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cc-by-nc (c) Gómer Soler, Maricel et al., 2011
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/48611

On the role of G protein-coupled receptors oligomerization

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The existence of a supramolecular organization of the G protein-coupled receptor (GPCR) is now being widely accepted by the scientific community. Indeed, GPCR oligomers may enhance the diversity and performance by which extracellular signals are transferred to the G proteins in the process of receptor transduction, although the mechanism that underlies this phenomenon still remains unsolved. Recently, it has been proposed that a trans-conformational switching model could be the mechanism allowing direct inhibition/activation of receptor activation/inhibition, respectively. Thus, heterotropic receptor-receptor allosteric regulations are behind the GPCR oligomeric function. In this paper we want to revise how GPCR oligomerization impinges on several important receptor functions like biosynthesis, plasma membrane diffusion or velocity, pharmacology and signaling. In particular, the rationale of receptor oligomerization might lie in the need of sensing complex whole cell extracellular signals and translating them into a simple computational model.

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GÓMER SOLER, Maricel, AHERN, Siobhán, FERNÁNDEZ DUEÑAS, Víctor, CIRUELA ALFÉREZ, Francisco. On the role of G protein-coupled receptors oligomerization. _The Open Biology Journal_. 2011. Vol. 4, núm. 1, pàgs. 47-53. [consulta: 21 de gener de 2026]. ISSN: 1874-1967. [Disponible a: https://hdl.handle.net/2445/48611]

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