Cargando…

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)...

Descripción completa

Detalles Bibliográficos
Autores principales: Paulowski, Laura, Donoghue, Annemarie, Nehls, Christian, Groth, Sabrina, Koistinen, Max, Hagge, Sven O., Böhling, Arne, Winterhalter, Mathias, Gutsmann, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
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
_version_ 1783562998481158144
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
work_keys_str_mv AT paulowskilaura thebeautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT donoghueannemarie thebeautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT nehlschristian thebeautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT grothsabrina thebeautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT koistinenmax thebeautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT haggesveno thebeautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT bohlingarne thebeautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT winterhaltermathias thebeautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT gutsmannthomas thebeautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT paulowskilaura beautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT donoghueannemarie beautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT nehlschristian beautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT grothsabrina beautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT koistinenmax beautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT haggesveno beautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT bohlingarne beautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT winterhaltermathias beautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria
AT gutsmannthomas beautyofasymmetricmembranesreconstitutionoftheoutermembraneofgramnegativebacteria