Unraveling Cell Death via Top-Down/Bottom-Up Proteomics
Unraveling Cell Death via Top-Down/Bottom-Up Proteomics
批准号:
7392170
负责人:
CHENG S LEE
金额:
$27.54万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-04-01 至 2010-03-31
关键词:
AddressAdsorptionAnimal GeneticsAnimalsApoptosisAutoimmunityBiochemicalBiological MarkersBiological ModelsBlood capillariesCapillary ElectrophoresisCaseinsCaspaseCell DeathCellsCessation of lifeChromatographyComplexComputersCoupledCouplingCysteine ProteaseDNA Microarray ChipDNA Microarray formatDataDatabasesDefectDepositionDetectionDetergentsDevelopmentDigestionDimensionsDiseaseDrosophila genusDrosophila melanogasterElectrospray IonizationEmbryoEmbryo DeathsEmbryonic DevelopmentEquipmentEvaluationExhibitsFamilyFigs - dietaryFluorescenceFractionationGelGene Expression ProfileGenesGeneticGenetic TranscriptionGenomeGoalsGroupingHeadHumanHydrophobicityIn SituIndividualInvestigationIsoelectric FocusingLaboratoriesLeadLinkLiquid ChromatographyMalignant NeoplasmsManualsMass Spectrum AnalysisMeasuresMembraneMembrane ProteinsMethodologyMethodsMicroinjectionsModelingModificationMolecularMutationNatureNumbersOperative Surgical ProceduresOrganismPancreatic ribonucleasePathway interactionsPatternPeptidesPerformancePhasePhysiologicalPlayPolyacrylamide Gel ElectrophoresisPopulationPost-Translational Protein ProcessingPrecipitationProceduresProcessProtein AnalysisProtein Sequence AnalysisProteinsProteolysisProteomeProteomicsRNARadiationRangeRegulationReportingReproducibility of ResultsResearchResolutionRoleRunningSalivary GlandsSamplingShotgunsSodium Dodecyl SulfateSolidSolutionsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationSpeedSteroidsSystemTechniquesTechnologyTimeTissuesTodayTrypsinTwo-Dimensional Polyacrylamide Gel ElectrophoresisValidationYeastsbasecapillarycell killingelectric fieldflygel electrophoresisgenetic regulatory proteinimprovedinformation gatheringinnovationinstrumentinstrumentationinterestmRNA Differential Displaysmass spectrometermolecular massnanoscalenovelnumb proteinpreventprofessorprotein expressionsizetandem mass spectrometrytool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Apoptosis and autophagic cell death are the two most prominent forms of programmed cell death that occur during animal development. While much is known about the regulation of apoptosis, relatively little is known about the mechanisms underlying autophagic cell death, and what mechanism and biochemical changes distinguish these most prominent forms of physiological cell killing. Drosophila embryos and salivary glands are an ideal system to study apoptosis and autophagic programmed cell death. The mass of embryos and salivary gland cells enable rapid purification and separation from other tissues, providing one of the few higher animal genetic systems where molecular and biochemical approaches can be used to study a purified population of dying cells in the context of a developing organism. These attributes argue that studies of Drosophila apoptosis and autophagic cell death will lead to the identification of new cell death proteins, and provide an excellent system to study their function. The programmed cell death genetic pathway is extremely conserved between fruit flies and humans, indicating that studies of cell death in Drosophila will be directly relevant to higher organisms.
Our research goal is to develop, optimize, and apply innovative proteome technology for the comprehensive analysis of protein profiles during programmed cell death. By using the fruit fly Drosophila melanogaster as a model system, these proteome studies will explore pathways and identify biomarkers associated with Caspase activation during cell death in developing animals. This challenge will be addressed through the development and application of a capillary-based and integrated top-down/bottom-up multidimensional separation platform capable of ultrahigh resolution of intact proteins, followed by in situ proteolytic digestion of size-resolved proteins, high throughput peptide separation, and ultrasensitive peptide/protein identification. The combined strength of Drosophila genetics and the proposed innovative bioanalytical technologies enables investigation into the regulation of programmed cell death at the genome-wide level including the expression of proteins on a global scale.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1021/pr7006768
发表时间:
2008-02
期刊:
Journal of proteome research
影响因子:
4.4
作者:
[Haifeng Xu;Li Yang;Weijie Wang;S. Shi;Cheng Liu;Y. Liu;X. Fang;C. Taylor;Cheng S. Lee;B. Balgley]
通讯作者:
Haifeng Xu;Li Yang;Weijie Wang;S. Shi;Cheng Liu;Y. Liu;X. Fang;C. Taylor;Cheng S. Lee;B. Balgley
DOI:
10.1002/elps.200900367
发表时间:
2009-12
期刊:
ELECTROPHORESIS
影响因子:
2.9
作者:
[Fang, Xueping, Balgley, Brian M., Wang, Weijie, Park, Deric M., Lee, Cheng S.]
通讯作者:
Lee, Cheng S.
Development of Nanoproteomic Technologies
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批准号:8474798
-
项目类别:
-
资助金额:$18.09万
-
财政年份:2011
-
负责人:CHENG S LEE
-
依托单位:
Development of Nanoproteomic Technologies
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批准号:8160643
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项目类别:
-
资助金额:$18.75万
-
财政年份:2011
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负责人:CHENG S LEE
-
依托单位:
Development of Nanoproteomic Technologies
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批准号:8321507
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项目类别:
-
资助金额:$18.75万
-
财政年份:2011
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负责人:CHENG S LEE
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依托单位:
CITP-Based Selective Tissue Proteome Enrichment
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批准号:8308672
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项目类别:
-
资助金额:$22.15万
-
财政年份:2010
-
负责人:CHENG S LEE
-
依托单位:
CITP-Based Selective Tissue Proteome Enrichment
-
批准号:7942540
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项目类别:
-
资助金额:$19.58万
-
财政年份:2010
-
负责人:CHENG S LEE
-
依托单位:
CITP-Based Selective Tissue Proteome Enrichment
-
批准号:8134976
-
项目类别:
-
资助金额:$22.15万
-
财政年份:2010
-
负责人:CHENG S LEE
-
依托单位:
Unraveling Cell Death via Top-Down/Bottom-Up Proteomics
-
批准号:7045979
-
项目类别:
-
资助金额:$25.75万
-
财政年份:2005
-
负责人:CHENG S LEE
-
依托单位:
Unraveling Cell Death via Top-Down/Bottom-Up Proteomics
-
批准号:7216414
-
项目类别:
-
资助金额:$27.54万
-
财政年份:2005
-
负责人:CHENG S LEE
-
依托单位:
Unraveling Cell Death via Top-Down/Bottom-Up Proteomics
-
批准号:6901316
-
项目类别:
-
资助金额:$27.29万
-
财政年份:2005
-
负责人:CHENG S LEE
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依托单位:
2D PROTEIN ANALYSIS USING MICROCHIP MASS SPECTROMETRY
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批准号:2830132
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项目类别:
-
资助金额:$10.64万
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财政年份:1999
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负责人:CHENG S LEE
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依托单位:
2D PROTEIN ANALYSIS USING MICROCHIP MASS SPECTROMETRY
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批准号:6175262
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项目类别:
-
资助金额:$10.62万
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财政年份:1999
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负责人:CHENG S LEE
-
依托单位:
THERAPEUTIC DRUG MONITORING BY CAPILLARY IMMUNOPHORESIS
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批准号:2762434
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项目类别:
-
资助金额:$9.38万
-
财政年份:1995
-
负责人:CHENG S LEE
-
依托单位:
THERAPEUTIC DRUG MONITORING BY CAPILLARY IMMUNOPHORESIS
-
批准号:2192553
-
项目类别:
-
资助金额:$11.92万
-
财政年份:1995
-
负责人:CHENG S LEE
-
依托单位:
THERAPEUTIC DRUG MONITORING BY CAPILLARY IMMUNOPHORESIS
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批准号:2459668
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项目类别:
-
资助金额:$0.8万
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财政年份:1995
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负责人:CHENG S LEE
-
依托单位:
THERAPEUTIC DRUG MONITORING BY CAPILLARY IMMUNOPHORESIS
-
批准号:2192554
-
项目类别:
-
资助金额:$9.79万
-
财政年份:1995
-
负责人:CHENG S LEE
-
依托单位:
海外基金