Literature DB >> 14726257

G-protein coupled receptor oligomerization in neuroendocrine pathways.

Karen M Kroeger1, Kevin D G Pfleger, Karin A Eidne.   

Abstract

Protein-protein interactions are fundamental processes for many biological systems including those involving the superfamily of G-protein coupled receptors (GPCRs). A growing body of biochemical and functional evidence supports the existence of GPCR-GPCR homo- and hetero-oligomers. In particular, hetero-oligomers can display pharmacological and functional properties distinct from those of the homodimer or oligomer thus adding another level of complexity to how GPCRs are activated, signal and traffick in the cell. Dimerization may also play a role in influencing the activity of agonists and antagonists. We are only beginning to unravel how and why such complexes are formed, the functional implications of which will have an enormous impact on GPCR biology. Future research that studies GPCRs as dimeric or oligomeric complexes will enhance not only our understanding of GPCRs in cellular function but will also be critical for novel drug design and improved treatment of the vast array of GPCR-related conditions.

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Year:  2003        PMID: 14726257     DOI: 10.1016/j.yfrne.2003.10.002

Source DB:  PubMed          Journal:  Front Neuroendocrinol        ISSN: 0091-3022            Impact factor:   8.606


  23 in total

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8.  CRH-stimulation of cyclic adenosine 5'-monophosphate pathway is partially inhibited by the coexpression of CRH-R1 and CRH-R2alpha.

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9.  Rescue of defective G protein-coupled receptor function in vivo by intermolecular cooperation.

Authors:  Adolfo Rivero-Müller; Yen-Yin Chou; Inhae Ji; Svetlana Lajic; Aylin C Hanyaloglu; Kim Jonas; Nafis Rahman; Tae H Ji; Ilpo Huhtaniemi
Journal:  Proc Natl Acad Sci U S A       Date:  2010-01-11       Impact factor: 11.205

10.  Illuminating the life of GPCRs.

Authors:  Ilka Böhme; Annette G Beck-Sickinger
Journal:  Cell Commun Signal       Date:  2009-07-14       Impact factor: 5.712

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