Korzeniewski B
Institute of Molecular Biology, Jagiellonian University, al. Mickiewicza 3, 31-120 Krakow, Poland.
Biochem J. 1998 Mar 15;330 ( Pt 3)(Pt 3):1189-95. doi: 10.1042/bj3301189.
The dynamic computer model of oxidative phosphorylation developed previously and successfully tested for large-scale changes in fluxes and metabolite concentrations was used to study the question of how the rate of ATP production by oxidative phosphorylation is adjusted to meet the energy demand during muscle contraction, which causes a great increase in ATP consumption in relation to the resting state. The changes in the respiration rate and ATP/ADP ratio after the onset of maximal work measured experimentally were compared with simulated changes in the respiration rate and ATP/ADP in several different cases, assuming direct activation of different steps by an external effector. On the basis of the computer simulations performed, it was possible to conclude which enzymes/metabolic blocks should be directly activated to cause the experimentally observable changes in fluxes and metabolite concentrations. The theoretical results obtained suggest that the parallel direct activation of actinomyosin-ATP-ase and oxidative phosphorylation by an external effector (for example calcium ions) is the main mechanism responsible for fitting of ATP production to ATP consumption, while the negative feedback via an increase in ADP concentration (decrease in ATP/ADP), which indirectly activates the ATP supply, plays only a minor role. Additionally, the conclusion is drawn that most of the oxidative phosphorylation steps should be directly activated in order to explain the observed changes in the respiration rate and ATP/ADP ratio (and also in other parameters) during muscle contraction. It is suggested that there should exist a universal external activator/regulatory mechanism which causes a parallel stimulation of different enzymes/processes. A possible nature of such an activator is shortly discussed.
先前开发并成功测试了用于通量和代谢物浓度大规模变化的氧化磷酸化动态计算机模型,用于研究在肌肉收缩期间氧化磷酸化产生ATP的速率如何调节以满足能量需求的问题,肌肉收缩会导致ATP消耗相对于静息状态大幅增加。将实验测量的最大运动开始后呼吸速率和ATP/ADP比值的变化与几种不同情况下呼吸速率和ATP/ADP的模拟变化进行比较,假设外部效应器直接激活不同步骤。基于所进行的计算机模拟,可以得出应该直接激活哪些酶/代谢途径以引起通量和代谢物浓度的实验可观察变化。获得的理论结果表明,外部效应器(例如钙离子)对肌动球蛋白-ATP酶和氧化磷酸化的平行直接激活是使ATP产生与ATP消耗相匹配的主要机制,而通过ADP浓度增加(ATP/ADP降低)的负反馈间接激活ATP供应仅起次要作用。此外,得出的结论是,为了解释肌肉收缩期间观察到的呼吸速率和ATP/ADP比值(以及其他参数)的变化,氧化磷酸化的大多数步骤应该被直接激活。有人认为应该存在一种通用的外部激活剂/调节机制,它能同时刺激不同的酶/过程。简要讨论了这种激活剂可能的性质。