The integrin receptor in biologically relevant bilayers: insights from molecular dynamics simulations

Integrins are heterodimeric (αβ) cell surface receptors that are potential therapeutic targets for a number of diseases. Despite the existence of structural data for all parts of integrins, the structure of the complete integrin receptor is still not available. We have used available structural data...

Full description

Bibliographic Details
Main Authors: Kalli, A, Rog, T, Vattulainen, I, Campbell, I, Sansom, M
Format: Journal article
Published: Springer US 2016
_version_ 1797081415795343360
author Kalli, A
Rog, T
Vattulainen, I
Campbell, I
Sansom, M
author_facet Kalli, A
Rog, T
Vattulainen, I
Campbell, I
Sansom, M
author_sort Kalli, A
collection OXFORD
description Integrins are heterodimeric (αβ) cell surface receptors that are potential therapeutic targets for a number of diseases. Despite the existence of structural data for all parts of integrins, the structure of the complete integrin receptor is still not available. We have used available structural data to construct a model of the complete integrin receptor in complex with talin F2-F3 domain. It has been shown that the interactions of integrins with their lipid environment are crucial for their function but details of the integrin/lipid interactions remain elusive. In this study an integrin/talin complex was inserted in biologically relevant bilayers that resemble the cell plasma membrane containing zwitterionic and charged phospholipids, cholesterol and sphingolipids to study the dynamics of the integrin receptor and its effect in bilayer structure and dynamics. The results of this study demonstrate the dynamic nature of the integrin receptor and suggest that the presence of the integrin receptor alters the lipid organization between the two leaflets of the bilayer. In particular, our results suggest elevated density of cholesterol and of phosphatidyl serine lipids around the integrin/talin complex and a slowing-down of lipids in an annulus of ~30 Å around the protein due to interactions between the lipids and the integrin/talin F2-F3 complex. This may in part regulate the interactions of integrins with other related proteins or integrin clustering thus facilitating signal transduction across cell membranes
first_indexed 2024-03-07T01:14:08Z
format Journal article
id oxford-uuid:8e122851-600d-490c-8f7b-86803bed9b81
institution University of Oxford
last_indexed 2024-03-07T01:14:08Z
publishDate 2016
publisher Springer US
record_format dspace
spelling oxford-uuid:8e122851-600d-490c-8f7b-86803bed9b812022-03-26T22:55:12ZThe integrin receptor in biologically relevant bilayers: insights from molecular dynamics simulationsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:8e122851-600d-490c-8f7b-86803bed9b81Symplectic Elements at OxfordSpringer US2016Kalli, ARog, TVattulainen, ICampbell, ISansom, MIntegrins are heterodimeric (αβ) cell surface receptors that are potential therapeutic targets for a number of diseases. Despite the existence of structural data for all parts of integrins, the structure of the complete integrin receptor is still not available. We have used available structural data to construct a model of the complete integrin receptor in complex with talin F2-F3 domain. It has been shown that the interactions of integrins with their lipid environment are crucial for their function but details of the integrin/lipid interactions remain elusive. In this study an integrin/talin complex was inserted in biologically relevant bilayers that resemble the cell plasma membrane containing zwitterionic and charged phospholipids, cholesterol and sphingolipids to study the dynamics of the integrin receptor and its effect in bilayer structure and dynamics. The results of this study demonstrate the dynamic nature of the integrin receptor and suggest that the presence of the integrin receptor alters the lipid organization between the two leaflets of the bilayer. In particular, our results suggest elevated density of cholesterol and of phosphatidyl serine lipids around the integrin/talin complex and a slowing-down of lipids in an annulus of ~30 Å around the protein due to interactions between the lipids and the integrin/talin F2-F3 complex. This may in part regulate the interactions of integrins with other related proteins or integrin clustering thus facilitating signal transduction across cell membranes
spellingShingle Kalli, A
Rog, T
Vattulainen, I
Campbell, I
Sansom, M
The integrin receptor in biologically relevant bilayers: insights from molecular dynamics simulations
title The integrin receptor in biologically relevant bilayers: insights from molecular dynamics simulations
title_full The integrin receptor in biologically relevant bilayers: insights from molecular dynamics simulations
title_fullStr The integrin receptor in biologically relevant bilayers: insights from molecular dynamics simulations
title_full_unstemmed The integrin receptor in biologically relevant bilayers: insights from molecular dynamics simulations
title_short The integrin receptor in biologically relevant bilayers: insights from molecular dynamics simulations
title_sort integrin receptor in biologically relevant bilayers insights from molecular dynamics simulations
work_keys_str_mv AT kallia theintegrinreceptorinbiologicallyrelevantbilayersinsightsfrommoleculardynamicssimulations
AT rogt theintegrinreceptorinbiologicallyrelevantbilayersinsightsfrommoleculardynamicssimulations
AT vattulaineni theintegrinreceptorinbiologicallyrelevantbilayersinsightsfrommoleculardynamicssimulations
AT campbelli theintegrinreceptorinbiologicallyrelevantbilayersinsightsfrommoleculardynamicssimulations
AT sansomm theintegrinreceptorinbiologicallyrelevantbilayersinsightsfrommoleculardynamicssimulations
AT kallia integrinreceptorinbiologicallyrelevantbilayersinsightsfrommoleculardynamicssimulations
AT rogt integrinreceptorinbiologicallyrelevantbilayersinsightsfrommoleculardynamicssimulations
AT vattulaineni integrinreceptorinbiologicallyrelevantbilayersinsightsfrommoleculardynamicssimulations
AT campbelli integrinreceptorinbiologicallyrelevantbilayersinsightsfrommoleculardynamicssimulations
AT sansomm integrinreceptorinbiologicallyrelevantbilayersinsightsfrommoleculardynamicssimulations