Oxidative Thiol Modifications and Aging
Oxidative Thiol Modifications and Aging
批准号:
7348344
负责人:
Ursula H. Jakob
金额:
$27.48万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-02-15 至 2012-01-31
关键词:
Activities of Daily LivingAgeAgingAging-Related ProcessAntioxidantsCaenorhabditis elegansCellsCharacteristicsConditionCysteineDevelopmentEukaryotic CellFree RadicalsIn VitroKnowledgeLifeLinkLocationLongevityMetabolicModificationMonitorNitrogenOrganismOxidantsOxidation-ReductionOxidative StressOxygenPhysiologicalPhysiologyPlayPost-Translational Protein ProcessingProteinsReactive Nitrogen SpeciesReactive Oxygen SpeciesReadingReporterResearch PersonnelRoleSaccharomyces cerevisiaeSignal PathwaySpecific qualifier valueSpecificityStagingStressSulfhydryl CompoundsTechniquesTestingTimeTissuesYeastsbaseimprovedin vivomutantnanoswitchnovel strategiesoxidationresearch studysensortheoriestool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The free radical theory of aging postulates that the accumulation of reactive oxygen and nitrogen species is causally linked to the progressive decline in the functional capacity of aging organisms. We have now developed the tools to test this hypothesis. We will detect, monitor and specify which oxidative stress conditions exist in aging organisms. We will accomplish this by utilizing the unique characteristics of oxidative protein thiol modifications: high sensitivity to the presence of small amounts of oxidants, high specificity to distinct reactive oxidants and reversibility both in vitro and in vivo. We are able to quantitatively describe changes in the thiol oxidation status of hundreds of proteins in a single experiment. This allows us to identify proteins that are significantly thiol-modified during chronological yeast aging and to define the type(s) of reactive oxygen or nitrogen species that develop during aging. Wild type and longevity mutants of S. cerevisiae will be used to investigate if a link exists between the onset, type(s) and extent of oxidative stress that cells encounter, and the life span of the organism. We will quantitatively describe oxidative protein modifications at early stages of yeast aging. This will reveal proteins that are particularly sensitive to early changes in the cellular redox status. The functional alteration of these proteins might be responsible for changes observed in metabolic and signaling pathways of chronologically aging yeast cells. We have developed fluorescent-based in vivo redox sensors that we will use to detect reactive oxygen species in S. cerevisiae and C. elegans. This is a very novel approach, which provides us with the unique opportunity to obtain a real-time picture of the oxidative stress conditions that develop in cells and tissues as an organism ages. The knowledge that we will gain from our studies could form the basis for the development of more specific antioxidants that combat these oxidants in vivo and possibly extend longevity.
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2015 Stress Proteins in Growth, Development and Disease GRC
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Polyphosphate - A Novel Member of the Proteostasis Network
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Polyphosphate - A Novel Member of the Proteostasis Network
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批准号:9118242
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Investigation of developmental peroxide generation as an important lifespan-deter
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财政年份:2014
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Investigation of developmental peroxide generation as an important lifespan-deter
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财政年份:2012
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依托单位:
Characterization of bleach-specific transcriptional regulators in bacteria
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批准号:8227038
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资助金额:$22.8万
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财政年份:2012
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依托单位:
Oxidative Thiol Modifications and Aging
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批准号:7211988
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项目类别:
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资助金额:$27.19万
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财政年份:2007
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依托单位:
Oxidative Thiol Modifications and Aging
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批准号:7794846
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项目类别:
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资助金额:$27.21万
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财政年份:2007
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依托单位:
Oxidative Thiol Modifications and Aging
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批准号:8027731
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项目类别:
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资助金额:$26.15万
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财政年份:2007
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依托单位:
Oxidative Thiol Modifications and Aging
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批准号:7569467
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财政年份:2007
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负责人:Ursula H. Jakob
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依托单位:
Functional Analysis of Hsp33-a Redox Regulated Chaperone
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批准号:6698043
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项目类别:
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资助金额:$21.45万
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财政年份:2003
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依托单位:
Functional Analysis of Hsp33-a Redox Regulated Chaperone
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批准号:6576740
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财政年份:2003
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负责人:Ursula H. Jakob
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依托单位:
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