. Studies on the relationship between structure and function in the Ca2+ pumping ATPase of plasma membranes will be continued. These Ca2+ pumps exist in the plasma membranes of heart, smooth muscle, kidney, brain, intestinal epithelium, erythrocyte and many other cell types. They are involved in control of intracellular Ca2+ levels in cells of all kinds, and in movement of Ca2+ across epithelial cell layers such as the intestinal and kidney tubule epithelium. Information about the regulation of these pumps may thus give information relevant to hypertension and kidney disease, among other conditions. The pump consists of a single polypeptide chain of molecular weight 127,000-137,000 (the exact molecular weight depends on the isoform). Four genes encode different isoforms, and additional forms are created by alternate splices. The applicant's laboratory has succeeded in expressing this pump on COS cells and have developed an assay system for determining the activity of the expressed enzyme. Studies are proposed to extend the present knowledge of the function of the different parts of this enzyme. The structure-function relationships will be mapped by site-directed mutagenesis (utilizing the COS cell system). The properties of the isoforms will be determined which will hep to define the role of the different forms. Antibodies will be developed to identify the isoforms expressed in different cell types.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM028835-21
Application #
6385399
Study Section
Physical Biochemistry Study Section (PB)
Program Officer
Chin, Jean
Project Start
1980-08-01
Project End
2002-08-31
Budget Start
2001-07-01
Budget End
2002-08-31
Support Year
21
Fiscal Year
2001
Total Cost
$265,602
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
City
Rochester
State
MN
Country
United States
Zip Code
55905
Strehler, Emanuel E (2013) Plasma membrane calcium ATPases as novel candidates for therapeutic agent development. J Pharm Pharm Sci 16:190-206
Caride, Ariel J; Bennett, Richard D; Strehler, Emanuel E (2010) Kinetic analysis reveals differences in the binding mechanism of calmodulin and calmodulin-like protein to the IQ motifs of myosin-10. Biochemistry 49:8105-16
Bajzer, Zeljko; Huzak, Miljenko; Neff, Kevin L et al. (2008) Mathematical analysis of models for reaction kinetics in intracellular environments. Math Biosci 215:35-47
Caride, Ariel J; Filoteo, Adelaida G; Penniston, John T et al. (2007) The plasma membrane Ca2+ pump isoform 4a differs from isoform 4b in the mechanism of calmodulin binding and activation kinetics: implications for Ca2+ signaling. J Biol Chem 282:25640-8
Ribiczey, Polett; Tordai, Attila; Andrikovics, Hajnalka et al. (2007) Isoform-specific up-regulation of plasma membrane Ca2+ATPase expression during colon and gastric cancer cell differentiation. Cell Calcium 42:590-605
Strehler, E E; Filoteo, A G; Penniston, J T et al. (2007) Plasma-membrane Ca(2+) pumps: structural diversity as the basis for functional versatility. Biochem Soc Trans 35:919-22
Vanagas, Laura; Rossi, Rolando C; Caride, Ariel J et al. (2007) Plasma membrane calcium pump activity is affected by the membrane protein concentration: evidence for the involvement of the actin cytoskeleton. Biochim Biophys Acta 1768:1641-9
Paszty, Katalin; Antalffy, Geza; Hegedus, Luca et al. (2007) Cleavage of the plasma membrane Ca+ATPase during apoptosis. Ann N Y Acad Sci 1099:440-50
Strehler, Emanuel E; Caride, Ariel J; Filoteo, Adelaida G et al. (2007) Plasma membrane Ca2+ ATPases as dynamic regulators of cellular calcium handling. Ann N Y Acad Sci 1099:226-36
Kip, Sertac N; Strehler, Emanuel E (2007) Rapid downregulation of NCX and PMCA in hippocampal neurons following H2O2 oxidative stress. Ann N Y Acad Sci 1099:436-9

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