Regulation of NADH:ubiquinone oxidoreductase (complexI)

NADH 的调节：泛醌氧化还原酶（复合物 I）

• 批准号: 7233538
• 负责人: Andrei D Vinogradov
• 金额: $ 3.01万
• 依托单位: MOSCOW STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-04-01 至 2010-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7233538
• 关键词: Aerobic; Affect; Amino Acids; Applications Grants; Award; Binding; Binding Sites; Biochemical; Bioenergetics; Biological Assay; Biological Models; Brain; Cell Respiration; Cell membrane; Cells; Collaborations; Complex; Condition; Coupled; Data; Defect; Development; Electrochemistry; Electron Spin Resonance Spectroscopy; Electron Transport; Enzymes; Fatty Acids; Flavin Mononucleotide; Frequencies; Genes; Genetic Transcription; Grant; Guidelines; Heart; Heme; Homologous Gene; Human; Hydrogen Peroxide; Individual; Iron; Ischemia; Kinetics; Laboratories; Ligands; Light; Membrane; Metabolic; Mitochondria; Modeling; Molecular; Moscow; Mutagenesis; NADH; NADH dehydrogenase (ubiquinone); Neurodegenerative Disorders; Non-Insulin-Dependent Diabetes Mellitus; Nonesterified Fatty Acids; Nucleotides; Operon; Oxidation-Reduction; Oxygen; Paraganglioma; Parents; Parkinson Disease; Pathology; Pheochromocytoma; Physiologic pulse; Physiological; Physiological reperfusion; Play; Post-Translational Protein Processing; Preparation; Production; Prokaryotic Cells; Property; Proteins; Protons; Pulse taking; Quinones; Rattus; Reactive Oxygen Species; Regulation; Reperfusion Therapy; Research; Resolution; Respiratory Chain; Roentgen Rays; Role; San Francisco; Scaffolding Protein; Scientist; Site; Spectroscopy, Fourier Transform Infrared; Spectrum Analysis; Structure; Submitochondrial Particles; Succinate Dehydrogenase; Sulfur; Superoxides; Techniques; Testing; Thermus; Thermus thermophilus; Time; Tissues; Ubiquinone; benzoquinone; design; inhibitor/antagonist; mutant; oxidation; research study; respiratory protein; tumor; ubisemiquinone

DESCRIPTION (provided by applicant): The mitochondrial NADH:ubiquinone oxidoreductase (Complex I) is a key essential component of the bioenergetic machinery in all aerobic cells. The mammalian Complex I is the largest component of mitochondrial respiratory chain; composed of at least 46 individual subunits and up to 10 distinct redox centers. The structural complexity of the enzyme is consistent with its varied catalytic and regulatory properties. Two slowly equilibrating forms of the enzyme, A (active) and D (deactive) exist under given metabolic conditions and each form has different sensitivity to inhibitory and/or activating ligands. This project is to extend our previous collaborative studies on the Complex I A/D transition at the molecular and physiological level. The mechanisms responsible for the inhibitory effects of free fatty acids on Complex I and other physiologically relevant membrane perturbing compounds will be studied. The inhibitory and/or activating effects of fatty acids and their derivatives will be correlated with their modulating effects on the A/D transition and superoxide production by Complex I. These studies will be done in intact mitochondria and inside-out tightly coupled submitochondrial particles. Experiments designed to identify other matrix-located redox enzyme(s) capable of superoxide and hydrogen peroxide production as related to Complex I activity are planned. This research will be primarily done in the Russian laboratory. The results obtained will be used as a guideline for further elaboration at the physiological level of the A/D transition using a model of ischemia/reperfusion in Langendorf-perfused rat hearts, a technique well developed in the U.S. laboratory. The U.S. laboratory will assist the Russian scientists with the Langendorf-perfused heart model and in identifying particular subunits of Complex I that are involved in the regulatory A/D transition. A two-nucleotide binding site(s) model proposed by the Russian group will be tested with the help of the US laboratory by use of a new tight nucleotide-binding site-directed inhibitor recently discovered in the U.S. laboratory. The biomedical significance of this project is to identify the key players involved in regulation of cellular respiration and in development of mitochondria-related pathologies such as occur during oxygen supply deficiency, type 2 diabetes, and neurodegenerative diseases. Defects in Complex I have been shown to contribute to Parkinson's disease and these studies may shed light on how this important metabolic enzyme is regulated.

描述（由申请人提供）：线粒体NADH：泛醌氧化还原酶（复合物I）是所有需氧细胞中生物能量机制的关键必需组分。哺乳动物复合物I是线粒体呼吸链的最大组成部分;由至少46个单独的亚基和多达10个不同的氧化还原中心组成。该酶的结构复杂性与其不同的催化和调节特性是一致的。在给定的代谢条件下，存在两种缓慢平衡的酶形式，A（活性）和D（失活），每种形式对抑制和/或活化配体具有不同的敏感性。该项目是在分子和生理水平上扩展我们以前对复合物I A/D转换的合作研究。将研究游离脂肪酸对复合物I和其他生理相关膜扰动化合物的抑制作用的机制。脂肪酸及其衍生物的抑制和/或活化作用将与它们对A/D转换和复合物I产生超氧化物的调节作用相关。这些研究将在完整的线粒体和由内而外紧密耦合的亚线粒体颗粒中进行。计划进行旨在鉴定与复合物I活性相关的能够产生超氧化物和过氧化氢的其他基质定位的氧化还原酶的实验。这项研究将主要在俄罗斯实验室进行。所获得的结果将被用作进一步阐述在生理水平上的A/D转换使用模型的缺血/再灌注在Langendorf灌注大鼠心脏，在美国实验室开发的技术的指导方针。美国实验室将协助俄罗斯科学家进行Langendorf灌注心脏模型，并鉴定参与调节A/D转换的复合物I的特定亚基。俄罗斯小组提出的一个两核苷酸结合位点模型将在美国实验室的帮助下，使用美国实验室最近发现的一种新的紧密核苷酸结合位点定向抑制剂进行测试。该项目的生物医学意义是确定参与细胞呼吸调节和与呼吸相关的病理学发展的关键参与者，如氧气供应不足，2型糖尿病和神经退行性疾病。复合物I的缺陷已被证明有助于帕金森病，这些研究可能揭示了这种重要的代谢酶是如何调节的。