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The Beauty of Asymmetric Membranes: Reconstitution of the Outer Membrane of Gram-Negative Bacteria
The architecture of the lipid matrix of the outer membrane of Gram-negative bacteria is extremely asymmetric: Whereas the inner leaflet is composed of a phospholipid mixture, the outer leaflet is built up by glycolipids. For most Gram-negative species, these glycolipids are lipopolysaccharides (LPS)...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381204/ https://www.ncbi.nlm.nih.gov/pubmed/32766244 http://dx.doi.org/10.3389/fcell.2020.00586 |
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author | Paulowski, Laura Donoghue, Annemarie Nehls, Christian Groth, Sabrina Koistinen, Max Hagge, Sven O. Böhling, Arne Winterhalter, Mathias Gutsmann, Thomas |
author_facet | Paulowski, Laura Donoghue, Annemarie Nehls, Christian Groth, Sabrina Koistinen, Max Hagge, Sven O. Böhling, Arne Winterhalter, Mathias Gutsmann, Thomas |
author_sort | Paulowski, Laura |
collection | PubMed |
description | The architecture of the lipid matrix of the outer membrane of Gram-negative bacteria is extremely asymmetric: Whereas the inner leaflet is composed of a phospholipid mixture, the outer leaflet is built up by glycolipids. For most Gram-negative species, these glycolipids are lipopolysaccharides (LPS), for a few species, however, glycosphingolipids. We demonstrate experimental approaches for the reconstitution of these asymmetric membranes as (i) solid supported membranes prepared by the Langmuir-Blodgett technique, (ii) planar lipid bilayers prepared by the Montal-Mueller technique, and (iii) giant unilamellar vesicles (GUVs) prepared by the phase transfer method. The asymmetric GUVs (aGUVs) composed of LPS on one leaflet are shown for the first time. They are characterized with respect to their phase behavior, flip-flop of lipids and their usability to investigate the interaction with membrane active peptides or proteins. For the antimicrobial peptide LL-32 and for the bacterial porin OmpF the specificity of the interaction with asymmetric membranes is shown. The three reconstitution systems are compared with respect to their usability to investigate domain formation and interactions with peptides and proteins. |
format | Online Article Text |
id | pubmed-7381204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73812042020-08-05 The Beauty of Asymmetric Membranes: Reconstitution of the Outer Membrane of Gram-Negative Bacteria Paulowski, Laura Donoghue, Annemarie Nehls, Christian Groth, Sabrina Koistinen, Max Hagge, Sven O. Böhling, Arne Winterhalter, Mathias Gutsmann, Thomas Front Cell Dev Biol Cell and Developmental Biology The architecture of the lipid matrix of the outer membrane of Gram-negative bacteria is extremely asymmetric: Whereas the inner leaflet is composed of a phospholipid mixture, the outer leaflet is built up by glycolipids. For most Gram-negative species, these glycolipids are lipopolysaccharides (LPS), for a few species, however, glycosphingolipids. We demonstrate experimental approaches for the reconstitution of these asymmetric membranes as (i) solid supported membranes prepared by the Langmuir-Blodgett technique, (ii) planar lipid bilayers prepared by the Montal-Mueller technique, and (iii) giant unilamellar vesicles (GUVs) prepared by the phase transfer method. The asymmetric GUVs (aGUVs) composed of LPS on one leaflet are shown for the first time. They are characterized with respect to their phase behavior, flip-flop of lipids and their usability to investigate the interaction with membrane active peptides or proteins. For the antimicrobial peptide LL-32 and for the bacterial porin OmpF the specificity of the interaction with asymmetric membranes is shown. The three reconstitution systems are compared with respect to their usability to investigate domain formation and interactions with peptides and proteins. Frontiers Media S.A. 2020-07-14 /pmc/articles/PMC7381204/ /pubmed/32766244 http://dx.doi.org/10.3389/fcell.2020.00586 Text en Copyright © 2020 Paulowski, Donoghue, Nehls, Groth, Koistinen, Hagge, Böhling, Winterhalter and Gutsmann. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Paulowski, Laura Donoghue, Annemarie Nehls, Christian Groth, Sabrina Koistinen, Max Hagge, Sven O. Böhling, Arne Winterhalter, Mathias Gutsmann, Thomas The Beauty of Asymmetric Membranes: Reconstitution of the Outer Membrane of Gram-Negative Bacteria |
title | The Beauty of Asymmetric Membranes: Reconstitution of the Outer Membrane of Gram-Negative Bacteria |
title_full | The Beauty of Asymmetric Membranes: Reconstitution of the Outer Membrane of Gram-Negative Bacteria |
title_fullStr | The Beauty of Asymmetric Membranes: Reconstitution of the Outer Membrane of Gram-Negative Bacteria |
title_full_unstemmed | The Beauty of Asymmetric Membranes: Reconstitution of the Outer Membrane of Gram-Negative Bacteria |
title_short | The Beauty of Asymmetric Membranes: Reconstitution of the Outer Membrane of Gram-Negative Bacteria |
title_sort | beauty of asymmetric membranes: reconstitution of the outer membrane of gram-negative bacteria |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381204/ https://www.ncbi.nlm.nih.gov/pubmed/32766244 http://dx.doi.org/10.3389/fcell.2020.00586 |
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