Detecting Individual Protein Conformation in Live Cells
Detecting Individual Protein Conformation in Live Cells
批准号:
7229810
负责人:
Keith R Weninger
金额:
$16.7万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-05-01 至 2009-08-31
关键词:
AreaBindingBiochemical ProcessBiologicalCatalytic DomainCell CommunicationCell physiologyCellsComplexCyclic AMP-Dependent Protein KinasesDevelopmentDiseaseDrug or chemical Tissue DistributionDyesEnergy TransferEukaryotic CellEventExhibitsExploratory/Developmental GrantFluorescenceFluorescence MicroscopyFluorescence Resonance Energy TransferFluorescent DyesGolgi ApparatusHealthHeterogeneityHomeostasisHumanIn VitroIndividualKnowledgeLabelLifeMammalian CellMeasurementMeasuresMembrane FusionMembrane Protein TrafficMethodsMicroinjectionsModelingMolecularMolecular ConformationPathway interactionsPhosphorylationPhosphotransferasesPhysiologicalProcessPropertyProtein ConformationProtein KinaseProteinsReactionReporterReportingResearchResolutionSNAP receptorSecond Messenger SystemsSignal TransductionSiteSpatial DistributionSpectrum AnalysisTechniquesTestingTimeTracerTransport ProcessTransport VesiclesVesicle Transport PathwayViruscellular targetingdesignimprovedin vivomembermutantparticlepathogenresearch studysecond messengersingle moleculesingle-molecule FRETsyntaxin
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This proposal aims to develop the new capability of using single molecule fluorescence (or Forster) resonance energy transfer (sm FRET) from proteins within living cells to observe real time conformational dynamics in parallel with spatial localization of individual proteins as they circulate within cellular networks. Experiments that follow single molecules can uncover properties that are impossible to observe in bulk measurements due to the inherent averaging over molecules and over time, and lack of synchronization. Single particle measurements of dynamic conformations of individual molecules can determine multiple reaction pathways and transient intermediate states as well as exact distributions of molecular properties. The general approach in this proposal is to use high resolution structural information already available for the proteins under study to design site-specific labeling mutants. These mutants will be produced, purified and labeled free of cells and then microinjected into cultured eukaryotic cells. Fluorescence microscopy and spectroscopy will be used to track individual protein molecules as well as determine the degree of FRET from that molecule in real time as they circulate within living cells. This untested approach, if successful, will have broad applicability to many biological questions and has the potential to reveal details of cellular networks that are not observable by any other technique. This approach will be applied within 2 different physiological networks to determine, 1) the spatial distribution and detailed sequence of folding/unfolding transitions in SNARE proteins involved in intracellular vesicle transport and membrane fusion, and 2) the activation of Protein Kinase A in second messenger signaling. Advances in understanding of cellular regulatory and signaling networks will have broad impact in all areas of health related research: understanding of the disease state, homeostasis and development. Ultimately knowledge derived with these methods will improve human health.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1038/nmeth.1421
发表时间:
2010-03
期刊:
NATURE METHODS
影响因子:
48
作者:
[Sakon, John J., Weninger, Keith R.]
通讯作者:
Weninger, Keith R.
Molecular mechanisms of DNA mismatch repair initiation
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批准号:10406898
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项目类别:
-
资助金额:$27.55万
-
财政年份:2019
-
负责人:Keith R Weninger
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依托单位:
Molecular mechanisms of DNA mismatch repair initiation
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批准号:10155520
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项目类别:
-
资助金额:$27.3万
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财政年份:2019
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负责人:Keith R Weninger
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依托单位:
Molecular Mechanisms of DNA Mismatch Repair Initiation
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批准号:10389275
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项目类别:
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资助金额:$8.1万
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财政年份:2019
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负责人:Keith R Weninger
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依托单位:
Detecting Individual Protein Conformation in Live Cells
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批准号:7010935
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项目类别:
-
资助金额:$19.92万
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财政年份:2006
-
负责人:Keith R Weninger
-
依托单位:
国内基金
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