Structure and function of ABC transporters to understand persistence of global ma
Structure and function of ABC transporters to understand persistence of global ma
批准号:
8389520
负责人:
GEOFFREY A CHANG
金额:
$17.47万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-24 至 2017-07-31
关键词:
ABCC1 geneATP HydrolysisATP phosphohydrolaseATP-Binding Cassette TransportersAnimalsAnisotropyAntisense OligonucleotidesBindingBiologicalBiological AssayBiological ModelsBiologyCarrier ProteinsCell LineCell physiologyCellsChemicalsComplementary DNACrystallizationDataEmbryoEmployee StrikesEnvironmentExposure toFamilyFishesFluorescenceFluorescence AnisotropyFundulus heteroclitusGeneticGoalsHealthHumanIn VitroIntegral Membrane ProteinLaboratoriesMarinesMeasuresMediatingMembrane ProteinsModelingMolecularMolecular StructureMulti-Drug ResistanceMusMusselsMytilusPatternPharmaceutical PreparationsPollutionPolychlorinated BiphenylsProteinsRecombinantsResearch InfrastructureResearch PersonnelResolutionSeaSea UrchinsSeafoodStructureSubstrate InteractionSystemToxic effectUnited States National Institutes of HealthXenobioticsYeastsZebrafishaquatic organismbasebioaccumulationcytotoxicitydrug efficacyembryo cellenvironmental chemicalexperienceexpression cloningin vitro Assayin vitro testingin vivoinhibitor/antagonistloss of functionmanmarine organismmolecular transportermulti drug transporterorganochlorine pesticidepollutantpollutant interactionprotein structurepublic health relevancetooluptake
中文摘要
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英文摘要
DESCRIPTION (provided by applicant)
Marine pollution is of concern for human health through our exposure to contaminated food from the sea. What remains poorly understood is why some chemicals are persistent, accumulating in marine organisms and then in humans, while others are not. Multidrug resistance (MDR) transporters, belonging to the ATP Binding Cassette (ABC) family, are major biological determinants of intracellular chemical accumulation. While they have been implicated as determinants of environmental chemical persistence and used as tools for predicting availability and efficacy of drugs, they have yet to be systematically applied to predicting persistence of pollutants. The investigators' preliminary data indicate striking functional conservation of the major sub-family types (ABCB, ABCC and ABCG) of xenobiotic eliminating transporters between sea urchins and man. This application explores the molecular basis for this conserved substrate selectivity as a first step towards application of transporter biology to prediction of pollutant persistence. In this project, the investigators will over-express, solubilize, and purify
sea urchin multidrug efflux transporter proteins, develop assays for their interaction with major marine pollutants and attempt to determine their high-resolution structures. They will measure their interaction with persistent marine pollutants using anisotropy, ATPase and whole cell assays. By comparing structure and functions of sea urchin with those of mammalian transporter proteins, already available through the TransportPDB pipeline, they will identify conserved residues and structural features that are essential for predicting substrate interaction in the poly-specific binding pocket of these ABC transporters
Public Health Relevance: Certain molecular transporters found in sea urchins and other marine organisms determine the uptake of persistent pollutants from the sea. The goal of this high-impact project is to provide a detailed molecular framework for understanding the structure and function of these important transporters. This application fulfills an important need to develop biologically-based tools to predict bioaccumulation and toxicity of marine pollutants as relevant to human health and environment.
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