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Beating Vesicles: Encapsulated Protein Oscillations Cause Dynamic Membrane Deformations

The bacterial Min protein system was encapsulated in giant unilamellar vesicles (GUVs). Using confocal fluorescence microscopy, we identified several distinct modes of spatiotemporal patterns inside spherical GUVs. For osmotically deflated GUVs, the vesicle shape actively changed in concert with the...

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Autores principales: Litschel, Thomas, Ramm, Beatrice, Maas, Roel, Heymann, Michael, Schwille, Petra
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/PMC6391971/
https://www.ncbi.nlm.nih.gov/pubmed/30270475
http://dx.doi.org/10.1002/anie.201808750
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author Litschel, Thomas
Ramm, Beatrice
Maas, Roel
Heymann, Michael
Schwille, Petra
author_facet Litschel, Thomas
Ramm, Beatrice
Maas, Roel
Heymann, Michael
Schwille, Petra
author_sort Litschel, Thomas
collection PubMed
description The bacterial Min protein system was encapsulated in giant unilamellar vesicles (GUVs). Using confocal fluorescence microscopy, we identified several distinct modes of spatiotemporal patterns inside spherical GUVs. For osmotically deflated GUVs, the vesicle shape actively changed in concert with the Min oscillations. The periodic relocation of Min proteins from the vesicle lumen to the membrane and back is accompanied by drastic changes in the mechanical properties of the lipid bilayer. In particular, two types of oscillating membrane‐shape changes are highlighted: 1) GUVs that repeatedly undergo fission into two connected compartments and fusion of these compartments back into a dumbbell shape and 2) GUVs that show periodic budding and subsequent merging of the buds with the mother vesicle, accompanied by an overall shape change of the vesicle reminiscent of a bouncing ball. These findings demonstrate how reaction–diffusion‐based protein self‐organization can directly yield visible mechanical effects on membrane compartments, even up to autonomous division, without the need for coupling to cytoskeletal elements.
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spelling pubmed-63919712019-03-07 Beating Vesicles: Encapsulated Protein Oscillations Cause Dynamic Membrane Deformations Litschel, Thomas Ramm, Beatrice Maas, Roel Heymann, Michael Schwille, Petra Angew Chem Int Ed Engl Communications The bacterial Min protein system was encapsulated in giant unilamellar vesicles (GUVs). Using confocal fluorescence microscopy, we identified several distinct modes of spatiotemporal patterns inside spherical GUVs. For osmotically deflated GUVs, the vesicle shape actively changed in concert with the Min oscillations. The periodic relocation of Min proteins from the vesicle lumen to the membrane and back is accompanied by drastic changes in the mechanical properties of the lipid bilayer. In particular, two types of oscillating membrane‐shape changes are highlighted: 1) GUVs that repeatedly undergo fission into two connected compartments and fusion of these compartments back into a dumbbell shape and 2) GUVs that show periodic budding and subsequent merging of the buds with the mother vesicle, accompanied by an overall shape change of the vesicle reminiscent of a bouncing ball. These findings demonstrate how reaction–diffusion‐based protein self‐organization can directly yield visible mechanical effects on membrane compartments, even up to autonomous division, without the need for coupling to cytoskeletal elements. John Wiley and Sons Inc. 2018-11-20 2018-12-10 /pmc/articles/PMC6391971/ /pubmed/30270475 http://dx.doi.org/10.1002/anie.201808750 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Litschel, Thomas
Ramm, Beatrice
Maas, Roel
Heymann, Michael
Schwille, Petra
Beating Vesicles: Encapsulated Protein Oscillations Cause Dynamic Membrane Deformations
title Beating Vesicles: Encapsulated Protein Oscillations Cause Dynamic Membrane Deformations
title_full Beating Vesicles: Encapsulated Protein Oscillations Cause Dynamic Membrane Deformations
title_fullStr Beating Vesicles: Encapsulated Protein Oscillations Cause Dynamic Membrane Deformations
title_full_unstemmed Beating Vesicles: Encapsulated Protein Oscillations Cause Dynamic Membrane Deformations
title_short Beating Vesicles: Encapsulated Protein Oscillations Cause Dynamic Membrane Deformations
title_sort beating vesicles: encapsulated protein oscillations cause dynamic membrane deformations
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391971/
https://www.ncbi.nlm.nih.gov/pubmed/30270475
http://dx.doi.org/10.1002/anie.201808750
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