Hill T L
Proc Natl Acad Sci U S A. 1979 Jan;76(1):232-5. doi: 10.1073/pnas.76.1.232.
We consider a small vesicle whose membrane transports a ligand L into the vesicle through enzymatic units of type A and transports L out of the vesicle through units of type B. Oxidative phosphorylation in mitochondria provides an example, in which L is H+. The kinetics of the two membrane systems (A and B) are coupled through the concentration of L in the vesicle. This interdependence causes the combined membrane system (A plus B) to simulate a single system whenever the net ligand transport into the vesicle is zero. For example, in oxidative phosphorylation, it was thought for some time that ATP was synthesized by the respiratory chain system (via an "active intermediate"). We give the simplest possible analyses of this kind of coupled system, which is very common, by using two-state enzymes for both A and B above. A numerical example is included that illustrates respiratory control in a qualitative way: although the respiratory chain flux by itself does not depend on ADP concentration, the steady-state flux of the coupled systems (respiratory chain and reverse ATPase) does depend on ADP concentration through the interior ligand (H+) concentration.
我们考虑一个小囊泡,其膜通过A型酶单位将配体L转运到囊泡内,并通过B型单位将L转运出囊泡。线粒体中的氧化磷酸化就是一个例子,其中L是H⁺。两个膜系统(A和B)的动力学通过囊泡内L的浓度相互耦合。这种相互依赖性使得每当进入囊泡的净配体转运为零时,组合膜系统(A加B)就模拟一个单一系统。例如,在氧化磷酸化中,有一段时间人们认为ATP是由呼吸链系统(通过“活性中间体”)合成的。我们通过对上述A和B都使用双态酶,对这种非常常见的耦合系统进行了尽可能简单的分析。文中包含一个数值示例,以定性方式说明了呼吸控制:尽管呼吸链通量本身不依赖于ADP浓度,但耦合系统(呼吸链和反向ATP酶)的稳态通量确实通过内部配体(H⁺)浓度依赖于ADP浓度。