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Area Increase and Budding in Giant Vesicles Triggered by Light: Behind the Scene

Biomembranes are constantly remodeled and in cells, these processes are controlled and modulated by an assortment of membrane proteins. Here, it is shown that such remodeling can also be induced by photoresponsive molecules. The morphological control of giant vesicles in the presence of a water‐solu...

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Autores principales: Georgiev, Vasil N., Grafmüller, Andrea, Bléger, David, Hecht, Stefan, Kunstmann, Sonja, Barbirz, Stefanie, Lipowsky, Reinhard, Dimova, Rumiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096984/
https://www.ncbi.nlm.nih.gov/pubmed/30128249
http://dx.doi.org/10.1002/advs.201800432
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author Georgiev, Vasil N.
Grafmüller, Andrea
Bléger, David
Hecht, Stefan
Kunstmann, Sonja
Barbirz, Stefanie
Lipowsky, Reinhard
Dimova, Rumiana
author_facet Georgiev, Vasil N.
Grafmüller, Andrea
Bléger, David
Hecht, Stefan
Kunstmann, Sonja
Barbirz, Stefanie
Lipowsky, Reinhard
Dimova, Rumiana
author_sort Georgiev, Vasil N.
collection PubMed
description Biomembranes are constantly remodeled and in cells, these processes are controlled and modulated by an assortment of membrane proteins. Here, it is shown that such remodeling can also be induced by photoresponsive molecules. The morphological control of giant vesicles in the presence of a water‐soluble ortho‐tetrafluoroazobenzene photoswitch (F‐azo) is demonstrated and it is shown that the shape transformations are based on an increase in membrane area and generation of spontaneous curvature. The vesicles exhibit budding and the buds can be retracted by using light of a different wavelength. In the presence of F‐azo, the membrane area can increase by more than 5% as assessed from vesicle electrodeformation. To elucidate the underlying molecular mechanism and the partitioning of F‐azo in the membrane, molecular dynamics simulations are employed. Comparison with theoretically calculated shapes reveals that the budded shapes are governed by curvature elasticity, that the spontaneous curvature can be decomposed into a local and a nonlocal contribution, and that the local spontaneous curvature is about 1/(2.5 µm). The results show that exo‐ and endocytotic events can be controlled by light and that these photoinduced processes provide an attractive method to change membrane area and morphology.
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spelling pubmed-60969842018-08-20 Area Increase and Budding in Giant Vesicles Triggered by Light: Behind the Scene Georgiev, Vasil N. Grafmüller, Andrea Bléger, David Hecht, Stefan Kunstmann, Sonja Barbirz, Stefanie Lipowsky, Reinhard Dimova, Rumiana Adv Sci (Weinh) Full Papers Biomembranes are constantly remodeled and in cells, these processes are controlled and modulated by an assortment of membrane proteins. Here, it is shown that such remodeling can also be induced by photoresponsive molecules. The morphological control of giant vesicles in the presence of a water‐soluble ortho‐tetrafluoroazobenzene photoswitch (F‐azo) is demonstrated and it is shown that the shape transformations are based on an increase in membrane area and generation of spontaneous curvature. The vesicles exhibit budding and the buds can be retracted by using light of a different wavelength. In the presence of F‐azo, the membrane area can increase by more than 5% as assessed from vesicle electrodeformation. To elucidate the underlying molecular mechanism and the partitioning of F‐azo in the membrane, molecular dynamics simulations are employed. Comparison with theoretically calculated shapes reveals that the budded shapes are governed by curvature elasticity, that the spontaneous curvature can be decomposed into a local and a nonlocal contribution, and that the local spontaneous curvature is about 1/(2.5 µm). The results show that exo‐ and endocytotic events can be controlled by light and that these photoinduced processes provide an attractive method to change membrane area and morphology. John Wiley and Sons Inc. 2018-06-05 /pmc/articles/PMC6096984/ /pubmed/30128249 http://dx.doi.org/10.1002/advs.201800432 Text en © 2018 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Georgiev, Vasil N.
Grafmüller, Andrea
Bléger, David
Hecht, Stefan
Kunstmann, Sonja
Barbirz, Stefanie
Lipowsky, Reinhard
Dimova, Rumiana
Area Increase and Budding in Giant Vesicles Triggered by Light: Behind the Scene
title Area Increase and Budding in Giant Vesicles Triggered by Light: Behind the Scene
title_full Area Increase and Budding in Giant Vesicles Triggered by Light: Behind the Scene
title_fullStr Area Increase and Budding in Giant Vesicles Triggered by Light: Behind the Scene
title_full_unstemmed Area Increase and Budding in Giant Vesicles Triggered by Light: Behind the Scene
title_short Area Increase and Budding in Giant Vesicles Triggered by Light: Behind the Scene
title_sort area increase and budding in giant vesicles triggered by light: behind the scene
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096984/
https://www.ncbi.nlm.nih.gov/pubmed/30128249
http://dx.doi.org/10.1002/advs.201800432
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