Analysis of the Yeast MRP Subfamily of ABC Transporters
Analysis of the Yeast MRP Subfamily of ABC Transporters
批准号:
7173736
负责人:
Christian M Paumi
金额:
$1.07万
依托单位:
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:
2005-12-01 至 2007-01-31
关键词:
ABCC1 geneATP phosphohydrolaseATP-Binding Cassette TransportersAddressArsenicArsenitesBindingBiologicalBiological AssayCadmiumCellsCellular StressChemicalsChronic Idiopathic JaundiceComplexCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorDiseaseDrug Metabolic DetoxicationEmployee StrikesFigs - dietaryGenesGeneticGlutathioneGuanine Nucleotide Exchange FactorsGuanosine TriphosphateGuanosine Triphosphate PhosphohydrolasesHeavy MetalsIn VitroLeadLeukotrienesMammalian CellMammalsMediatingMedicalMembraneMembrane ProteinsMercuryMetabolicMetabolic PathwayMethodsMolecular GeneticsMulti-Drug ResistanceMultidrug Resistance-Associated ProteinsMutagenesisMutationN-terminalNaturePH DomainPharmaceutical PreparationsPhenotypePhysiologicalPigmentsPlayPolymerase Chain ReactionProteinsPseudoxanthoma ElasticumQuality ControlRestRoleS100A12 geneSaccharomyces cerevisiaeSite-Directed MutagenesisStandards of Weights and MeasuresStress TestsSystemTestingTherapeuticToxic Environmental SubstancesToxinYeastsanalogbasechemical geneticsdesignhuman S100A12 proteinin vivoinfancyinsightinterestlead ionmembermutantnovelprotein transportresearch studytoolyeast geneticsyeast two hybrid system
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The multidrug resistance-associated protein (MRP) subfamily of the ATP-binding cassette (ABC) transporters plays a key role in protecting cells from drugs and environmental toxins such as heavy metals (mercury, arsenic, lead, and cadmium). The MRPs (also called ABCCs) are distinguished from other ABC transporters by two striking hallmarks: 1) they contain an additional "N-terminal extension" with a conserved region called L0, and 2) they transport substrates in the form of glutathione (GSH)-conjugates or complexes. Here, we will use the powerful genetic, molecular, and cellular tools available in Saccharomyces cerevisiae to address several key issues of the MRPs. Our specific aims are to: 1) determine whether conserved residues within the L0 of MRPs are specific for GSH binding; 2) assess whether novel interactors, recently identified for the yeast MRP Ycflp, play an integral role in the general mechanism of MRP transport; and 3) test the possibility that a major role of the MRP's is to dispose of potentially harmful "metabolic detritus", using genetic and chemical screens. Overall, our analysis may suggest more effective therapies for MRP- based diseases (e.g. DJS, PXE, cystic fibrosis) and/or aid in reducing damage from environmental toxins.
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NEGATIVE REGULATION OF THE YEAST MRP, YCF1P, AND THE HUMAN MRPS BY CK2
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批准号:8360576
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项目类别:
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资助金额:$24.99万
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财政年份:2011
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负责人:Christian M Paumi
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依托单位:
NEGATIVE REGULATION OF THE YEAST MRP, YCF1P, AND THE HUMAN MRPS BY CK2
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批准号:8168250
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项目类别:
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资助金额:$23.25万
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财政年份:2010
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负责人:Christian M Paumi
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依托单位:
NEGATIVE REGULATION OF THE YEAST MRP, YCF1P, AND THE HUMAN MRPS BY CK2
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批准号:7960501
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项目类别:
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资助金额:$19.42万
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财政年份:2009
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负责人:Christian M Paumi
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依托单位:
Analysis of the Yeast MRP Subfamily of ABC Transporters
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批准号:7057024
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项目类别:
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资助金额:$4.88万
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财政年份:2005
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负责人:Christian M Paumi
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依托单位: