Redox Regulation of DJ-1 Function
Redox Regulation of DJ-1 Function
批准号:
8703718
负责人:
Mark A. Wilson
金额:
$26.7万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-08-01 至 2016-07-31
关键词:
AffectAffinityAging-Related ProcessAnimal ModelAnimalsApoptosisBindingBiochemicalBiochemistryBiological ModelsCell Culture TechniquesCellsCommunitiesComplementCysteineCytoprotectionDataDiseaseDrosophila genusDrosophila melanogasterEscherichia coliEtiologyEukaryotaGenerationsGeneticGoalsHomeostasisHomologous GeneHumanKnock-outKnowledgeLeadMaintenanceMalignant NeoplasmsMessenger RNAMitochondriaModificationMolecularMutationNeurodegenerative DisordersOrganismOxidation-ReductionOxidative RegulationOxidative StressPARK7 proteinParkinsonian DisordersPathogenesisPlayPost-Translational Protein ProcessingProkaryotic CellsProtein FamilyProteinsProteomePublicationsRNA BindingRegulationResearchRoentgen RaysRoleScientistStrokeStructureStructure-Activity RelationshipSystemTestingTherapeuticTranscriptTranslationsWorkX-Ray Crystallographybasebiological adaptation to stresscell typecysteine sulfinic aciddesigneffective therapyexpectationexperiencehuman diseaseimprovedin vivoinnovationinsightmacromoleculemembermitochondrial dysfunctionoxidationprotein functionpublic health relevancesensortherapy development
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Oxidative stress and mitochondrial dysfunction are centrally involved in the etiology of several diseases and in the normal process of aging. The protein DJ-1 is an oxidative stress response protein whose absence or dysregulation has been implicated in parkinsonism, cancer, and stroke. DJ-1 can robustly protect cells against multiple forms of oxidative stress and thereby confer protection against degeneration that can lead to disease. The molecular mechanism(s) of DJ-1's action, however, remains unclear. DJ-1 contains a functionally essential cysteine residue whose oxidation is hypothesized to regulate its cytoprotective function. We will investigate the mechanism by which DJ-1 senses and responds to oxidative stress by accomplishing three specific aims. The first aim will investigate the role of DJ-1 cysteine oxidation in the protection against oxidative stress in the Drosophila animal model system. We will combine X-ray crystallography, biochemistry, and Drosophila genetics to establish a powerful animal model for the redox regulation of DJ-1 function. The second aim will determine the structure-function relationships for an established mRNA binding activity of DJ-1. The results will be used to test the hypothesis that conserved structural features near the oxidized cysteine integrate the RNA binding and redox sensing functions of DJ-1. The third aim will use a prokaryotic model system to investigate the evolutionarily conserved mechanism of DJ-1 protective function. The results will be used to test existing hypotheses about the conservation of regulatory cysteine oxidation in DJ-1 function as well as discover new functions for DJ-1. In total, the proposed research will provide a comprehensive molecular basis for understanding the oxidative regulation and pathogenic disruption of DJ-1 function. Ultimately, the results of this research will be used to design a new generation of therapeutics that enhance the protective function of DJ-1 in vulnerable cell types.
PUBLIC HEALTH RELEVANCE: Oxidative stress and mitochondrial dysfunction are centrally involved in several human diseases. Major recent advances have identified DJ-1 as a protein that confers robust protection against oxidative stress. The precise biochemical function of DJ-1, however, remains uncertain. The long-term goal of this proposal is to determine the biochemical functions of DJ-1 that confer protection against oxidative stress and with the goal of developing therapies that improve the protective function of DJ-1.
期刊论文(5)
专著(0)
科研奖励(0)
会议论文
Metabolic role for yeast DJ-1 superfamily proteins.
酵母 DJ-1 超家族蛋白的代谢作用。
DOI:
10.1073/pnas.1405511111
发表时间:
2014
期刊:
Proceedings of the National Academy of Sciences of the United States of America
影响因子:
11.1
作者:
[Wilson,MarkA]
通讯作者:
Wilson,MarkA
DOI:
10.1111/febs.12004
发表时间:
2012-11
期刊:
The FEBS journal
影响因子:
--
作者:
[Madzelan P, Labunska T, Wilson MA]
通讯作者:
Wilson MA
Time-Resolved X-ray Crystallography of Dynamics in Cysteine-Dependent Enzymes
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批准号:10684770
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项目类别:
-
资助金额:$29.6万
-
财政年份:2020
-
负责人:Mark A. Wilson
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依托单位:
Time-Resolved X-ray Crystallography of Dynamics in Cysteine-Dependent Enzymes
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批准号:10259757
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项目类别:
-
资助金额:$29.6万
-
财政年份:2020
-
负责人:Mark A. Wilson
-
依托单位:
Time-Resolved X-ray Crystallography of Dynamics in Cysteine-Dependent Enzymes
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批准号:10099548
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项目类别:
-
资助金额:$29.6万
-
财政年份:2020
-
负责人:Mark A. Wilson
-
依托单位:
Time-Resolved X-ray Crystallography of Dynamics in Cysteine-Dependent Enzymes
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批准号:10469510
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项目类别:
-
资助金额:$29.6万
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财政年份:2020
-
负责人:Mark A. Wilson
-
依托单位:
Redox Regulation of DJ-1 Function
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批准号:8516532
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项目类别:
-
资助金额:$25.79万
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财政年份:2010
-
负责人:Mark A. Wilson
-
依托单位:
Redox Regulation of DJ-1 Function
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批准号:7865772
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项目类别:
-
资助金额:$27.05万
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财政年份:2010
-
负责人:Mark A. Wilson
-
依托单位:
Redox Regulation of DJ-1 Function
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批准号:8302424
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项目类别:
-
资助金额:$26.74万
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财政年份:2010
-
负责人:Mark A. Wilson
-
依托单位:
Redox Regulation of DJ-1 Function
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批准号:8118584
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项目类别:
-
资助金额:$26.76万
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财政年份:2010
-
负责人:Mark A. Wilson
-
依托单位:
海外基金