This project aims to discover basic features of the mechanism and structure of the Na/K pump of animal cell membranes using (Na, K)ATPase purified from mammalian kidney. Phospholipid vesicles reconstituted with the purified (Na, K)ATPase are to be used for a study of Na and K fluxes, protein conformational changes monitored with fluorescence probes, and of functional site labelling and selective proteolytic digestion. Following our recent discovery of slow passive Na/K-pump mediated fluxes of Rb(K) in the vesicles, we intend now to investigate conditions which may affect these """"""""leak"""""""" fluxes and alter their rates relative to normal active K pumping. These conditions include transmembrane potentials and temperature, and the concentrations of protons, and K congeners.
The aim i s to enquire into the possibility of a varying efficiency of active K transport and to define in detail the roles of K occlusion and K/ligand binding interactions on E1 and E2 forms of the protein, in regulating optimal rates and efficiency of active K transport. Na fluxes in the vesicles will be characterized kinetically with the purpose of both testing predictions of the conventional transport models, and especially the possibility of variable Na/ATP coupling ratios and efficiency of active Na transport. In another application of the vesicles we shall attempt to identify and to label covalently carboxyl residues involved in cation binding and transport, and locate those residues along the a-chain utilizing selective proteolytic digestion. This should permit a distinction to be made between different transport models. The Na/K pump generates the normal trans-membrane Na and K gradients and is responsible for volume control, electrical and secretory activities etc. The significance of an understanding of the working and structure of the pump at the molecular level derives ultimately from its essential physiological roles, and a growing recognition that abnormalities in active transport may be involved in the aetiology of diseases such as essential hypertension.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM032286-06
Application #
3280980
Study Section
Physiology Study Section (PHY)
Project Start
1987-09-01
Project End
1990-08-31
Budget Start
1989-09-01
Budget End
1990-08-31
Support Year
6
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Weizmann Institute of Science
Department
Type
DUNS #
City
Rehovot
State
Country
Israel
Zip Code
76100
Shainskaya, A; Karlish, S J (1994) Evidence that the cation occlusion domain of Na/K-ATPase consists of a complex of membrane-spanning segments. Analysis of limit membrane-embedded tryptic fragments. J Biol Chem 269:10780-9
Or, E; David, P; Shainskaya, A et al. (1993) Effects of competitive sodium-like antagonists on Na,K-ATPase suggest that cation occlusion from the cytoplasmic surface occurs in two steps. J Biol Chem 268:16929-37
Karlish, S J; Goldshleger, R; Tal, D M et al. (1992) Identification of the cation binding domain of Na/K-ATPase. Acta Physiol Scand Suppl 607:69-76
Goldshleger, R; Tal, D M; Moorman, J et al. (1992) Chemical modification of Glu-953 of the alpha chain of Na+,K(+)-ATPase associated with inactivation of cation occlusion. Proc Natl Acad Sci U S A 89:6911-5
Karlish, S J; Goldshleger, R; Tal, D M et al. (1991) Structure of the cation binding sites of Na/K-ATPase. Soc Gen Physiol Ser 46:129-41
Goldshleger, R; Shahak, Y; Karlish, S J (1990) Electrogenic and electroneutral transport modes of renal Na/K ATPase reconstituted into proteoliposomes. J Membr Biol 113:139-54
Glynn, I M; Karlish, S J (1990) Occluded cations in active transport. Annu Rev Biochem 59:171-205
Steinberg, M; Karlish, S J (1989) Studies on conformational changes in Na,K-ATPase labeled with 5-iodoacetamidofluorescein. J Biol Chem 264:2726-34
Karlish, S J (1988) Measurement of active and passive Na+ and K+ fluxes in reconstituted vesicles. Methods Enzymol 156:179-88
Karlish, S J (1988) The mechanism of active cation transport by the Na/K-pump. Prog Clin Biol Res 273:207-16

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