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Reduced level of docosahexaenoic acid shifts GPCR neuroreceptors to less ordered membrane regions
M. Javanainen, G. Enkavi, R. Guixà-Gonzaléz, W. Kulig, H. Martinez-Seara, I. Levental, I. Vattulainen,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2005
Free Medical Journals
od 2005
Public Library of Science (PLoS)
od 2005
PubMed Central
od 2005
Europe PubMed Central
od 2005
ProQuest Central
od 2005-06-01
Open Access Digital Library
od 2005-01-01
Open Access Digital Library
od 2005-01-01
Open Access Digital Library
od 2005-06-01
Medline Complete (EBSCOhost)
od 2005-06-01
Health & Medicine (ProQuest)
od 2005-06-01
ROAD: Directory of Open Access Scholarly Resources
od 2005
- MeSH
- cholesterol metabolismus MeSH
- konformace proteinů MeSH
- kyseliny dokosahexaenové chemie metabolismus MeSH
- lidé MeSH
- membránové mikrodomény chemie metabolismus MeSH
- membránové proteiny chemie metabolismus MeSH
- modely neurologické MeSH
- molekulární modely MeSH
- mozek metabolismus MeSH
- nenasycené mastné kyseliny metabolismus MeSH
- nervové receptory chemie metabolismus MeSH
- počítačová simulace MeSH
- receptor adenosinový A2A chemie metabolismus MeSH
- receptory spřažené s G-proteiny chemie metabolismus MeSH
- signální transdukce MeSH
- termodynamika MeSH
- výpočetní biologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
G protein-coupled receptors (GPCRs) control cellular signaling and responses. Many of these GPCRs are modulated by cholesterol and polyunsaturated fatty acids (PUFAs) which have been shown to co-exist with saturated lipids in ordered membrane domains. However, the lipid compositions of such domains extracted from the brain cortex tissue of individuals suffering from GPCR-associated neurological disorders show drastically lowered levels of PUFAs. Here, using free energy techniques and multiscale simulations of numerous membrane proteins, we show that the presence of the PUFA DHA helps helical multi-pass proteins such as GPCRs partition into ordered membrane domains. The mechanism is based on hybrid lipids, whose PUFA chains coat the rough protein surface, while the saturated chains face the raft environment, thus minimizing perturbations therein. Our findings suggest that the reduction of GPCR partitioning to their native ordered environments due to PUFA depletion might affect the function of these receptors in numerous neurodegenerative diseases, where the membrane PUFA levels in the brain are decreased. We hope that this work inspires experimental studies on the connection between membrane PUFA levels and GPCR signaling.
Citace poskytuje Crossref.org
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- $a G protein-coupled receptors (GPCRs) control cellular signaling and responses. Many of these GPCRs are modulated by cholesterol and polyunsaturated fatty acids (PUFAs) which have been shown to co-exist with saturated lipids in ordered membrane domains. However, the lipid compositions of such domains extracted from the brain cortex tissue of individuals suffering from GPCR-associated neurological disorders show drastically lowered levels of PUFAs. Here, using free energy techniques and multiscale simulations of numerous membrane proteins, we show that the presence of the PUFA DHA helps helical multi-pass proteins such as GPCRs partition into ordered membrane domains. The mechanism is based on hybrid lipids, whose PUFA chains coat the rough protein surface, while the saturated chains face the raft environment, thus minimizing perturbations therein. Our findings suggest that the reduction of GPCR partitioning to their native ordered environments due to PUFA depletion might affect the function of these receptors in numerous neurodegenerative diseases, where the membrane PUFA levels in the brain are decreased. We hope that this work inspires experimental studies on the connection between membrane PUFA levels and GPCR signaling.
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