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Determination of bradykinin B2 receptor in vivo phosphorylation sites and their role in receptor function
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm, Ludwig Institute for Cancer Research.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm, Ludwig Institute for Cancer Research.
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2001 (English)In: Journal of Biological Chemistry, ISSN 0021-9258, E-ISSN 1083-351X, Vol. 276, no 44, 40431-40440 p.Article in journal (Refereed) Published
Abstract [en]

Reversible phosphorylation plays important roles in G protein-coupled receptor signaling, desensitization, and endocytosis, yet the precise location and role of in vivo phosphorylation sites is unknown for most receptors. Using metabolic 32P labeling and phosphopeptide sequencing we provide a complete phosphorylation map of the human bradykinin B2 receptor in its native cellular environment. We identified three serine residues, Ser(339), Ser(346), and Ser(348), at the C-terminal tail as principal phosphorylation sites. Constitutive phosphorylation occurs at Ser(348), while ligand-induced phosphorylation is found at Ser(339) and Ser(346)/Ser(348) that could be executed by several G protein-coupled receptor kinases. In addition, we found a protein kinase C-dependent phosphorylation of Ser(346) that was mutually exclusive with the basal phosphorylation at Ser(348) and therefore may be implicated in differential regulation of B2 receptor activation. Functional analysis of receptor mutants revealed that a low phosphorylation stoichiometry is sufficient to initiate receptor sequestration while a clustered phosphorylation around Ser(346) is necessary for desensitization of the B2 receptor-induced phospholipase C activation. This was further supported by the specifically reduced Ser(346)/Ser(348) phosphorylation observed upon stimulation with a nondesensitizing B2 receptor agonist. The differential usage of clustered phosphoacceptor sites points to distinct roles of multiple kinases in controlling G protein-coupled receptor function.

Place, publisher, year, edition, pages
2001. Vol. 276, no 44, 40431-40440 p.
Keyword [en]
Amino Acid Sequence, Cell Line, Humans, Kinetics, Molecular Sequence Data, Mutagenesis; Site-Directed, Peptide Mapping, Phosphorylation, Receptor; Bradykinin B2, Receptors; Bradykinin/chemistry/genetics/*metabolism/physiology, Research Support; Non-U.S. Gov't, Serine/*metabolism
National Category
Medical and Health Sciences
URN: urn:nbn:se:uu:diva-73600DOI: 10.1074/jbc.M107024200PubMedID: 11517230OAI: oai:DiVA.org:uu-73600DiVA: diva2:101510
Available from: 2005-06-10 Created: 2005-06-10 Last updated: 2013-10-30Bibliographically approved

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Publisher's full textPubMedhttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=11517230&dopt=Citation

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Wernstedt, Christer
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