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...
Main Authors: | , , , , |
---|---|
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 |