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Single-Molecule Studies of Synaptic Vesicles

Single-Molecule Studies of Synaptic Vesicles
突触小泡的单分子研究
批准号:
7504654
负责人:
Daniel T Chiu
金额:
$30.12万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-01 至 2012-06-30
关键词:
3-phosphoglycerateATP Synthesis PathwayAddressAffectAmphetaminesAntibodiesAntiepileptic AgentsAutomobile DrivingBackBindingBinding SitesBiochemicalBiogenesisBiological ModelsCaliberCalibrationCarrier ProteinsCategoriesCellsChromosome PairingCisplatin/Doxorubicin/Melphalan/TeniposideClassComplexConditionCountCoupledCouplingCrowdingDepthDiffusionDimensionsDisruptionElectron MicroscopyEndocytosisEndosome ProtonEnvironmentEnzymesEukaryotic CellEventExhibitsExocytosisExpenditureExtravasationFloorFluorescenceFluorescence MicroscopyFluorescent Antibody TechniqueGelGlassGlutamate TransporterGlutamatesGlyceraldehyde 3-PhosphateGreen Fluorescent ProteinsHandHypoglycemiaIndividualIntakeIntegral Membrane ProteinInvestigationKeppraKineticsKnowledgeLabelLasersLearningLengthLevetiracetamLipid BilayersLipidsLocationLysosome ProtonMacromolecular ComplexesMapsMeasurementMeasuresMembraneMembrane FusionMembrane Protein TrafficMembrane ProteinsMicroscopeModelingModificationMolecularMolecular NeurobiologyMonitorMotionMovementNatureNeurologicNeuronsNeurotransmittersNicotinamide adenine dinucleotideNigericinNumbersOregonOrganellesOxidoreductasePathway interactionsPeripheralPersonal SatisfactionPharmaceutical PreparationsPhosphoglycerate KinasePhysiologyPlayPositioning AttributePresynaptic TerminalsProceduresProcessProtein IsoformsProtein SortingsProteinsProteomicsProton PumpProton-Translocating ATPasesPumpRateRecyclingRelative (related person)ReportingResearchReserpineResolutionRibosomesRoleRole playing therapyRose BengalRotationRunningSNAP receptorSamplingSignal TransductionSiteSolutionsSorting - Cell MovementSpatial DistributionStagingStudy SectionSurfaceSynapsesSynaptic CleftSynaptic ReceptorsSynaptic TransmissionSynaptic VesiclesSynaptic plasticitySynaptophysinSystemTechniquesTestingThickThinkingTimeTransgenic MiceTransmembrane DomainTrypan BlueValinomycinVesicleViscosityWaterWorkbasecarbohydrate transportdimerdriving forcegamma-Aminobutyric Acidhuman VAPA proteininhibitor/antagonistinorganic phosphateinsightinterestmonoaminenervous system disorderneurotransmissionneurotransmitter releaseneurotransmitter uptakenumb proteinpH gradientpostsynapticpresynapticpreventprotein functionrab GTP-Binding Proteinsreceptorresearch studyresponsesensorsingle moleculesizesmall moleculestatisticsstoichiometrysynaptic functionsynaptogyrinsynaptotagmintraffickinguptakevesicle-associated membrane protein

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DESCRIPTION (provided by applicant): Gaining detailed knowledge on the workings of the vesicular transmitter uptake machinery is important in understanding synaptic function and plasticity, because this uptake process governs directly the number of transmitters released into the synaptic cleft and thus the degree of activation of the postsynaptic receptors. Determining the mechanism and rates of vesicular transmitter uptake also is important towards understanding the kinetics of vesicle recycling at the synapse and the energy requirements for loading and maintaining the filled vesicle at the presynaptic terminal. Given synaptic transmission is dependent on the uptake and storage of neurotransmitters within vesicles, it is not surprising that they are sites of action for many drugs, and thus understanding the functioning of this important molecular machinery will also have important pharmacological implications. Our proposed single-molecule and single-vesicle experiments are targeted towards deciphering the molecular organization and mechanism by which neurotransmitters are loaded into the synaptic vesicle. Towards this end, our specific aims are: Aim 1: Rotational measurements of synaptic vesicle integral membrane proteins and of small molecules contained within the vesicle Aim 2: Single-molecule studies of the vesicular H+ATPase Aim 3: Single-molecule studies of the vesicular glutamate transporters Aim 4: Investigation of the coupling of transmitter uptake to the glycolytic enzymes on synaptic vesicles and the spatial organization of the uptake machinery. From these experiments, we will develop an in-depth understanding of the workings of this complex molecular machinery with single-molecule resolutions, and offer new insight into how malfunctioning caused by neurological diseases or targeted disruption of this machinery with drugs can affect synaptic transmission. Project Narrative: To orchestrate neurotransmission, more than one thousand proteins are present at the presynaptic terminal and which either directly or indirectly interact with the synaptic vesicle, with the end result being the regulated release of neurotransmitters into the synaptic cleft. This high degree of convergence of presynaptic functions onto the synaptic vesicle has led to a "vesicocentric" view of neurotransmission that focuses on the synaptic vesicle as the central organelle in synaptic function. This proposal describes plans to study the synaptic vesicle with single-molecule resolutions, because discerning the detailed workings of this important organelle is critical in achieving the next level of quantitative understanding of synaptic transmission and malfunctioning caused by neurological diseases.
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会议论文
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  • 项目类别:
  • 资助金额:
    $226.78万
  • 财政年份:
    2023
  • 负责人:
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  • 依托单位:
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  • 批准号:
    10064842
  • 项目类别:
  • 资助金额:
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  • 财政年份:
    2020
  • 负责人:
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  • 依托单位:
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  • 批准号:
    10242940
  • 项目类别:
  • 资助金额:
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  • 财政年份:
    2020
  • 负责人:
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  • 依托单位: