The Na,K-ATPase is an important membrane-associated enzyme responsible for maintaining the high internal potassium concentration and low internal sodium concentration characteristic of most animal cells. The ion gradients created by the Na,K-ATPase are fundamental to such diverse cellular functions as the regulation of cell volume and pH, the uptake of nutrients and membrane excitability. The Na,K-ATPase belongs to a widely distributed class of P-type cation transporting proteins that includes the intracellular and plasma membrane Ca-ATPases, and the H,K-ATPase of gastric mucosa. All these P-type ATPases have similar structures and common reaction mechanisms. However, in addition to having different cation affinities these P-type ATPases can have different intracellular locations. Depending on the specific ATPase, these enzymes can be found at the plasma membrane or in cytoplasmic vesicles or organelles. The purpose of this project is to gain insight into the role of the individual Na,K- ATPase subunits in directing the assembly, cellular sorting and function of the enzyme. Using baculovirus-infected insect cells we have shown that the alpha-subunit has activity independent of the beta-subunit. This activity will be further characterized to determine if the unassociated alpha-subunit can mediate the occlusion and transport of ions. In addition, the properties of the naturally occurring truncated alpha isoform, alpha1T will be determined. To identify and characterize the regions responsible for the assembly and intracellular transport of the Na,K-ATPase, chimera alpha subunits consisting of the Na,K-, H,K- and Ca- ATPases will be constructed. These chimeric subunits will be used to characterize the intracellular transport of the P-type ATPases in insect and mammalian cells. To ascertain the domains important for the transport of ions and binding of inhibitors, the chimeric proteins will be characterized with respect to ion and inhibitor specificity. These studies should help in defining the role of the individual subunits and of specific domains of the subunits in the assembly, intracellular transport and function of the Na,K-ATPase.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM039746-06A1
Application #
2180001
Study Section
Physiology Study Section (PHY)
Project Start
1988-04-01
Project End
1998-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
6
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Washington University
Department
Physiology
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Kim, Mijeong; Habiba, Ayman; Doherty, Jason M et al. (2009) Regulation of mouse embryonic stem cell neural differentiation by retinoic acid. Dev Biol 328:456-71