Engineering of membrane protein chemosensors for therapeutic research
Engineering of membrane protein chemosensors for therapeutic research
批准号:
8453926
负责人:
JOSEPH Benjamin RUCKER
金额:
$50.87万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-07-01 至 2016-05-31
关键词:
AffectAgonistAlanineAmino Acid SubstitutionAmino AcidsAntibodiesBinding SitesBiological ProcessCell membraneCell surfaceCellsComplementComplexCrystallizationCrystallographyDetectionDevelopmentDietDrug Binding SiteDrug DesignEngineeringEnvironmental IrritantsEsthesiaExhibitsFDA approvedFamily memberG-Protein-Coupled ReceptorsGlucose TransporterGoalsHealthHumanIndividualIon ChannelIon Channel ProteinLibrariesLigandsMapsMembrane ProteinsMetabolic ControlMetabolic DiseasesModelingMolecularMolecular ConformationMutagenesisMutateMutationNutrientPainPharmaceutical PreparationsPharmacologic SubstancePhasePlasmidsPositioning AttributeProcessProtein EngineeringProtein FamilyProteinsPublicationsScanningShotgunsSignal TransductionSolutionsStimulusStructureSurfaceTRPV1 geneTaste PerceptionTechnologyTestingTherapeuticTherapeutic Human ExperimentationTimeVariantbasecancer paincommercial applicationinhibitor/antagonistmutantnovelpreferenceprotein functionprotein structurepublic health relevancereceptorsmall moleculetooltraffickingtransmission process
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Cells require the ability to detect and respond to stimuli in their surroundings, including to endogenous metabolites, exogenous nutrients, and environmental irritants. The proteins that are responsible for this process are called chemosensors and are involved in regulating diverse biological processes involved in pain sensation, dietary preference, and metabolic control. Because chemosensors transmit external environmental information into the cell, nearly all chemosensors are structurally-complex membrane proteins that span the cell's plasma membrane multiple times, such as ion channels, transporters, and G protein-coupled receptors. However, because most chemosensors are difficult to express, purify, and solubilize, structural and functional information about them has been exceptionally difficult to obtain. The goal of this Phase 2 proposal is to engineer chemosensors with increased surface expression and increased stability in solution and to map ligand and drug binding sites on these chemosensors.
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