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Roles of G‐protein‐coupled receptor dimerization: From ontogeny to signalling regulation

Open access
Terrillon, Sonia, Bouvier, Michel·2004·EMBO reports

Abstract

The classical idea that G‐protein‐coupled receptors (GPCRs) function as monomeric entities has been unsettled by the emerging concept of GPCR dimerization. Recent findings have indicated not only that many GPCRs exist as homodimers and heterodimers, but also that their oligomeric assembly could have important functional roles. Several studies have shown that dimerization occurs early after biosynthesis, suggesting that it has a primary role in receptor maturation. G‐protein coupling, downstream signalling and regulatory processes such as internalization have also been shown to be influenced by the dimeric nature of the receptors. In addition to raising fundamental questions about GPCR function, the concept of dimerization could be important in the development and screening of drugs that act through this receptor class. In particular, the changes in ligand‐binding and signalling properties that accompany heterodimerization could give rise to an unexpected pharmacological diversity that would need to be considered.

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Metadata

Authors
Terrillon, S., & Bouvier, M.
Venue
EMBO reports
Published
2004-01
Volume
5
Issue
1
Pages
30-34
ISSN
  • 1469-221X (ISSN-L)
  • 1469-3178
OpenAlex
W2079052124
Cited by
683
References
1
FWCI
22.52
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Roles of G‐protein‐coupled receptor dimerization: From ontogeny to signalling regulation. https://app.cochat.ai/papers/10.1038/sj.embor.7400052
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Terrillon, S., & Bouvier, M. (2004). Roles of G‐protein‐coupled receptor dimerization: From ontogeny to signalling regulation. EMBO reports. https://doi.org/10.1038/sj.embor.7400052

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.