Molecular aspects of copper binding to the prion protein
Molecular aspects of copper binding to the prion protein
批准号:
8248205
负责人:
GLENN L MILLHAUSER
金额:
$27.85万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-03-01 至 2015-03-31
关键词:
AffinityAge of OnsetAlzheimer&aposs DiseaseAmino Acid SequenceApoptosisApoptoticBehaviorBindingBirdsBovine Spongiform EncephalopathyBrainC-terminalCellular StressCellular StructuresChemistryCleaved cellComplexCopperCreutzfeldt-Jakob SyndromeDepositionDeteriorationDiseaseDissociationDominant-Negative MutationEnvironmentEventFundingGlycoproteinsGoatHealthHomeostasisHumanIn VitroInfectious AgentInheritedIonsIschemic-Hypoxic EncephalopathyKuruLaboratoriesLeadLengthLesionLinkMagnetic ResonanceMaintenanceMammalsMeasurementMembraneMetal Ion BindingMetalloproteinsMetalsMicronutrientsMolecularMolecular ConformationMutationN-terminalNeuraxisNeurodegenerative DisordersNeuronsParkinson DiseasePathologyPeptide Sequence DeterminationPhasePhysiologicalPlayPolysaccharidesPrPPrion DiseasesPrionsProcessProtein GlycosylationProteinsRecombinant ProteinsRegulationResearchRoleScrapieSheepSiteSpin LabelsStructureSurfaceTechnologyTertiary Protein StructureTestingThermodynamicsThinkingTissuesTraumatic Brain InjuryWorkZincage relateddesignextracellularglycosylationin vivomutantnervous system disorderneurochemistryneuroprotectionnovelpreventprogramsprotein misfoldingpublic health relevancerelating to nervous systemresearch studytheoriesunpublished worksuptake
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The objective of this research program is to elucidate, at the molecular level, the mechanism and function of copper and zinc binding in the prion protein (PrP) and the relationship of these interactions to neuron maintenance and neurological disease. A misfolded form of the prion protein (PrP) is responsible for a class of fatal neurodegenerative diseases termed the Transmissible Spongiform Encephalopathies (TSEs), which include mad cow disease and Creutzfeldt-Jakob disease in humans. PrP is a highly abundant, membrane-bound glycoprotein found in all mammals and avian species. Although originally recognized for its role in neurodegenerative disease, it is now clear that PrP is essential for sustaining neuron function and regulating apoptosis. PrP takes up both copper and zinc at sites are essential for PrP activity. Over the last funding period, the PI's laboratory characterized structural and thermodynamic features of these metal ion sites and also identified a remarkable link between certain mutations and onset age in inherited prion disease. The next funding period will build on these findings using both magnetic resonance and cellular studies with the following projects: 1) determine the structure of the full-length, copper or zinc occupied protein; 2) evaluate how metal ions influence in vivo cleavage, implicated in apoptosis regulation; and 3) examine how structure and cellular behavior is altered by mutations associated with inherited disease, and also by mutations that prevent disease. Moreover, project three will apply new synthetic strategies for investigating the role of protein glycosylation. It is anticipated that these studies will provide fundamental new concepts for understanding the role of both PrP and copper in basic neurochemistry, and strategies for treating neurodegenerative disease and brain trauma.
PUBLIC HEALTH RELEVANCE: This research is aimed at evaluating proteins of the central nervous system that regulate copper and other micronutrients. These proteins are essential for neuron health and understanding their behavior will lead to new strategies for treating neurodegenerative diseases, such as Alzheimer's, and treating brain trauma.
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会议论文
Discovering How Cu(II)/Zn(II) Uptake by the Prion Protein Controls Structure, Function and Neurotoxicity
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批准号:9914103
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项目类别:
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资助金额:$34.26万
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财政年份:2019
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负责人:GLENN L MILLHAUSER
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依托单位:
Discovering How Cu(II)/Zn(II) Uptake by the Prion Protein Controls Structure, Function and Neurotoxicity
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批准号:10396527
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资助金额:$34.26万
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财政年份:2019
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负责人:GLENN L MILLHAUSER
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Discovering How Cu(II)/Zn(II) Uptake by the Prion Protein Controls Structure, Function and Neurotoxicity
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批准号:10612778
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资助金额:$34.26万
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财政年份:2019
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负责人:GLENN L MILLHAUSER
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批准号:9309934
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资助金额:$45.11万
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财政年份:2017
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财政年份:2010
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批准号:7367908
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资助金额:$28.28万
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财政年份:2005
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依托单位:
Molecular Determinants of AGRP Function
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批准号:7230448
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资助金额:$25.42万
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财政年份:2003
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依托单位:
Molecular control of melanocortin receptor signaling
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批准号:7676549
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项目类别:
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资助金额:$33.32万
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财政年份:2003
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负责人:GLENN L MILLHAUSER
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Molecular Determinants of AGRP Function
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批准号:6889213
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项目类别:
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资助金额:$26.9万
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财政年份:2003
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负责人:GLENN L MILLHAUSER
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依托单位:
Molecular Determinants of AGRP Function
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批准号:7065653
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资助金额:$26.22万
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负责人:GLENN L MILLHAUSER
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Molecular control of melanocortin receptor signaling
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资助金额:$27.6万
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资助金额:$33.77万
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批准号:6746052
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资助金额:$26.94万
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负责人:GLENN L MILLHAUSER
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依托单位:
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批准号:7802846
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项目类别:
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资助金额:$32.77万
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财政年份:2003
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负责人:GLENN L MILLHAUSER
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依托单位:
Molecular control of melanocortin receptor signaling
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批准号:8068181
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项目类别:
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资助金额:$29.11万
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财政年份:2003
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负责人:GLENN L MILLHAUSER
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依托单位:
Molecular aspects of copper and zinc binding to the prion protein
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批准号:9280977
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项目类别:
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资助金额:$31.36万
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财政年份:2002
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负责人:GLENN L MILLHAUSER
-
依托单位:
Molecular aspects of copper and zinc binding to the prion protein
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批准号:9273881
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项目类别:
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资助金额:$10.0万
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财政年份:2002
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负责人:GLENN L MILLHAUSER
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依托单位:
Molecular Aspects of Copper Binding to the Prion Protein
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批准号:7661475
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项目类别:
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资助金额:$24.38万
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财政年份:2002
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负责人:GLENN L MILLHAUSER
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依托单位:
海外基金