Cargando…

Biomimetic Models to Investigate Membrane Biophysics Affecting Lipid–Protein Interaction

Biological membranes are highly dynamic in their ability to orchestrate vital mechanisms including cellular protection, organelle compartmentalization, cellular biomechanics, nutrient transport, molecular/enzymatic recognition, and membrane fusion. Controlling lipid composition of different membrane...

Descripción completa

Detalles Bibliográficos
Autores principales: Sarkis, Joe, Vié, Véronique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179690/
https://www.ncbi.nlm.nih.gov/pubmed/32373596
http://dx.doi.org/10.3389/fbioe.2020.00270
_version_ 1783525688931778560
author Sarkis, Joe
Vié, Véronique
author_facet Sarkis, Joe
Vié, Véronique
author_sort Sarkis, Joe
collection PubMed
description Biological membranes are highly dynamic in their ability to orchestrate vital mechanisms including cellular protection, organelle compartmentalization, cellular biomechanics, nutrient transport, molecular/enzymatic recognition, and membrane fusion. Controlling lipid composition of different membranes allows cells to regulate their membrane characteristics, thus modifying their physical properties to permit specific protein interactions and drive structural function (membrane deformation facilitates vesicle budding and fusion) and signal transduction. Yet, how lipids control protein structure and function is still poorly understood and needs systematic investigation. In this review, we explore different in vitro membrane models and summarize our current understanding of the interplay between membrane biophysical properties and lipid–protein interaction, taken as example few proteins involved in muscular activity (dystrophin), digestion and Legionella pneumophila effector protein DrrA. The monolayer model with its movable barriers aims to mimic any membrane deformation while surface pressure modulation imitates lipid packing and membrane curvature changes. It is frequently used to investigate peripheral protein binding to the lipid headgroups. Examples of how lipid lateral pressure modifies protein interaction and organization within the membrane are presented using various biophysical techniques. Interestingly, the shear elasticity and surface viscosity of the monolayer will increase upon specific protein(s) binding, supporting the importance of such mechanical link for membrane stability. The lipid bilayer models such as vesicles are not only used to investigate direct protein binding based on the lipid nature, but more importantly to assess how local membrane curvature (vesicles with different size) influence the binding properties of a protein. Also, supported lipid bilayer model has been used widely to characterize diffusion law of lipids within the bilayer and/or protein/biomolecule binding and diffusion on the membrane. These membrane models continue to elucidate important advances regarding the dynamic properties harmonizing lipid–protein interaction.
format Online
Article
Text
id pubmed-7179690
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-71796902020-05-05 Biomimetic Models to Investigate Membrane Biophysics Affecting Lipid–Protein Interaction Sarkis, Joe Vié, Véronique Front Bioeng Biotechnol Bioengineering and Biotechnology Biological membranes are highly dynamic in their ability to orchestrate vital mechanisms including cellular protection, organelle compartmentalization, cellular biomechanics, nutrient transport, molecular/enzymatic recognition, and membrane fusion. Controlling lipid composition of different membranes allows cells to regulate their membrane characteristics, thus modifying their physical properties to permit specific protein interactions and drive structural function (membrane deformation facilitates vesicle budding and fusion) and signal transduction. Yet, how lipids control protein structure and function is still poorly understood and needs systematic investigation. In this review, we explore different in vitro membrane models and summarize our current understanding of the interplay between membrane biophysical properties and lipid–protein interaction, taken as example few proteins involved in muscular activity (dystrophin), digestion and Legionella pneumophila effector protein DrrA. The monolayer model with its movable barriers aims to mimic any membrane deformation while surface pressure modulation imitates lipid packing and membrane curvature changes. It is frequently used to investigate peripheral protein binding to the lipid headgroups. Examples of how lipid lateral pressure modifies protein interaction and organization within the membrane are presented using various biophysical techniques. Interestingly, the shear elasticity and surface viscosity of the monolayer will increase upon specific protein(s) binding, supporting the importance of such mechanical link for membrane stability. The lipid bilayer models such as vesicles are not only used to investigate direct protein binding based on the lipid nature, but more importantly to assess how local membrane curvature (vesicles with different size) influence the binding properties of a protein. Also, supported lipid bilayer model has been used widely to characterize diffusion law of lipids within the bilayer and/or protein/biomolecule binding and diffusion on the membrane. These membrane models continue to elucidate important advances regarding the dynamic properties harmonizing lipid–protein interaction. Frontiers Media S.A. 2020-04-15 /pmc/articles/PMC7179690/ /pubmed/32373596 http://dx.doi.org/10.3389/fbioe.2020.00270 Text en Copyright © 2020 Sarkis and Vié. 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 Bioengineering and Biotechnology
Sarkis, Joe
Vié, Véronique
Biomimetic Models to Investigate Membrane Biophysics Affecting Lipid–Protein Interaction
title Biomimetic Models to Investigate Membrane Biophysics Affecting Lipid–Protein Interaction
title_full Biomimetic Models to Investigate Membrane Biophysics Affecting Lipid–Protein Interaction
title_fullStr Biomimetic Models to Investigate Membrane Biophysics Affecting Lipid–Protein Interaction
title_full_unstemmed Biomimetic Models to Investigate Membrane Biophysics Affecting Lipid–Protein Interaction
title_short Biomimetic Models to Investigate Membrane Biophysics Affecting Lipid–Protein Interaction
title_sort biomimetic models to investigate membrane biophysics affecting lipid–protein interaction
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179690/
https://www.ncbi.nlm.nih.gov/pubmed/32373596
http://dx.doi.org/10.3389/fbioe.2020.00270
work_keys_str_mv AT sarkisjoe biomimeticmodelstoinvestigatemembranebiophysicsaffectinglipidproteininteraction
AT vieveronique biomimeticmodelstoinvestigatemembranebiophysicsaffectinglipidproteininteraction