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Dynamic Structure Formation of Peripheral Membrane Proteins

Using coarse-grained membrane simulations we show here that peripheral membrane proteins can form a multitude of higher-order structures due to membrane-mediated interactions. Peripheral membrane proteins characteristically perturb the lipid bilayer in their vicinity which supports the formation of...

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Detalles Bibliográficos
Autores principales: Morozova, Diana, Guigas, Gernot, Weiss, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121687/
https://www.ncbi.nlm.nih.gov/pubmed/21731477
http://dx.doi.org/10.1371/journal.pcbi.1002067
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author Morozova, Diana
Guigas, Gernot
Weiss, Matthias
author_facet Morozova, Diana
Guigas, Gernot
Weiss, Matthias
author_sort Morozova, Diana
collection PubMed
description Using coarse-grained membrane simulations we show here that peripheral membrane proteins can form a multitude of higher-order structures due to membrane-mediated interactions. Peripheral membrane proteins characteristically perturb the lipid bilayer in their vicinity which supports the formation of protein assemblies not only within the same but surprisingly also across opposing leaflets of a bilayer. In addition, we also observed the formation of lipid-protein domains on heteregeneous membranes. The clustering ability of proteins, as quantified via the potential of mean force, is enhanced when radius and hydrophobic penetration depth of the proteins increases. Based on our data, we propose that membrane-mediated cluster formation of peripheral proteins supports protein assembly in vivo and hence may play a pivotal role in the formation of templates for signaling cascades and in the emergence of transport intermediates in the secretory pathway.
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spelling pubmed-31216872011-06-30 Dynamic Structure Formation of Peripheral Membrane Proteins Morozova, Diana Guigas, Gernot Weiss, Matthias PLoS Comput Biol Research Article Using coarse-grained membrane simulations we show here that peripheral membrane proteins can form a multitude of higher-order structures due to membrane-mediated interactions. Peripheral membrane proteins characteristically perturb the lipid bilayer in their vicinity which supports the formation of protein assemblies not only within the same but surprisingly also across opposing leaflets of a bilayer. In addition, we also observed the formation of lipid-protein domains on heteregeneous membranes. The clustering ability of proteins, as quantified via the potential of mean force, is enhanced when radius and hydrophobic penetration depth of the proteins increases. Based on our data, we propose that membrane-mediated cluster formation of peripheral proteins supports protein assembly in vivo and hence may play a pivotal role in the formation of templates for signaling cascades and in the emergence of transport intermediates in the secretory pathway. Public Library of Science 2011-06-23 /pmc/articles/PMC3121687/ /pubmed/21731477 http://dx.doi.org/10.1371/journal.pcbi.1002067 Text en Morozova, et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Morozova, Diana
Guigas, Gernot
Weiss, Matthias
Dynamic Structure Formation of Peripheral Membrane Proteins
title Dynamic Structure Formation of Peripheral Membrane Proteins
title_full Dynamic Structure Formation of Peripheral Membrane Proteins
title_fullStr Dynamic Structure Formation of Peripheral Membrane Proteins
title_full_unstemmed Dynamic Structure Formation of Peripheral Membrane Proteins
title_short Dynamic Structure Formation of Peripheral Membrane Proteins
title_sort dynamic structure formation of peripheral membrane proteins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121687/
https://www.ncbi.nlm.nih.gov/pubmed/21731477
http://dx.doi.org/10.1371/journal.pcbi.1002067
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