The proposed work will be on the structure and function of the Mg2+-ATPase located in the transverse tubular membrane system of mammalian skeletal muscle. The physiological function of this protein is unknown, but it is clearly structurally unrelated to the well characterized cation transporting ATPases also present in skeletal muscle. The long term goals are to better understand the role of the transverse tubules in excitation/contraction coupling and to understand the general principles underlying the structural basis for function among the class of proteins known as ATPases. The immediate goals are the elucidation of the structure and function of the transverse tubule Mg2+-ATPase. The work on the Mg2+-ATPase will, involve the identification, purification, and affinity labelling of the protein(s) involved, as well as the elucidation of possible physiological functions. Polyclonal antibodies will be raised to immunolocalize the Mg2+-ATPase. N-terminal as well as internal protein sequence will be obtained on all putative sub-units, and the entire amino acid sequence will be deduced from the cDNA sequence. Models of the structure of the Mg2+-ATPase will be proposed and the structure compared to other possibly related proteins. This work will generate important information about a component of the transverse tubule membrane system, the Mg2+-ATPase, and its relationship to the process of excitation/contraction coupling, a very important yet poorly understood physiological process.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Modified Research Career Development Award (K04)
Project #
5K04AR001841-05
Application #
2077310
Study Section
Physiology Study Section (PHY)
Project Start
1991-07-01
Project End
1996-06-30
Budget Start
1995-07-01
Budget End
1996-06-30
Support Year
5
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Cincinnati
Department
Pharmacology
Type
Schools of Medicine
DUNS #
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Smith Jr, T M; Kirley, T L; Hennessey, T M (1997) A soluble ecto-ATPase from Tetrahymena thermophila: purification and similarity to the membrane-bound ecto-ATPase of smooth muscle. Arch Biochem Biophys 337:351-9
Dombrowski, K E; Brewer, K A; Maleckar, J R et al. (1997) Identification and partial characterization of ectoATPase expressed by immortalized B lymphocytes. Arch Biochem Biophys 340:10-8
Kirley, T L (1997) Complementary DNA cloning and sequencing of the chicken muscle ecto-ATPase. Homology with the lymphoid cell activation antigen CD39. J Biol Chem 272:1076-81
Stout, J G; Kirley, T L (1996) Control of cell membrane ecto-ATPase by oligomerization state: intermolecular cross-linking modulates ATPase activity. Biochemistry 35:8289-98
Stout, J G; Strobel, R S; Kirley, T L (1995) Properties of and proteins associated with the extracellular ATPase of chicken gizzard smooth muscle. A monoclonal antibody study. J Biol Chem 270:11845-50
Stout, J G; Strobel, R S; Kirley, T L (1995) Identification and immunolocalization of ecto-ATPDase in chicken stomach. Biochem Mol Biol Int 36:529-35
Stout, J G; Kirley, T L (1995) Inhibition of purified chicken gizzard smooth muscle ecto-ATPAse by P2 purinoceptor antagonists. Biochem Mol Biol Int 36:927-34
Stout, J G; Kirley, T L (1994) Tissue distribution of ecto-Mg-ATPase in adult and embryonic chicken. Biochem Mol Biol Int 32:745-53
Stout, J G; Kirley, T L (1994) Purification and characterization of the ecto-Mg-ATPase of chicken gizzard smooth muscle. J Biochem Biophys Methods 29:61-75
Stout, J G; Brittsan, A; Kirley, T L (1994) Brain ECTO-Mg-ATPase is not the neural cell adhesion molecule. Biochem Mol Biol Int 33:1091-8

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