes displaying distinct morphologies
title_full_unstemmed Annexins induce curvature on free-edge membranes displaying distinct morphologies
title_short Annexins induce curvature on free-edge membranes displaying distinct morphologies
title_sort annexins induce curvature on free-edge membranes displaying distinct morphologies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037701/
https://www.ncbi.nlm.nih.gov/pubmed/29985397
http://dx.doi.org/10.1038/s41598-018-28481-z
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