Yanamala Naveena, Kapralov Alexander A, Djukic Mirjana, Peterson Jim, Mao Gaowei, Klein-Seetharaman Judith, Stoyanovsky Detcho A, Stursa Jan, Neuzil Jiri, Kagan Valerian E
From the Center for Free Radical and Antioxidant Health, the Departments of Environmental and Occupational Health.
the Departments of Environmental and Occupational Health.
J Biol Chem. 2014 Nov 21;289(47):32488-98. doi: 10.1074/jbc.M114.601377. Epub 2014 Oct 2.
Cytochrome c is a multifunctional hemoprotein in the mitochondrial intermembrane space whereby its participation in electron shuttling between respiratory complexes III and IV is alternative to its role in apoptosis as a peroxidase activated by interaction with cardiolipin (CL), and resulting in selective CL peroxidation. The switch from electron transfer to peroxidase function requires partial unfolding of the protein upon binding of CL, whose specific features combine negative charges of the two phosphate groups with four hydrophobic fatty acid residues. Assuming that other endogenous small molecule ligands with a hydrophobic chain and a negatively charged functionality may activate cytochrome c into a peroxidase, we investigated two hydrophobic anionic analogues of vitamin E, α-tocopherol succinate (α-TOS) and α-tocopherol phosphate (α-TOP), as potential inducers of peroxidase activity of cytochrome c. NMR studies and computational modeling indicate that they interact with cytochrome c at similar sites previously proposed for CL. Absorption spectroscopy showed that both analogues effectively disrupt the Fe-S(Met(80)) bond associated with unfolding of cytochrome c. We found that α-TOS and α-TOP stimulate peroxidase activity of cytochrome c. Enhanced peroxidase activity was also observed in isolated rat liver mitochondria incubated with α-TOS and tBOOH. A mitochondria-targeted derivative of TOS, triphenylphosphonium-TOS (mito-VES), was more efficient in inducing H2O2-dependent apoptosis in mouse embryonic cytochrome c(+/+) cells than in cytochrome c(-/-) cells. Essential for execution of the apoptotic program peroxidase activation of cytochrome c by α-TOS may contribute to its known anti-cancer pharmacological activity.
细胞色素c是一种存在于线粒体内膜间隙的多功能血红素蛋白,它参与呼吸复合物III和IV之间的电子穿梭,这与其作为过氧化物酶在细胞凋亡中的作用不同,后者通过与心磷脂(CL)相互作用而被激活,导致CL选择性过氧化。从电子传递功能转换为过氧化物酶功能需要在CL结合时蛋白质部分展开,CL的特定特征是两个磷酸基团的负电荷与四个疏水脂肪酸残基相结合。假设其他具有疏水链和带负电荷官能团的内源性小分子配体可能将细胞色素c激活为过氧化物酶,我们研究了维生素E的两种疏水阴离子类似物,α-生育酚琥珀酸酯(α-TOS)和α-生育酚磷酸酯(α-TOP),作为细胞色素c过氧化物酶活性的潜在诱导剂。核磁共振研究和计算模型表明,它们与细胞色素c在先前提出的与CL结合的类似位点相互作用。吸收光谱显示,这两种类似物均能有效破坏与细胞色素c展开相关的Fe-S(Met(80))键。我们发现α-TOS和α-TOP能刺激细胞色素c的过氧化物酶活性。在用α-TOS和叔丁基过氧化氢(tBOOH)孵育的分离大鼠肝线粒体中也观察到过氧化物酶活性增强。TOS的线粒体靶向衍生物三苯基鏻-TOS(mito-VES)在诱导小鼠胚胎细胞色素c(+/+)细胞中依赖H2O2的凋亡方面比在细胞色素c(-/-)细胞中更有效。α-TOS对细胞色素c进行过氧化物酶激活对于执行凋亡程序至关重要,这可能有助于其已知的抗癌药理活性。