The human serotonin1A receptor exhibits G-protein-dependent cell surface dynamics
- PMID: 17123166
- DOI: 10.1007/s10719-006-9008-x
The human serotonin1A receptor exhibits G-protein-dependent cell surface dynamics
Abstract
Seven transmembrane domain G-protein-coupled receptors constitute the largest family of proteins in mammals. Signal transduction events mediated by such receptors are the primary means by which cells communicate with and respond to their external environment. The major paradigm in this signal transduction process is that stimulation of the receptor leads to the recruitment and activation of heterotrimeric GTP-binding proteins. These initial events, which are fundamental to all types of G-protein-coupled receptor signaling, occur at the plasma membrane via protein-protein interactions. As a result, the dynamics of the activated receptor on cell surfaces represents an important determinant in its encounter with G-proteins, and has significant impact on the overall efficiency of the signal transduction process. We have monitored the cell surface dynamics of the serotonin(1A) receptor, an important member of the G-protein-coupled receptor superfamily, in relation to its interaction with G-proteins. Fluorescence recovery after photobleaching experiments carried out with the receptor tagged to the enhanced yellow fluorescent protein indicate that G-protein activation alters the diffusion properties of the receptor in a manner suggesting the activation process leads to dissociation of G-proteins from the receptor. This result demonstrates that the cell surface dynamics of the serotonin(1A) receptor is modulated in a G-protein-dependent manner. Importantly, this result could provide the basis for a sensitive and powerful approach to assess receptor/G-protein interaction in an intact cellular environment.
Similar articles
-
G-protein-dependent cell surface dynamics of the human serotonin1A receptor tagged to yellow fluorescent protein.Biochemistry. 2004 Dec 21;43(50):15852-62. doi: 10.1021/bi0480887. Biochemistry. 2004. PMID: 15595840
-
Cholesterol depletion induces dynamic confinement of the G-protein coupled serotonin(1A) receptor in the plasma membrane of living cells.Biochim Biophys Acta. 2007 Mar;1768(3):655-68. doi: 10.1016/j.bbamem.2007.01.002. Epub 2007 Jan 12. Biochim Biophys Acta. 2007. PMID: 17292852
-
Membrane organization and dynamics of the serotonin1A receptor in live cells.J Neurochem. 2011 Mar;116(5):726-33. doi: 10.1111/j.1471-4159.2010.07037.x. Epub 2011 Jan 7. J Neurochem. 2011. PMID: 21214564 Review.
-
Oligomerization of the serotonin(1A) receptor in live cells: a time-resolved fluorescence anisotropy approach.J Phys Chem B. 2011 Oct 6;115(39):11439-47. doi: 10.1021/jp201458h. Epub 2011 Sep 13. J Phys Chem B. 2011. PMID: 21866959
-
Membrane organization and dynamics of the G-protein-coupled serotonin1A receptor monitored using fluorescence-based approaches.J Fluoresc. 2005 Sep;15(5):785-96. doi: 10.1007/s10895-005-2988-2. J Fluoresc. 2005. PMID: 16341798 Review.
Cited by
-
Disrupting microtubule network immobilizes amoeboid chemotactic receptor in the plasma membrane.Biochim Biophys Acta. 2011 Jun;1808(6):1701-8. doi: 10.1016/j.bbamem.2011.02.009. Epub 2011 Feb 18. Biochim Biophys Acta. 2011. PMID: 21334306 Free PMC article.
-
Thermodynamics of peptide and non-peptide interactions with the human 5HT1a receptor.Pharmacology. 2010;86(1):6-14. doi: 10.1159/000312684. Epub 2010 Jun 19. Pharmacology. 2010. PMID: 20559018 Free PMC article.
-
GFP fluorescence: A few lesser-known nuggets that make it work.J Biosci. 2018 Jul;43(3):421-430. J Biosci. 2018. PMID: 30002261
-
Is There a Role for GPCR Agonist Radiotracers in PET Neuroimaging?Front Mol Neurosci. 2019 Oct 18;12:255. doi: 10.3389/fnmol.2019.00255. eCollection 2019. Front Mol Neurosci. 2019. PMID: 31680859 Free PMC article. Review.
-
Dynamics of somatostatin type 2A receptor cargoes in living hippocampal neurons.J Neurosci. 2008 Apr 23;28(17):4336-49. doi: 10.1523/JNEUROSCI.4379-07.2008. J Neurosci. 2008. PMID: 18434512 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials