Subcellular Localization of Neuronal Ion Channels
Subcellular Localization of Neuronal Ion Channels
批准号:
7446663
负责人:
DONALD B ARNOLD
金额:
$28.49万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-06-01 至 2010-06-30
关键词:
Adaptor Signaling ProteinAddressAlzheimer&aposs DiseaseAmino Acid SequenceAmino AcidsAntibodiesApicalAtaxiaAxonBindingBrainC-terminalCell membraneCellsCerebellumChimeric ProteinsConditionDendritesDiseaseDisruptionDominant-Negative MutationEngineeringEpilepsyFamilyGelGenerationsGenus MenthaGoalsGrantHippocampus (Brain)Huntington DiseaseIn VitroIndiumIndividualIntegral Membrane ProteinIntracellular TransportIon ChannelKinesinKv4 channelLeadLearningLinkLocalizedMass Spectrum AnalysisMediatingMemoryMethodsModelingMolecularMonitorMotorN-terminalNeuronsPatternPeptide Signal SequencesPhage DisplayPhysiologicalPlayPotassium ChannelProcessPropertyProtein BindingProtein IsoformsProtein OverexpressionProteinsPurkinje CellsPurposePyramidal CellsRegulationResearchResearch PersonnelRoleSeriesSignal TransductionSilver StainingSliceSpatial DistributionSpecific qualifier valueStudy modelsTestingTimeTo specifyTransfectionVesicleVoltage-Gated Potassium ChannelWorkcell typefollow-uphippocampal pyramidal neuronin vivointracellular protein transportnervous system disorderneuronal cell bodyneuronal excitabilityprogramsprotein distributionprotein transportresearch studytooltrafficking
中文摘要
描述(由申请人提供):本基金提出的研究目的是从分子角度了解神经元中特定亚细胞区域离子通道定位的机制。研究将集中于阐明来自Kv4和Kv1家族的电压门控K+通道定位于神经元亚细胞区室的机制。其目的如下:1。探讨Kv1.3在小脑浦肯野细胞树突定位的机制。2. 目的:明确接头蛋白在Kv4.2转运和表达调控中的作用。3. 利用噬菌体展示抗体研究Kv4.2在皮层和海马锥体细胞树突状腔内定位的机制。4. 鉴定与Kv4.2二亮氨酸基序相互作用并在介导树突靶向通道中发挥作用的蛋白。本研究的最终目标是了解K+通道如何定位于神经元的特定亚细胞区域。这是K+通道调节的一个重要方面,其紊乱已被证明可导致癫痫等疾病。K+通道定位也将作为一种模型来理解蛋白质的亚细胞运输。蛋白质的亚细胞运输是神经元许多基本功能的基础,如学习和记忆。此外,错误的蛋白质运输与阿尔茨海默氏病和亨廷顿氏病等神经系统疾病有关。
英文摘要
DESCRIPTION (provided by applicant): The purpose of the studies proposed in this grant is to understand, in molecular terms, the mechanisms underlying the localization of ion channels to specific subcellular regions in neurons. Studies will concentrate on elucidating the mechanisms by which the voltage-gated K+ channels from the Kv4 and Kv1 families are localized to and within subcellular compartments in neurons. The aims are as follows: 1. To investigate the mechanisms underlying dendritic localization of Kv1.3 in Purkinje cells of the cerebellum. 2. To define the role of adaptor proteins in the transport and regulation of expression of Kv4.2. 3. To use phage display antibodies to investigate the mechanisms underlying localization of Kv4.2 within the dendritic compartment of cortical and hippocampal pyramidal cells. 4. To identify proteins that interact with the dileucine motif of Kv4.2 and play a role in mediating dendritic targeting of the channel. The ultimate goal of this research is to understand how K+ channels are localized to specific subcellular regions in neurons. This is an important aspect of K+ channel regulation, derangements of which have been shown to lead to diseases such as epilepsy. K+ channel localization will also serve as a model to understand subcellular trafficking of proteins in general. Subcellular trafficking of proteins underlies many essential functions of neurons, such as learning and memory. In addition faulty protein trafficking has been linked to such neurological diseases as Alzheimer's disease and Huntington's disease.
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海外基金