Allosteric transitions and membrane-bound ATPase from rat tissues: The effect of fat deprivation on the allosteric inhibition by fluoride

In rats red a fat-sufficient diet, ATPases (ATP phosphohydrolase, EC 3.6.1.3) from heart, kidney and brain microsomes showed allosteric kinetics for the inhibition by F^?, with values ofn = ?2.0. In rats fed a far-free diet, the values ofn for the ATPases changed from ?2.0 to ?1.0 in heart and kidney microsomes. When these animals were then fed a fat-sufficient diet the values ofn reached the control values. In brain microsomal ATPases no modification of the values ofn were found between both groups of animals. The regulatory properties of the membrane on bound ATPases are discussed.