Probing allosteric surfaces of NMDA receptors
Probing allosteric surfaces of NMDA receptors
批准号:
8460084
负责人:
Gabriela K Popescu
金额:
$32.25万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-07-01 至 2016-04-30
关键词:
AMPA ReceptorsAccountingAcuteAddressAffectAgonistAlzheimer&aposs DiseaseBindingBiochemistryBiologicalBiological ProcessBrainCellsCharacteristicsChronicClinicCysteineDiseaseElectrophysiology (science)EngineeringEvaluationEventFundingGlutamate ReceptorGlycineHomologous GeneHuntington DiseaseIndividualKineticsKnowledgeLigandsMeasurementMediatingModelingMotionMutagenesisMutationN-Methyl-D-Aspartate ReceptorsNerve DegenerationNeuropathyOutcomeOxidation-ReductionPainParkinson DiseasePathologyPatternPharmaceutical PreparationsPharmacologic SubstancePhysiologicalPhysiologyPlayPositioning AttributeProcessProteinsProtonsReactionReagentReceptor ActivationRelative (related person)ResolutionRoleSequence HomologySignal TransductionSiteStatistical ModelsStructural ModelsStructureSurfaceSynapsesTestingTherapeutic InterventionTherapeutic UsesTimeTweensWestern BlottingWorkZincacute strokeaddictionchronic strokecrosslinkdesensitizationdesigndimerextracellularflexibilityfunctional outcomesifenprodilinterfacialnervous system disorderneuropathologyneuroregulationneurotransmissionreceptorreceptor functionrelease of sequestered calcium ion into cytoplasmresearch studyresponsesimulationsingle moleculesuccesstherapeutic targettransmission process
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Numerous endogenous and synthetic ligands modulate NMDA receptor activities and are potential candidates for therapeutic intervention in a number of neurologic disorders. To date, empirical attempts to control en masse NMDA receptor-mediated fluxes have had only modest success in the clinic, mainly due to inadequate understanding of the mechanisms governing the allosteric control of NMDA receptor activities and of the specific roles played by these activities in brain physiology and pathology. Over the previous funding period the objective has been to delineate the mechanisms by which endogenous modulators (protons, zinc/ifenprodil, glycine) affect NMDA receptor gating dynamics and thus control the macroscopic response relevant to synaptic signaling. Over the next funding period the objective is to delineate the intracellular protein motions that constitute the NMDA receptor activation. The general approach is to capitalize on the recently solved atomic-resolution structure for a GluA2 tetrameric receptor, a NMDA receptor homologue and our growing expertise on NMDA receptor gating modulation. We will introduce mutations to perturb (increase and decrease) the relative mobility of NMDA receptor structural modules and will delineate the accompanying changes in reaction mechanism by kinetic analyses of single-molecule signals. Further, we will explore the time course of macroscopic responses obtained from receptors with restricted or enhanced internal motions to better understand how specific structural features support the unique biological functions played by NMDA receptors in brain physiology and pathology. Overall this work will provide critical information about structural correlates of NMDA receptor activation and will integrate the currently isolated structural and kinetic models of gating. Given that glutamate receptors mediate more than 90% of excitatory transmission in brain and NMDA receptors are critical to many fundamental brain functions, knowledge generated by the proposed experiments is likely to have wide impact on the fields of neurotransmission and neuromodulation.
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会议论文
Molecular Physiology of NMDA Receptors
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批准号:10665371
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项目类别:
-
资助金额:$52.44万
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财政年份:2023
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负责人:Gabriela K Popescu
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依托单位:
Activity of Minimal NMDA Receptors
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批准号:10743773
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项目类别:
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资助金额:$3.74万
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财政年份:2023
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负责人:Gabriela K Popescu
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依托单位:
Gating Mechanism of NMDA Receptors
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批准号:10413208
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项目类别:
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资助金额:$34.79万
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财政年份:2019
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负责人:Gabriela K Popescu
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依托单位:
Mechanical Activation of NMDA Receptors
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批准号:9329498
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项目类别:
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资助金额:$23.93万
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财政年份:2016
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负责人:Gabriela K Popescu
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依托单位:
NMDA receptors with restricted mobility of the ligand binding domain
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批准号:7578882
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项目类别:
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资助金额:$7.93万
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财政年份:2008
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负责人:Gabriela K Popescu
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依托单位:
NMDA receptors with restricted mobility of the ligand binding domain
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批准号:7450118
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项目类别:
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资助金额:$7.93万
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财政年份:2008
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负责人:Gabriela K Popescu
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依托单位:
NANOSCALE FLUCTUATIONS OF ERYTHROCYTE SUBDOMAINS IMAGED BY FOURIER PHASE MICROS
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批准号:7600894
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项目类别:
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资助金额:$4.69万
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财政年份:2007
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负责人:Gabriela K Popescu
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依托单位:
HILBERT PHASE MICROSCOPY OF RED BLOOD CELLS AFFECTED BY ALCOHOLISM
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批准号:7600898
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项目类别:
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资助金额:$2.34万
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财政年份:2007
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负责人:Gabriela K Popescu
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依托单位:
IMPROVED PERFORMANCE OF 4-PI MICROSCOPY USING HILBERT PHASE MICROSCOPY
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批准号:7600910
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项目类别:
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资助金额:$1.17万
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财政年份:2007
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负责人:Gabriela K Popescu
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依托单位:
HILBERT PHASE MICROSCOPY FOR INVESTIGATION OF RAPID DYNAMICS IN BIOLOGICAL SYST
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批准号:7600895
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项目类别:
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资助金额:$3.52万
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财政年份:2007
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负责人:Gabriela K Popescu
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依托单位:
FOURIER PHASE MICROSCOPY OF SICKLE CELL ANEMIA
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批准号:7600897
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项目类别:
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资助金额:$2.34万
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财政年份:2007
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负责人:Gabriela K Popescu
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依托单位:
MEASUREMENT OF CELL DRY MASS USING HILBERT PHASE MICROSCOPY
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批准号:7600911
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项目类别:
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资助金额:$1.17万
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财政年份:2007
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负责人:Gabriela K Popescu
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依托单位:
NON-CONTACT CHARACTERIZATION OF RED BLOOD CELL MECHANICAL PROPERTIES
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批准号:7600896
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项目类别:
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资助金额:$4.69万
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财政年份:2007
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负责人:Gabriela K Popescu
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依托单位:
MEMBRANE DYNAMICS OF RED BLOOD CELLS INFECTED BY P FALCIPARUM
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批准号:7600912
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项目类别:
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资助金额:$1.17万
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财政年份:2007
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负责人:Gabriela K Popescu
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依托单位:
Probing allosteric surfaces of NMDA receptors
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批准号:8651949
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项目类别:
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资助金额:$33.08万
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财政年份:2006
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负责人:Gabriela K Popescu
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依托单位:
Allosteric control of NMDA receptors
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批准号:7418625
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项目类别:
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资助金额:$33.18万
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财政年份:2006
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负责人:Gabriela K Popescu
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依托单位:
Allosteric control of NMDA receptors
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批准号:7799021
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项目类别:
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资助金额:$33.05万
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财政年份:2006
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负责人:Gabriela K Popescu
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依托单位:
HILBERT PHASE MICROSCOPY OF RED BLOOD CELLS AFFECTED BY ALCOHOLISM
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批准号:7357952
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项目类别:
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资助金额:$2.03万
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财政年份:2006
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负责人:Gabriela K Popescu
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依托单位:
NON-CONTACT CHARACTERIZATION OF RED BLOOD CELL MECHANICAL PROPERTIES
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批准号:7357950
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项目类别:
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资助金额:$4.07万
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财政年份:2006
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负责人:Gabriela K Popescu
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依托单位:
Probing allosteric surfaces of NMDA receptors
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批准号:8269874
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项目类别:
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资助金额:$33.42万
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财政年份:2006
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负责人:Gabriela K Popescu
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依托单位:
海外基金