Catalytic Properties of Cytochrome Oxidase

细胞色素氧化酶的催化特性

• 批准号: 7922382
• 负责人: DENIS L. ROUSSEAU
• 金额: $ 12.13万
• 依托单位: ALBERT EINSTEIN COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-15 至 2010-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7922382
• 关键词: Active Sites; Bacteria; Binding; Binding Sites; Catalytic Domain; Cell Respiration; Chemistry; Complex; Copper; Coupled; Coupling; Electron Spin Resonance Spectroscopy; Electron Transport; Electrons; Engineering; Enzymes; Freezing; Goals; Heme; Hemeproteins; Home environment; Inner mitochondrial membrane; Label; Lasers; Life; Ligand Binding; Light; Membrane; Methods; Modeling; Monitor; Mutagenesis; Myoglobin; Nature; Optics; Organ; Oxidases; Oxidation-Reduction; Oxidative Phosphorylation; Oxygen; Pathway interactions; Peripheral; Physeteridae; Physiology; Play; Population; Process; Property; Proteins; Proton Pump; Protons; Reaction; Rest; Role; Site; Spectrum Analysis; Techniques; Testing; Time; absorption; cytochrome c oxidase; link protein; mutant; photolysis; rapid technique; research study

DESCRIPTION (provided by applicant): The major goal of this project is to determine the basic functional mechanism of cytochrome c oxidase (CcO), the terminal enzyme in the electron transfer chain. CcO is membrane-bound and has the dual function of reducing O2 to H2O to maintain electron flow to enable oxidative phosphorylation, and of coupling the oxygen reduction chemistry to proton translocation across the inner mitochondrial membrane, to generate a proton gradient. The enzyme plays an indispensable role in mammalian physiology because essentially all vital organs depend on aerobic metabolism. Despite years of intensive studies on CcO, the understanding of its catalytic processes is still incomplete and its mechanism of proton translocation remains unclear. We propose a variety of experiments to delineate the oxygen reduction chemistry and aim to shed new light on the coupled proton translocation. In order to identify the catalytic intermediates, new rapid mixing, laser photolysis and freeze trapping techniques will be applied to studies of both the mammalian and the bacterial forms of the enzyme. Full characterization will be done with resonance Raman scattering, optical absorption and electron paramagnetic resonance spectroscopies. One of the major focuses will be to determine the properties of the still controversial short-lived peroxo and ferryl intermediates. Resonance Raman and optical absorption spectroscopy will also be used in conjunction with a home-built continuous flow apparatus to monitor the time-dependent population of the reactive intermediates present during single as well as multiple turnover of the enzyme. To determine the role of specific residues in the functional processes of the enzyme, site directed mutants of CcO from bacteria will be expressed and analyzed by this multifaceted approach. In addition, the oxygen chemistry in a new class of model complexes, a mutant myoglobin with a binuclear center engineered in it to mimic the catalytic site of CcO, will be studied to elucidate the role of the binuclear heme-copper center. The energy transduction and proton translocation mechanism of CcO will be constructed, tested and refined.

描述（由申请人提供）：该项目的主要目标是确定电子传递链末端酶细胞色素c氧化酶（CcO）的基本功能机制。 CcO 是膜结合的，具有将 O2 还原为 H2O 以维持电子流以实现氧化磷酸化的双重功能，以及将氧还原化学与穿过线粒体内膜的质子易位耦合以产生质子梯度的双重功能。这种酶在哺乳动物生理学中起着不可或缺的作用，因为基本上所有重要器官都依赖于有氧代谢。尽管对CcO进行了多年的深入研究，但对其催化过程的了解仍然不完整，其质子易位机制仍不清楚。我们提出了各种实验来描述氧还原化学，并旨在为耦合质子易位提供新的线索。为了鉴定催化中间体，新的快速混合、激光光解和冷冻捕获技术将应用于哺乳动物和细菌形式的酶的研究。完整的表征将通过共振拉曼散射、光学吸收和电子顺磁共振光谱来完成。主要焦点之一是确定仍然存在争议的短寿命过氧化氢和弗瑞尔中间体的特性。共振拉曼和光吸收光谱也将与自制的连续流动装置结合使用，以监测酶的单次和多次周转期间存在的反应中间体的时间依赖性数量。为了确定特定残基在酶功能过程中的作用，将通过这种多方面的方法表达和分析来自细菌的 CcO 定点突变体。此外，我们还将研究一类新型模型复合物（一种具有双核中心的突变肌红蛋白，旨在模拟 CcO 催化位点）中的氧化学，以阐明双核血红素-铜中心的作用。 CcO的能量转换和质子易位机制将被构建、测试和完善。

项目成果

EPR characterization of ascorbyl and sulfur dioxide anion radicals trapped during the reaction of bovine Cytochrome c Oxidase with molecular oxygen.

牛细胞色素 c 氧化酶与分子氧反应期间捕获的抗坏血酸和二氧化硫阴离子自由基的 EPR 表征。

• DOI: 10.1016/j.jmr.2009.12.017
• 发表时间: 2010-04
• 期刊: Journal of magnetic resonance
• 影响因子: 2.2
• 作者: Yu MA;Egawa T;Yeh SR;Rousseau DL;Gerfen GJ
• 通讯作者: Gerfen GJ

Electron transfer pathways in cytochrome c oxidase.

细胞色素 c 氧化酶中的电子转移途径。

• DOI: 10.1016/j.bbabio.2011.03.003
• 发表时间: 2011-10
• 期刊: Biochimica et biophysica acta
• 作者: Fatima Lucas, M.;Rousseau, Denis L.;Guallar, Victor
• 通讯作者: Guallar, Victor

Radical formation in cytochrome c oxidase.

细胞色素c氧化酶中的自由基形成。

• 发表时间: 2011-10
• 作者: Yu, Michelle A;Egawa, Tsuyoshi;Shinzawa;Yoshikawa, Shinya;Yeh, Syun;Rousseau, Denis L;Gerfen, Gary J
• 通讯作者: Gerfen, Gary J

Two tyrosyl radicals stabilize high oxidation states in cytochrome C oxidase for efficient energy conservation and proton translocation.

两个酪氨酰自由基稳定细胞色素 C 氧化酶中的高氧化态，以实现有效的能量保存和质子易位。

• 发表时间: 2012-03-14
• 影响因子: 15
• 作者: Yu, Michelle A;Egawa, Tsuyoshi;Shinzawa;Yoshikawa, Shinya;Guallar, Victor;Yeh, Syun;Rousseau, Denis L;Gerfen, Gary J
• 通讯作者: Gerfen, Gary J

The rate-limiting step in O(2) reduction by cytochrome ba(3) from Thermus thermophilus.

嗜热栖热菌细胞色素 ba(3) 还原 O(2) 的限速步骤。

• 发表时间: 2012-04
• 作者: Egawa, Tsuyoshi;Chen, Ying;Fee, James A.;Yeh, Syun-Ru;Rousseau, Denis L.
• 通讯作者: Rousseau, Denis L.