Energy Transduction in Cytochrome Oxidase
Energy Transduction in Cytochrome Oxidase
批准号:
8249049
负责人:
SHELAGH M FERGUSON-MILLER
金额:
$39.92万
依托单位国家:
美国
项目类别:
财政年份:
1979
资助国家:
美国
项目状态:
已结题
起止时间:
1979-07-01 至 2015-03-31
关键词:
AffectAgingAreaBacteriaBilirubinBindingBinding SitesBiological AssayBiological ModelsBreathingCellsCessation of lifeClinicalCollaborationsComplexComputer SimulationCrystallizationCrystallographyDiabetes MellitusDiseaseElectron TransportEnergy MetabolismEngineeringEnzymesGene FusionGoalsGrantIn VitroKineticsKnowledgeLifeLigandsLipid BindingLipidsMalignant NeoplasmsMammalsMass Spectrum AnalysisMembrane ProteinsMetabolicMetabolic DiseasesMetabolismMethodsMitochondriaMolecularMolecular ConformationMutationNeurologic DysfunctionsObesityOutcomeOxidasesOxidation-ReductionOxygenPharmaceutical PreparationsPhasePhysiologicalPhytanic AcidPositioning AttributeProcessProductionProtein EngineeringProton PumpRegulationResearchResearch SupportResolutionRhodobacterRhodobacter sphaeroidesRobotRoboticsRoleScreening procedureSiteSolutionsSteroidsStructureTestingWaterWorkage relatedanalogbasecomputerized toolscytochrome c oxidasedesignenzyme structureflexibilitymutantnovelpreventprogramsprotoporphyrin IXpublic health relevanceresearch studytool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The importance of developing a better understanding of the function and regulation of cytochrome c oxidase has become increasingly apparent, given its decisive influence on mitochondrial metabolism and the central role of mitochondria in controlling cell life and death. Research supported by this grant has led us to a new perspective on this complex energy conserving machine, derived from a number of new high resolution structures of the enzyme from the mitochondrial model system, Rhodobacter sphaeroides. These reveal previously unobserved changes in conformation associated with altered redox state, and the presence of lipid and steroid binding sites conserved in bacteria and mammals. This proposal is aimed at determining the significance of the novel structural findings through further crystallographic efforts designed to obtain new and higher resolution crystal forms, and through studies of the effects of lipidic ligands on activity, stability and efficiency of oxidase. The Specific Aims are: 1) to generate additional crystal forms of two and four subunit Rhodobacter oxidase, using molecular engineering strategies and robotic crystal screening; 2) to create, characterize and crystallize mutants that facilitate the trapping of novel catalytic intermediates or that restrain flexibility, to look for new conformational states and test the importance of conformational change; 3) to screen for alternative ligands of a steroid binding site, with potential physiological significance, or inhibitory or stabilizing effects. A major tool in these studies will be crystallography, but our ability to comprehensively analyze oxidase function and spectral features, including on-line crystal spectra, will be crucial to interpreting the structural findings. The expected outcome is a new level of understanding of the molecular mechanism of energy conversion in cytochrome oxidase, including the role of conformational change in gating and efficiency, and the regulatory effects of lipidic ligands. The long term goal is to better understand the involvement of cytochrome oxidase in metabolic disease states including cancer, obesity, diabetes and aging, through structure/function analysis and the discovery of compounds that are physiological effectors, crystallization aids, mechanistic probes, or precursors to drugs that can modulate oxidase activity.
PUBLIC HEALTH RELEVANCE: Cytochrome c oxidase is a critical player in normal physiological function, consuming more than 90% of the oxygen we breathe and being directly involved in the production of most of the energy we use to support all life processes; the goal of this research program is to develop a better understanding of cytochrome oxidase function and regulation. The importance of this objective has become increasingly apparent, given the decisive influence of cytochrome oxidase on mitochondrial energy metabolism and the central role of mitochondria in controlling cell life and death. The long term goal is to better understand the involvement of cytochrome oxidase in metabolic disease states including cancer, obesity, diabetes and aging, through structure/ function analysis and the discovery of new compounds that are physiological effectors, crystallization aids, mechanistic probes, or precursors to drugs that can modulate oxidase activity and efficiency.
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批准号:9759746
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项目类别:
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资助金额:$22.68万
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财政年份:2018
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
INVESTIGATION OF SPECTRAL CHANGES OF CYTOCHROME C OXIDASE UPON X-RAY IRRADIATION
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批准号:8171992
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项目类别:
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资助金额:$0.73万
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财政年份:2010
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
INVESTIGATION OF SPECTRAL CHANGES OF CYTOCHROME C OXIDASE UPON X-RAY IRRADIATION
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批准号:7956837
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项目类别:
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资助金额:$0.47万
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财政年份:2009
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
ENERGY TRANSDUCTION IN CYTOCHROME OXIDASE
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批准号:7930214
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项目类别:
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资助金额:$8.5万
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财政年份:2009
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
INVESTIGATION OF SPECTRAL CHANGES OF CYTOCHROME C OXIDASE UPON X-RAY IRRADIATION
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批准号:7956801
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项目类别:
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资助金额:$0.94万
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财政年份:2009
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
STRUCTURAL ANALYSIS OF THE MEMBRANE METALLOPROTEIN CYTOCHROME C OXIDASE IN
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批准号:7726019
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项目类别:
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资助金额:$0.79万
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财政年份:2008
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
HIGH PRESSURE COOLING OF CYTOCHROME C OXIDASE
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批准号:7357733
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项目类别:
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资助金额:$1.06万
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财政年份:2006
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
SUBSTRATE DOCKING IN CYTOCHROME C OXIDASE
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批准号:6316674
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项目类别:
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资助金额:$10.47万
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财政年份:2000
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
SUBSTRATE DOCKING IN CYTOCHROME C OXIDASE
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批准号:6107869
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项目类别:
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资助金额:$10.47万
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财政年份:1999
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
SUBSTRATE DOCKING IN CYTOCHROME C OXIDASE
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批准号:6271921
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项目类别:
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资助金额:$11.58万
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财政年份:1998
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
OXYGEN UTILIZING MEMBRANE HEME PROTEINS
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批准号:6519864
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项目类别:
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资助金额:$90.48万
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财政年份:1998
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
1997 GORDON CONFERENCE ON BIOENERGETICS
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批准号:2385167
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项目类别:
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资助金额:$0.4万
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财政年份:1997
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
ENERGY TRANSDUCTION IN CYTOCHROME OXIDASE
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批准号:6518995
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项目类别:
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资助金额:$30.71万
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财政年份:1979
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
ORGANIZATION AND CONTROL OF ELECTRON TRANSFER CHAINS
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批准号:3274383
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项目类别:
-
资助金额:$14.7万
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财政年份:1979
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
ORGANIZATION AND CONTROL OF ELECTRON TRANSFER CHAINS
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批准号:3274380
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项目类别:
-
资助金额:$2.45万
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财政年份:1979
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
ORGANIZATION AND CONTROL OF ELECTRON TRANSFER CHAINS
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批准号:3274385
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项目类别:
-
资助金额:$14.29万
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财政年份:1979
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负责人:SHELAGH M FERGUSON-MILLER
-
依托单位:
ORGANIZATION AND CONTROL OF ELECTRON TRANSFER CHAINS
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批准号:3274378
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项目类别:
-
资助金额:$12.65万
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财政年份:1979
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负责人:SHELAGH M FERGUSON-MILLER
-
依托单位:
ORGANIZATION AND CONTROL OF ELECTRON TRANSFER CHAINS
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批准号:3274382
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项目类别:
-
资助金额:$10.15万
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财政年份:1979
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
Energy Transduction in Cytochrome Oxidase
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批准号:8448773
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项目类别:
-
资助金额:$38.53万
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财政年份:1979
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
ENERGY TRANSDUCTION IN CYTOCHROME OXIDASE
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批准号:2444498
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项目类别:
-
资助金额:$23.12万
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财政年份:1979
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负责人:SHELAGH M FERGUSON-MILLER
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依托单位:
海外基金