Biology:GRK5

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Short description: Protein-coding gene in the species Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example


G protein-coupled receptor kinase 5 is a member of the G protein-coupled receptor kinase subfamily of the Ser/Thr protein kinases, and is most highly similar to GRK4 and GRK6.[1][2][3] The protein phosphorylates the activated forms of G protein-coupled receptors to regulate their signaling.

Function

G protein-coupled receptor kinases phosphorylate activated G protein-coupled receptors, which promotes the binding of an arrestin protein to the receptor. Arrestin binding to phosphorylated, active receptor prevents receptor stimulation of heterotrimeric G protein transducer proteins, blocking their cellular signaling and resulting in receptor desensitization. Arrestin binding also directs receptors to specific cellular internalization pathways, removing the receptors from the cell surface and also preventing additional activation. Arrestin binding to phosphorylated, active receptor also enables receptor signaling through arrestin partner proteins. Thus the GRK/arrestin system serves as a complex signaling switch for G protein-coupled receptors.[4]

GRK5 and the closely related GRK6 phosphorylate receptors at sites that encourage arrestin-mediated signaling rather than arrestin-mediated receptor desensitization, internalization and trafficking (in contrast to GRK2 and GRK3, which have the opposite effect).[5][6] This difference is one basis for pharmacological biased agonism (also called functional selectivity), where a drug binding to a receptor may bias that receptor’s signaling toward a particular subset of the actions stimulated by that receptor.[7][8]

GRK5 is widely expressed throughout the body, but with notably high expression in the lung, heart and placenta, with widespread expression at lower levels.[9] In humans, a GRK5 sequence polymorphism at residue 41 (leucine rather than glutamine) that is most common in individuals with African ancestry leads to elevated GRK5-mediated desensitization of airway beta2-adrenergic receptors, a drug target in asthma.[10] In the mouse, GRK5 regulates the M2 subtype of Muscarinic acetylcholine receptors in airways and neurons, and mice lacking GRK5 have been proposed as a model for Alzheimer’s disease.[11][12][13] In zebrafish and in humans, loss of GRK5 function has been associated with heart defects due to heterotaxy, a series of developmental defects arising from improper left-right laterality during organogenesis.[14] Overexpression of GRK5 in the heart of mice has shown that GRK5 regulates beta2-adrenergic receptors, but GRK5 overexpression or deletion does not affect signaling by the angiotensin II AT1 receptor in the heart.[15][16]

References

  1. ↑ "Cloning and expression of GRK5: a member of the G protein-coupled receptor kinase family". Proceedings of the National Academy of Sciences 90 (12): 5588–92. Jun 1993. doi:10.1073/pnas.90.12.5588. PMID 7685906. Bibcode: 1993PNAS...90.5588K. 
  2. ↑ "Protein kinases that phosphorylate activated G protein-coupled receptors". The FASEB Journal 9 (2): 175–182. 1995. doi:10.1096/fasebj.9.2.7781920. PMID 7781920. 
  3. ↑ "Entrez Gene: GRK5 G protein-coupled receptor kinase 5". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2869. 
  4. ↑ "GPCR Signaling Regulation: The Role of GRKs and Arrestins". Frontiers in Pharmacology 10: 125. 2019. doi:10.3389/fphar.2019.00125. PMID 30837883. 
  5. ↑ "Functional antagonism of different G protein-coupled receptor kinases for beta-arrestin-mediated angiotensin II receptor signaling". Proceedings of the National Academy of Sciences 102 (5): 1442–1447. 2005. doi:10.1073/pnas.0409532102. PMID 15671181. Bibcode: 2005PNAS..102.1442K. 
  6. ↑ "Different G protein-coupled receptor kinases govern G protein and beta-arrestin-mediated signaling of V2 vasopressin receptor". Proceedings of the National Academy of Sciences 102 (5): 1448–1453. 2005. doi:10.1073/pnas.0409534102. PMID 15671180. Bibcode: 2005PNAS..102.1448R. 
  7. ↑ "Selective engagement of G protein coupled receptor kinases (GRKs) encodes distinct functions of biased ligands". Proceedings of the National Academy of Sciences 106 (24): 9649–9654. 2009. doi:10.1073/pnas.0904361106. PMID 19497875. Bibcode: 2009PNAS..106.9649Z. 
  8. ↑ "G protein-coupled receptor kinases (GRKs) orchestrate biased agonism at the β2-adrenergic receptor". Science Signaling 11 (544): eaar7084. 2018. doi:10.1126/scisignal.aar7084. PMID 30131371. 
  9. ↑ "Cloning and expression of GRK5: a member of the G protein-coupled receptor kinase family". Proceedings of the National Academy of Sciences 90 (12): 5588–5592. 1993. doi:10.1073/pnas.90.12.5588. PMID 7685906. Bibcode: 1993PNAS...90.5588K. 
  10. ↑ "A polymorphism of G-protein coupled receptor kinase5 alters agonist-promoted desensitization of beta2-adrenergic receptors". Pharmacogenetics and Genomics 18 (8): 729–732. 2008. doi:10.1097/FPC.0b013e32830967e9. PMID 18622265. 
  11. ↑ "Muscarinic supersensitivity and impaired receptor desensitization in G protein-coupled receptor kinase 5-deficient mice". Neuron 24 (4): 1029–1036. 1999. doi:10.1016/S0896-6273(00)81048-X. PMID 10624964. 
  12. ↑ "G protein-coupled receptor kinase 5 regulates airway responses induced by muscarinic receptor activation". American Journal of Physiology. Lung Cellular and Molecular Physiology 286 (2): L312–L319. 2004. doi:10.1152/ajplung.00255.2003. PMID 14565944. 
  13. ↑ "GRK5 Deficiency Leads to Selective Basal Forebrain Cholinergic Neuronal Vulnerability". Scientific Reports 6: 26116. 2016. doi:10.1038/srep26116. PMID 27193825. Bibcode: 2016NatSR...626116H. 
  14. ↑ "The analysis of heterotaxy patients reveals new loss-of-function variants of GRK5". Scientific Reports 6: 33231. 2016. doi:10.1038/srep33231. PMID 27618959. Bibcode: 2016NatSR...633231L. 
  15. ↑ "Receptor-specific in vivo desensitization by the G protein-coupled receptor kinase-5 in transgenic mice". Proceedings of the National Academy of Sciences 93 (18): 9954–9959. 1996. doi:10.1073/pnas.93.18.9954. PMID 8790438. Bibcode: 1996PNAS...93.9954R. 
  16. ↑ "Beta-arrestin2-mediated inotropic effects of the angiotensin II type 1A receptor in isolated cardiac myocytes". Proceedings of the National Academy of Sciences 103 (44): 16284–16289. 2006. doi:10.1073/pnas.0607583103. PMID 17060617. Bibcode: 2006PNAS..10316284R. 

Further reading




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