The objective is to understand the enzymology and regulation of the phosphoprotein phosphatases involved in the activation of glycogen synthase in skeletal muscle. Bifunctional protein cross-linking reagents and immunoprecipitation techniques would be used to establish the subunit structure of the glycogen-bound high molecular weight phosphatase. The relationships between the glycogen-bound and soluble type 1 phosphatases would be investigated by using protein chemistry techniques. Synthetic phosphopeptides would be prepared to determine the minimal structural determinants for the action of phosphatases. The specificity of the native phosphatases towards various sites of glycogen synthase and possible role of site site interaction in the regulation of synthase phosphatase activity would be investigated. Glycogen synthase preparations containing 32P-phosphate in different sites would be prepared to investigate the role of site specific phosphatases in the activation of glycogen synthase in crude muscle extracts of normal and diabetic rabbits. Possible role of heat stable protein inhibitors and the regulatory subunit of cAMP-dependent protein kinase in the regulation of phosphatases would be investigated. The proposed investigation would advance our knowledge into the structure and regulation of phosphatases and would help understand the mechanism of slow activation of glycogen synthase in tissues of diabetic animals. The long term aim of the project is to understand the mechanism of activation of glycogen synthase by insulin.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
7R01DK026334-08
Application #
3227835
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1987-09-01
Project End
1989-08-31
Budget Start
1987-09-01
Budget End
1988-08-31
Support Year
8
Fiscal Year
1987
Total Cost
Indirect Cost
Name
California State University Long Beach
Department
Type
Schools of Arts and Sciences
DUNS #
City
Long Beach
State
CA
Country
United States
Zip Code
90840
Honkanen, R E; Zwiller, J; Daily, S L et al. (1991) Identification, purification, and characterization of a novel serine/threonine protein phosphatase from bovine brain. J Biol Chem 266:6614-9
Khatra, B S; Nguyen, O; Tuazon, P T et al. (1991) A ribosomal protein S6 kinase copurifies with phosphatase-1 activating factor. Arch Biochem Biophys 284:186-92
Honkanen, R E; Dukelow, M; Zwiller, J et al. (1991) Cyanobacterial nodularin is a potent inhibitor of type 1 and type 2A protein phosphatases. Mol Pharmacol 40:577-83
Guan, R J; Khatra, B S; Cohlberg, J A (1991) Phosphorylation of bovine neurofilament proteins by protein kinase FA (glycogen synthase kinase 3). J Biol Chem 266:8262-7
Honkanen, R E; Zwiller, J; Moore, R E et al. (1990) Characterization of microcystin-LR, a potent inhibitor of type 1 and type 2A protein phosphatases. J Biol Chem 265:19401-4