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1
Oxygen sensitivity of mitochondrial reactive oxygen species generation depends on metabolic conditions.线粒体活性氧生成的氧敏感性取决于代谢条件。
J Biol Chem. 2009 Jun 12;284(24):16236-16245. doi: 10.1074/jbc.M809512200. Epub 2009 Apr 14.
2
Mitochondrial respiratory complex I: structure, function and implication in human diseases.线粒体呼吸链复合体I:结构、功能及在人类疾病中的意义
Curr Med Chem. 2009;16(10):1266-77. doi: 10.2174/092986709787846578.
3
Reactive oxygen species regulation by AIF- and complex I-depleted brain mitochondria.AIF和复合体I缺失的脑线粒体对活性氧的调节
Free Radic Biol Med. 2009 Apr 1;46(7):939-47. doi: 10.1016/j.freeradbiomed.2009.01.010.
4
The overexpression of major antioxidant enzymes does not extend the lifespan of mice.主要抗氧化酶的过度表达并不会延长小鼠的寿命。
Aging Cell. 2009 Feb;8(1):73-5. doi: 10.1111/j.1474-9726.2008.00449.x. Epub 2008 Dec 11.
5
How mitochondria produce reactive oxygen species.线粒体如何产生活性氧物种。
Biochem J. 2009 Jan 1;417(1):1-13. doi: 10.1042/BJ20081386.
6
The production of reactive oxygen species by complex I.复合体I产生活性氧物种。
Biochem Soc Trans. 2008 Oct;36(Pt 5):976-80. doi: 10.1042/BST0360976.
7
The mechanism of mitochondrial superoxide production by the cytochrome bc1 complex.细胞色素bc1复合物产生线粒体超氧化物的机制。
J Biol Chem. 2008 Aug 1;283(31):21649-54. doi: 10.1074/jbc.M803236200. Epub 2008 Jun 3.
8
Dissociation of superoxide production by mitochondrial complex I from NAD(P)H redox state.线粒体复合体I产生超氧化物与NAD(P)H氧化还原状态的解离。
FEBS Lett. 2008 May 28;582(12):1711-4. doi: 10.1016/j.febslet.2008.04.030. Epub 2008 Apr 28.
9
Diphenyleneiodonium acutely inhibits reactive oxygen species production by mitochondrial complex I during reverse, but not forward electron transport.二亚苯基碘鎓在逆向电子传递而非正向电子传递过程中,可急性抑制线粒体复合体I产生活性氧。
Biochim Biophys Acta. 2008 May;1777(5):397-403. doi: 10.1016/j.bbabio.2008.03.005. Epub 2008 Mar 18.
10
Structure of glycerol-3-phosphate dehydrogenase, an essential monotopic membrane enzyme involved in respiration and metabolism.甘油-3-磷酸脱氢酶的结构,一种参与呼吸和代谢的必需单拓扑膜酶。
Proc Natl Acad Sci U S A. 2008 Mar 4;105(9):3280-5. doi: 10.1073/pnas.0712331105. Epub 2008 Feb 22.

线粒体超氧产生的位置和拓扑结构。

The sites and topology of mitochondrial superoxide production.

机构信息

Buck Institute for Age Research, 8001 Redwood Blvd., Novato, CA 94945, USA.

出版信息

Exp Gerontol. 2010 Aug;45(7-8):466-72. doi: 10.1016/j.exger.2010.01.003. Epub 2010 Jan 11.

DOI:10.1016/j.exger.2010.01.003
PMID:20064600
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2879443/
Abstract

Mitochondrial superoxide production is an important source of reactive oxygen species in cells, and may cause or contribute to ageing and the diseases of ageing. Seven major sites of superoxide production in mammalian mitochondria are known and widely accepted. In descending order of maximum capacity they are the ubiquinone-binding sites in complex I (site IQ) and complex III (site IIIQo), glycerol 3-phosphate dehydrogenase, the flavin in complex I (site IF), the electron transferring flavoprotein:Q oxidoreductase (ETFQOR) of fatty acid beta-oxidation, and pyruvate and 2-oxoglutarate dehydrogenases. None of these sites is fully characterized and for some we only have sketchy information. The topology of the sites is important because it determines whether or not a site will produce superoxide in the mitochondrial matrix and be able to damage mitochondrial DNA. All sites produce superoxide in the matrix; site IIIQo and glycerol 3-phosphate dehydrogenase also produce superoxide to the intermembrane space. The relative contribution of each site to mitochondrial reactive oxygen species generation in the absence of electron transport inhibitors is unknown in isolated mitochondria, in cells or in vivo, and may vary considerably with species, tissue, substrate, energy demand and oxygen tension.

摘要

线粒体中超氧化物的产生是细胞内活性氧物质的一个重要来源,可能导致或促成衰老和与衰老相关的疾病。哺乳动物线粒体中超氧化物产生的 7 个主要部位已被广泛认可。按最大产能从高到低的顺序依次为:复合体 I(部位 IQ)和复合体 III(部位 IIIQo)的泛醌结合部位、甘油 3-磷酸脱氢酶、复合体 I 中的黄素(部位 IF)、电子传递黄素蛋白:Q 氧化还原酶(ETFQOR)、脂肪酸β氧化、以及丙酮酸和 2-氧戊二酸脱氢酶。这些部位没有一个得到充分的描述,有些部位我们只有粗略的信息。部位的拓扑结构很重要,因为它决定了一个部位是否会在线粒体基质中产生超氧化物,并能够损伤线粒体 DNA。所有部位都在线粒体基质中产生超氧化物;部位 IIIQo 和甘油 3-磷酸脱氢酶也会向膜间腔中产生超氧化物。在没有电子传递抑制剂的情况下,每个部位对分离线粒体、细胞或体内线粒体活性氧物质生成的相对贡献是未知的,并且可能因物种、组织、底物、能量需求和氧张力而有很大差异。