Rigoulet M, Leverve X, Fontaine E, Ouhabi R, Guérin B
Institut de Biochimie et de Génétique Cellulaires du CNRS, Université Bordeaux II, France.
Mol Cell Biochem. 1998 Jul;184(1-2):35-52.
The purpose of this work was to show how the quantitative definition of the different parameters involved in mitochondrial oxidative phosphorylation makes it possible to characterize the mechanisms by which the yield of ATP synthesis is affected. Three different factors have to be considered: (i) the size of the different forces involved (free energy of redox reactions and ATP synthesis, proton electrochemical difference); (ii) the physical properties of the inner mitochondrial membrane in terms of leaks (H+ and cations); and finally (iii) the properties of the different proton pumps involved in this system (kinetic properties, regulation, modification of intrinsic stoichiometry). The data presented different situations where one or more of these parameters are affected, leading to a different yield of oxidative phosphorylation. (1) By manipulating the actual flux through each of the respiratory chain units at constant protonmotive force in yeast mitochondria, we show that the ATP/O ratio decreases when the flux increases. Moreover, the highest efficiency was obtained when the respiratory rate was low and almost entirely controlled by the electron supply. (2) By using almitrine in different kinds of mitochondria, we show that this drug leads to a decrease in ATP synthesis efficiency by increasing the H+/ATP stoichiometry ofATP synthase (Rigoulet M et al. Biochim Biophys Acta 1018: 91-97, 1990). Since this enzyme is reversible, it was possible to test the effect of this drug on the reverse reaction of the enzyme i.e. extrusion of protons catalyzed by ATP hydrolysis. Hence, we are able to prove that, in this case, the decrease in efficiency of oxidative phosphorylation is due to a change in the mechanistic stoichiometry of this proton pump. To our knowledge, this is the first example of a modification in oxidative phosphorylation yield by a change in mechanistic stoichiometry of one of the proton pumps involved. (3) In a model of polyunsaturated fatty acid deficiency in rat, it was found that non-ohmic proton leak was increased, while ohmic leak was unchanged. Moreover, an increase in redox slipping was also involved, leading to a complex picture. However, the respective role of these two mechanisms may be deduced from their intrinsic properties. For each steady state condition, the quantitative effect of these two mechanisms in the decrease of oxidative phosphorylation efficiency depends on the values of different fluxes or forces involved. (4) Finally the comparison of the thermokinetic data in view of the three dimensional-structure of some pumps (X-ray diffraction) also gives some information concerning the putative mechanism of coupling (i.e. redox loop or proton pump) and their kinetic control versus regulation of mitochondrial oxidative phosphorylation.
这项工作的目的是展示线粒体氧化磷酸化过程中涉及的不同参数的定量定义如何使表征ATP合成产量受影响的机制成为可能。必须考虑三个不同因素:(i)所涉及的不同力的大小(氧化还原反应和ATP合成的自由能、质子电化学差);(ii)线粒体内膜在泄漏方面(H⁺和阳离子)的物理性质;最后(iii)该系统中涉及的不同质子泵的性质(动力学性质、调节、内在化学计量的改变)。所呈现的数据展示了这些参数中的一个或多个受到影响的不同情况,从而导致氧化磷酸化的产量不同。(1)通过在酵母线粒体中恒定质子动力势的情况下操纵通过每个呼吸链单元的实际通量,我们表明当通量增加时,ATP/O比值降低。此外,当呼吸速率较低且几乎完全由电子供应控制时,可获得最高效率。(2)通过在不同类型的线粒体中使用氨苯蝶啶,我们表明这种药物通过增加ATP合酶的H⁺/ATP化学计量导致ATP合成效率降低(里古莱 M等人。生物化学与生物物理学报1018:91 - 97,1990)。由于这种酶是可逆的,有可能测试这种药物对该酶的逆反应的影响,即由ATP水解催化的质子外排。因此,我们能够证明,在这种情况下,氧化磷酸化效率的降低是由于该质子泵的机制化学计量的变化。据我们所知,这是通过改变所涉及的一个质子泵的机制化学计量来改变氧化磷酸化产量的第一个例子。(3)在大鼠多不饱和脂肪酸缺乏的模型中,发现非欧姆质子泄漏增加,而欧姆泄漏不变。此外,还涉及氧化还原滑移的增加,导致情况复杂。然而,这两种机制各自的作用可以从它们的内在性质推导出来。对于每种稳态条件,这两种机制在氧化磷酸化效率降低方面的定量影响取决于所涉及的不同通量或力的值。(4)最后,鉴于一些泵的三维结构(X射线衍射)对热动力学数据进行比较,也给出了一些关于耦合的假定机制(即氧化还原环或质子泵)及其对线粒体氧化磷酸化的动力学控制与调节的信息。