Beer Samantha M, Taylor Ellen R, Brown Stephanie E, Dahm Christina C, Costa Nikola J, Runswick Michael J, Murphy Michael P
Medical Research Council Dunn Human Nutrition Unit, Wellcome Trust-MRC Building, Hills Road, Cambridge CB2 2XY, United Kingdom.
J Biol Chem. 2004 Nov 12;279(46):47939-51. doi: 10.1074/jbc.M408011200. Epub 2004 Aug 30.
The redox poise of the mitochondrial glutathione pool is central in the response of mitochondria to oxidative damage and redox signaling, but the mechanisms are uncertain. One possibility is that the oxidation of glutathione (GSH) to glutathione disulfide (GSSG) and the consequent change in the GSH/GSSG ratio causes protein thiols to change their redox state, enabling protein function to respond reversibly to redox signals and oxidative damage. However, little is known about the interplay between the mitochondrial glutathione pool and protein thiols. Therefore we investigated how physiological GSH/GSSG ratios affected the redox state of mitochondrial membrane protein thiols. Exposure to oxidized GSH/GSSG ratios led to the reversible oxidation of reactive protein thiols by thiol-disulfide exchange, the extent of which was dependent on the GSH/GSSG ratio. There was an initial rapid phase of protein thiol oxidation, followed by gradual oxidation over 30 min. A large number of mitochondrial proteins contain reactive thiols and most of these formed intraprotein disulfides upon oxidation by GSSG; however, a small number formed persistent mixed disulfides with glutathione. Both protein disulfide formation and glutathionylation were catalyzed by the mitochondrial thiol transferase glutaredoxin 2 (Grx2), as were protein deglutathionylation and the reduction of protein disulfides by GSH. Complex I was the most prominent protein that was persistently glutathionylated by GSSG in the presence of Grx2. Maintenance of complex I with an oxidized GSH/GSSG ratio led to a dramatic loss of activity, suggesting that oxidation of the mitochondrial glutathione pool may contribute to the selective complex I inactivation seen in Parkinson's disease. Most significantly, Grx2 catalyzed reversible protein glutathionylation/deglutathionylation over a wide range of GSH/GSSG ratios, from the reduced levels accessible under redox signaling to oxidized ratios only found under severe oxidative stress. Our findings indicate that Grx2 plays a central role in the response of mitochondria to both redox signals and oxidative stress by facilitating the interplay between the mitochondrial glutathione pool and protein thiols.
线粒体谷胱甘肽池的氧化还原平衡在其对氧化损伤和氧化还原信号的反应中起着核心作用,但其机制尚不清楚。一种可能性是谷胱甘肽(GSH)氧化为谷胱甘肽二硫化物(GSSG)以及随之而来的GSH/GSSG比值变化会导致蛋白质硫醇改变其氧化还原状态,使蛋白质功能能够对氧化还原信号和氧化损伤做出可逆反应。然而,关于线粒体谷胱甘肽池与蛋白质硫醇之间的相互作用知之甚少。因此,我们研究了生理GSH/GSSG比值如何影响线粒体膜蛋白硫醇的氧化还原状态。暴露于氧化型GSH/GSSG比值会导致反应性蛋白硫醇通过硫醇-二硫化物交换发生可逆氧化,其程度取决于GSH/GSSG比值。蛋白硫醇氧化最初有一个快速阶段,随后在接下来的30分钟内逐渐氧化。大量线粒体蛋白含有反应性硫醇,其中大多数在被GSSG氧化后形成蛋白内二硫键;然而,少数会与谷胱甘肽形成持久的混合二硫键。蛋白二硫键的形成和谷胱甘肽化均由线粒体硫醇转移酶谷氧还蛋白2(Grx2)催化,蛋白去谷胱甘肽化以及GSH对蛋白二硫键的还原也是如此。在存在Grx2的情况下,复合体I是最显著的被GSSG持续谷胱甘肽化的蛋白。维持复合体I处于氧化型GSH/GSSG比值会导致其活性急剧丧失,这表明线粒体谷胱甘肽池的氧化可能导致帕金森病中所见的复合体I选择性失活。最重要的是,Grx2在很宽的GSH/GSSG比值范围内催化可逆的蛋白谷胱甘肽化/去谷胱甘肽化,从氧化还原信号作用下可达到的还原水平到仅在严重氧化应激下才会出现的氧化比值。我们的研究结果表明,Grx2通过促进线粒体谷胱甘肽池与蛋白硫醇之间的相互作用,在线粒体对氧化还原信号和氧化应激的反应中发挥核心作用。