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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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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. |
format | Online Article Text |
id | pubmed-6391971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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