Cargando…

Reconstitution of Membrane Proteins into Model Membranes: Seeking Better Ways to Retain Protein Activities

The function of any given biological membrane is determined largely by the specific set of integral membrane proteins embedded in it, and the peripheral membrane proteins attached to the membrane surface. The activity of these proteins, in turn, can be modulated by the phospholipid composition of th...

Descripción completa

Detalles Bibliográficos
Autores principales: Shen, Hsin-Hui, Lithgow, Trevor, Martin, Lisandra L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3565336/
https://www.ncbi.nlm.nih.gov/pubmed/23344058
http://dx.doi.org/10.3390/ijms14011589
_version_ 1782258444584091648
author Shen, Hsin-Hui
Lithgow, Trevor
Martin, Lisandra L.
author_facet Shen, Hsin-Hui
Lithgow, Trevor
Martin, Lisandra L.
author_sort Shen, Hsin-Hui
collection PubMed
description The function of any given biological membrane is determined largely by the specific set of integral membrane proteins embedded in it, and the peripheral membrane proteins attached to the membrane surface. The activity of these proteins, in turn, can be modulated by the phospholipid composition of the membrane. The reconstitution of membrane proteins into a model membrane allows investigation of individual features and activities of a given cell membrane component. However, the activity of membrane proteins is often difficult to sustain following reconstitution, since the composition of the model phospholipid bilayer differs from that of the native cell membrane. This review will discuss the reconstitution of membrane protein activities in four different types of model membrane—monolayers, supported lipid bilayers, liposomes and nanodiscs, comparing their advantages in membrane protein reconstitution. Variation in the surrounding model environments for these four different types of membrane layer can affect the three-dimensional structure of reconstituted proteins and may possibly lead to loss of the proteins activity. We also discuss examples where the same membrane proteins have been successfully reconstituted into two or more model membrane systems with comparison of the observed activity in each system. Understanding of the behavioral changes for proteins in model membrane systems after membrane reconstitution is often a prerequisite to protein research. It is essential to find better solutions for retaining membrane protein activities for measurement and characterization in vitro.
format Online
Article
Text
id pubmed-3565336
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-35653362013-03-13 Reconstitution of Membrane Proteins into Model Membranes: Seeking Better Ways to Retain Protein Activities Shen, Hsin-Hui Lithgow, Trevor Martin, Lisandra L. Int J Mol Sci Review The function of any given biological membrane is determined largely by the specific set of integral membrane proteins embedded in it, and the peripheral membrane proteins attached to the membrane surface. The activity of these proteins, in turn, can be modulated by the phospholipid composition of the membrane. The reconstitution of membrane proteins into a model membrane allows investigation of individual features and activities of a given cell membrane component. However, the activity of membrane proteins is often difficult to sustain following reconstitution, since the composition of the model phospholipid bilayer differs from that of the native cell membrane. This review will discuss the reconstitution of membrane protein activities in four different types of model membrane—monolayers, supported lipid bilayers, liposomes and nanodiscs, comparing their advantages in membrane protein reconstitution. Variation in the surrounding model environments for these four different types of membrane layer can affect the three-dimensional structure of reconstituted proteins and may possibly lead to loss of the proteins activity. We also discuss examples where the same membrane proteins have been successfully reconstituted into two or more model membrane systems with comparison of the observed activity in each system. Understanding of the behavioral changes for proteins in model membrane systems after membrane reconstitution is often a prerequisite to protein research. It is essential to find better solutions for retaining membrane protein activities for measurement and characterization in vitro. MDPI 2013-01-14 /pmc/articles/PMC3565336/ /pubmed/23344058 http://dx.doi.org/10.3390/ijms14011589 Text en © 2013 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Shen, Hsin-Hui
Lithgow, Trevor
Martin, Lisandra L.
Reconstitution of Membrane Proteins into Model Membranes: Seeking Better Ways to Retain Protein Activities
title Reconstitution of Membrane Proteins into Model Membranes: Seeking Better Ways to Retain Protein Activities
title_full Reconstitution of Membrane Proteins into Model Membranes: Seeking Better Ways to Retain Protein Activities
title_fullStr Reconstitution of Membrane Proteins into Model Membranes: Seeking Better Ways to Retain Protein Activities
title_full_unstemmed Reconstitution of Membrane Proteins into Model Membranes: Seeking Better Ways to Retain Protein Activities
title_short Reconstitution of Membrane Proteins into Model Membranes: Seeking Better Ways to Retain Protein Activities
title_sort reconstitution of membrane proteins into model membranes: seeking better ways to retain protein activities
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3565336/
https://www.ncbi.nlm.nih.gov/pubmed/23344058
http://dx.doi.org/10.3390/ijms14011589
work_keys_str_mv AT shenhsinhui reconstitutionofmembraneproteinsintomodelmembranesseekingbetterwaystoretainproteinactivities
AT lithgowtrevor reconstitutionofmembraneproteinsintomodelmembranesseekingbetterwaystoretainproteinactivities
AT martinlisandral reconstitutionofmembraneproteinsintomodelmembranesseekingbetterwaystoretainproteinactivities