Molecular modeling and simulation of membrane lipid-mediated effects on GPCRs

S. K. Sadiq, R. Guixà-González, E. Dainese, M. Pastor, G. De Fabritiis, J. Selent

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

Functioning of G protein-coupled receptors (GPCRs) is tightly linked to the membrane environment, but a molecular level understanding of the modulation of GPCR by membrane lipids is not available. However, specific receptor-lipid interactions as well as unspecific effects mediated by the bulk properties of the membrane (thickness, curvature, etc.) have been proposed to be key regulators of GPCR modulation. In this review, we examine computational efforts made towards modeling and simulation of (i) the complex behavior of membrane lipids, (ii) membrane lipid-GPCR interactions as well as membrane lipid-mediated effects on GPCRs and (iii) GPCR oligomerization in a native-like membrane environment. We propose that, from the perspective of computational modeling, all three of these components need to be addressed in order to achieve a deeper understanding of GPCR functioning. Presently, we are able to simulate numerous lipid properties applying advanced computational techniques, although some barriers, such as the time-length of these simulations, need to be overcome. Implementing three-dimensional structures of GPCRs in such validated membrane systems can give novel insights in membrane-dependent receptor modulation and formation of higher order receptor complexes. Finally, more realistic GPCR-membrane models would provide a very useful tool in studying receptor behavior and its modulation by small drug-like ligands, a relevant issue for drug discovery.

Original languageEnglish
Pages (from-to)22-38
Number of pages17
JournalCurrent Medicinal Chemistry
Volume20
Issue number1
DOIs
Publication statusPublished - Jan 2013

Fingerprint

Molecular modeling
Membrane Lipids
G-Protein-Coupled Receptors
Membranes
Modulation
Lipids
Oligomerization
Drug Discovery
Ligands

Keywords

  • G protein-coupled receptor
  • GPCR regulation
  • Hydrophobic mismatch
  • Lipid bilayer
  • Molecular dynamics
  • Oligomerization

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology

Cite this

Sadiq, S. K., Guixà-González, R., Dainese, E., Pastor, M., De Fabritiis, G., & Selent, J. (2013). Molecular modeling and simulation of membrane lipid-mediated effects on GPCRs. Current Medicinal Chemistry, 20(1), 22-38. https://doi.org/10.2174/09298673130104

Molecular modeling and simulation of membrane lipid-mediated effects on GPCRs. / Sadiq, S. K.; Guixà-González, R.; Dainese, E.; Pastor, M.; De Fabritiis, G.; Selent, J.

In: Current Medicinal Chemistry, Vol. 20, No. 1, 01.2013, p. 22-38.

Research output: Contribution to journalArticle

Sadiq, SK, Guixà-González, R, Dainese, E, Pastor, M, De Fabritiis, G & Selent, J 2013, 'Molecular modeling and simulation of membrane lipid-mediated effects on GPCRs', Current Medicinal Chemistry, vol. 20, no. 1, pp. 22-38. https://doi.org/10.2174/09298673130104
Sadiq SK, Guixà-González R, Dainese E, Pastor M, De Fabritiis G, Selent J. Molecular modeling and simulation of membrane lipid-mediated effects on GPCRs. Current Medicinal Chemistry. 2013 Jan;20(1):22-38. https://doi.org/10.2174/09298673130104
Sadiq, S. K. ; Guixà-González, R. ; Dainese, E. ; Pastor, M. ; De Fabritiis, G. ; Selent, J. / Molecular modeling and simulation of membrane lipid-mediated effects on GPCRs. In: Current Medicinal Chemistry. 2013 ; Vol. 20, No. 1. pp. 22-38.
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