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Ca2+-myristoyl switch in the neuronal calcium sensor recoverin requires different functions of Ca2+-binding sites.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2002 Dec 27; Vol. 277 (52), pp. 50365-72. Date of Electronic Publication: 2002 Oct 21. - Publication Year :
- 2002
-
Abstract
- Recoverin is an EF-hand Ca(2+)-binding protein that is suggested to control the activity of the G-protein-coupled receptor kinase GRK-1 or rhodopsin kinase in a Ca(2+)-dependent manner. It undergoes a Ca(2+)-myristoyl switch when Ca(2+) binds to EF-hand 2 and 3. We investigated the mechanism of this switch by the use of point mutations in EF-hand 2 (E85Q) and 3 (E121Q) that impair their Ca(2+) binding. EF-hand 2 and 3 display different properties and serve different functions. Binding of Ca(2+) to recoverin is a sequential process, wherein EF-hand 3 is occupied first followed by the filling of EF-hand 2. After EF-hand 3 bound Ca(2+), the subsequent filling of EF-hand 2 triggers the exposition of the myristoyl group and in turn binding of recoverin to membranes. In addition, EF-hand 2 controls the mean residence time of recoverin at membranes by decreasing the dissociation rate of recoverin from membranes by 10-fold. We discuss this mechanism as one critical step for inhibition of rhodopsin kinase by recoverin.
- Subjects :
- Animals
Binding Sites
Biomarkers, Tumor metabolism
Calcium-Binding Proteins chemistry
Cattle
Cloning, Molecular
Electron Spin Resonance Spectroscopy
Escherichia coli genetics
Escherichia coli metabolism
G-Protein-Coupled Receptor Kinase 1
Hippocalcin
Kinetics
Liposomes
Mutagenesis, Site-Directed
Protein Kinases metabolism
Recombinant Proteins chemistry
Recombinant Proteins metabolism
Recoverin
Calcium metabolism
Calcium-Binding Proteins metabolism
Eye Proteins
Lipoproteins
Myristic Acid metabolism
Nerve Tissue Proteins
Rod Cell Outer Segment metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 277
- Issue :
- 52
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 12393897
- Full Text :
- https://doi.org/10.1074/jbc.M204338200