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PMID: 8288567 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Expression, purification, and characterization of the G protein-coupled receptor kinase GRK5.

The Journal of biological chemistry ·Vol. 269 ·No. 2 ·1994-01-14 ·Pages 1099-105

Kunapuli P, Onorato JJ, Hosey MM, Benovic JL

Abstract

G protein-coupled receptor kinases (GRKs) such as rhodopsin kinase and the beta-adrenergic receptor kinase (beta ARK) play an important role in agonist-specific phosphorylation and desensitization of G protein-coupled receptors. GRK5 is a recently identified member of the GRK family that has greater homology with rhodopsin kinase than with beta ARK. To further characterize the activity of GRK5, it has been overexpressed in Sf9 insect cells and purified by successive chromatography on S-Sepharose and Mono S columns. GRK5 phosphorylates the beta 2-adrenergic receptor (beta 2AR), m2 muscarinic cholinergic receptor, and rhodopsin in an agonist-dependent manner to maximal stoichiometries of approximately 2.5, 1.5, and 1 mol of phosphate/mol of receptor, respectively, with Km values of approximately 0.5 microM for the beta 2AR, approximately 16 microM for rhodopsin, and approximately 24 microM for ATP. Peptide phosphorylation studies suggest that in contrast to beta ARK and rhodopsin kinase, GRK5 preferentially phosphorylates on nonacidic peptides with a Km of approximately 1.5 mM. Heparin and dextran sulfate were found to be potent inhibitors of GRK5 with IC50 values of approximately 1 nM, thereby being at least 150-fold more potent on GRK5 than on beta ARK. GRK5 can also be activated by polycations, with 10 microM polylysine promoting an approximately 2.6-fold activation. Overall, these studies demonstrate that GRK5 has unique properties that distinguish it from other members of the GRK family and that likely play an important role in modulating its mechanism of action.

Related Genes
MeSH Terms
Amino Acid Sequence Cations, Divalent G-Protein-Coupled Receptor Kinase 5 GTP-Binding Proteins/metabolism Humans Kinetics Molecular Sequence Data Peptides/chemistry,metabolism Protein Kinases/metabolism Protein Serine-Threonine Kinases Receptor Protein-Tyrosine Kinases/metabolism Receptors, Cell Surface/metabolism Recombinant Proteins Substrate Specificity
Chemicals
Cations, Divalent Peptides Receptors, Cell Surface Recombinant Proteins Protein Kinases Receptor Protein-Tyrosine Kinases Protein Serine-Threonine Kinases G-Protein-Coupled Receptor Kinase 5 GRK5 protein, human GTP-Binding Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kunapuli P
Department of Pharmacology, Jefferson Cancer Institute, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.
Onorato J J
Hosey M M
Benovic J L
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1994-01-14
Pages
1099-105
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · GM44944 · United States
NHLBI NIH HHS · HL31601 · United States
NHLBI NIH HHS · HL45964 · United States
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