Kinetic evaluation of the Na‐K pump reaction mechanism.
- 1 December 1977
- journal article
- research article
- Published by Wiley in The Journal of Physiology
- Vol. 273 (2) , 489-514
- https://doi.org/10.1113/jphysiol.1977.sp012106
Abstract
The ouabain-sensitive K influx was measured at varying external K concentrations ([K]o) and at several fixed internal Na concentrations ([Na]c). The cells [human blood cells] were nominally K-free and the solutions Na-free. Both the apparent maximal velocity (VM) and the apparent Michaelis constant for K (KK) increased as Nac increased. The ratio app. VM/app. KK increased with increasing Nac. The ouabain-sensitive Cs influx was measured at varying external Cs concentrations and at several fixed Nac in K-free cells and Na-free solutions. Both app. VM and app. KCs increased as Nac increased and the ratio app. VM/app. KCs increased with increasing Nac. The data were evaluated in terms of a ping-pong model and a simultaneous model for the pump reaction mechanism. The simultaneous model described the data adequately and the ping-pong models did not. The K influx was measured at varying external K concentrations in solutions containing Na and at a low and high Nac; the cells contained K. The relation between the pump rate and the external K concentration was sigmoid. A Hill equation was fitted to the data. KK was higher in the high Nac cells, but the Hill coefficient (n) was not altered as Nac increased. The K influx was measured at varying internal Na concentrations and 2 fixed external K concentrations; the cells contained K. The relation between the pump rate and Nac was sigmoid. When a Hill equation was fitted to the data, KNac was higher at the high external K concentration, but n was the same at both K concentrations.This publication has 42 references indexed in Scilit:
- Purification and characterization of (Na+, K+)-ATPase. V. Conformational changes in the enzyme. Transitions between the Na-form and the K-form studied with tryptic digestion as a toolBiochimica et Biophysica Acta (BBA) - Biomembranes, 1975
- The reaction mechanism of the sodium pumpBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1975
- EXPERIMENTAL AND THEORETICAL EXAMINATION OF THE FLIP‐FLOP MODEL OF (Na, K)‐ATPase FUNCTIONAnnals of the New York Academy of Sciences, 1974
- Affinity of the (Na+ + K+)‐dependent ATPase for Na+ measured by NA+‐modified enzyme inactivationFEBS Letters, 1974
- The uncoupled extruson of Na+ through the Na+ pumpBiochimica et Biophysica Acta (BBA) - Biomembranes, 1973
- Recoupling the Na-K PumpJournal of Clinical Investigation, 1972
- Active Sodium and Potassium Transport in High Potassium and Low Potassium Sheep Red CellsThe Journal of general physiology, 1971
- Molecular weight of Na, K-ATPase approximated by the radiation inactivation methodBiochemical and Biophysical Research Communications, 1967
- A kinetic method for investigating hypothetical models of the sodium pumpBiochimica et Biophysica Acta (BBA) - Biophysics including Photosynthesis, 1966
- The linkage of sodium, potassium, and ammonium active transport across the human erythrocyte membraneBiochimica et Biophysica Acta, 1957