Electrophysiology-Optical Workstation for Ion Channel Biophysics
Electrophysiology-Optical Workstation for Ion Channel Biophysics
批准号:
7590799
负责人:
Sharona E Gordon
金额:
$49.94万
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:
2009-04-01 至 2011-03-31
关键词:
BiophysicsCalciumCell membraneCellsComplexDegradation PathwayDrug Delivery SystemsElectrophysiology (science)EventExplosionFundingGrowth FactorHealthHumanImageIon ChannelIon Channel ProteinIonsKnowledgeLifeMeasurementMediatingMethodologyMolecularMotionMovementMuscle CellsNervous System PhysiologyNervous system structureNeuronsOpticsPacific NorthwestPhosphatidylinositolsPhospholipidsPhosphoric Monoester HydrolasesPhosphorylationPhosphotransferasesPlayProteinsReadingRecyclingRequest for ProposalsRoleSecond Messenger SystemsSecretory CellSignal TransductionSignaling MoleculeSystemTimeTotal Internal Reflection FluorescentVascular SystemWorkcell typedesensitizationextracellularfluorescence imaginginstrumentnumb proteinorganelle movementpublic health relevancereceptorreceptor internalizationresidencesecond messengertraffickingtranscription factor
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): In the last two decades we have witnessed an explosion in knowledge of the normal and pathological function of the nervous system. Progress has been largely fueled by advances in two methodologies, fluorescence imaging and electrophysiology. We propose to begin the next wave of discovery, by combining optical and electrophysiological measurements of living cells, to probe their function in real time. The excitability of neurons, secretory cells, and muscle cells is influenced by a large number proteins and second messengers: transcription factors determine the number of ion channels and receptors that are produced; kinases, phosphatases, and ions determine the activity of channels and receptors; and complex recycling and degradation pathways determine the residence time of channels and receptors in the plasma membrane. As well, the phospholipids that compose the plasma membrane play an active role in determining channel activity and the rate of channel and receptor internalization. We will image the movement of proteins and signaling molecules within a cell with confocal and TIRF microscopy and read out the net effect of signaling on the cell's excitability using electrophysiological recording. This proposal requests funds for a Confocal-TIRF-Electrophysiological (CTE) workstation for ion channel biophysics. No such instrument exists in the Pacific Northwest. It would permit us to synchronize the movement of organelles, interactions between proteins, changes in intracellular calcium concentration, intra-molecular conformational changes, and electrical activity into a cohesive understanding of how cellular excitability is set, how it is perturbed by extracellular signals, and how it recovers after a signaling event. Using these methodologies, we will ask questions such as: Which calcium-activated signals regulate desensitization? What is the mechanism by which phosphoinositides regulate channels? How do growth factors regulate channel trafficking? How does phosphorylation regulate channel activity and expression? What are the molecular motions that underlie gating? These questions will be asked across a number of cell types, to define ion channel function quantitatively in several systems essential to human health. PUBLIC HEALTH RELEVANCE: Excitable cells depend on ion channel proteins to conduct electrical signals, regulate force, and mediate secretion. In fact, over half of all drug targets are ion channels or proteins that directly regulate ion channels. Our work is directed toward understanding the normal and pathological signaling by ion channels in the nervous system and vascular system.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Conformational Energetics and Heterogeneity to Reveal Gating Mechanisms of TRPV and TRPM Ion Channels
-
批准号:10793400
-
项目类别:
-
资助金额:$23.41万
-
财政年份:2022
-
负责人:Sharona E Gordon
-
依托单位:
Conformational Energetics and Heterogeneity to Reveal Gating Mechanisms of TRPV and TRPM Ion Channels
-
批准号:10627103
-
项目类别:
-
资助金额:$6.65万
-
财政年份:2022
-
负责人:Sharona E Gordon
-
依托单位:
Conformational Energetics and Heterogeneity to Reveal Gating Mechanisms of TRPV and TRPM Ion Channels
-
批准号:10590571
-
项目类别:
-
资助金额:$40.43万
-
财政年份:2022
-
负责人:Sharona E Gordon
-
依托单位:
Conformational Energetics and Heterogeneity to Reveal Gating Mechanisms of TRPV and TRPM Ion Channels
-
批准号:10404753
-
项目类别:
-
资助金额:$46.09万
-
财政年份:2022
-
负责人:Sharona E Gordon
-
依托单位:
Conformational Energetics and Heterogeneity to Reveal Gating Mechanisms of TRPV and TRPM Ion Channels
-
批准号:10752849
-
项目类别:
-
资助金额:$19.96万
-
财政年份:2022
-
负责人:Sharona E Gordon
-
依托单位:
Conformational Energetics and Heterogeneity to Reveal Gating Mechanisms of TRPV and TRPM Ion Channels
-
批准号:10728394
-
项目类别:
-
资助金额:$11.35万
-
财政年份:2022
-
负责人:Sharona E Gordon
-
依托单位:
Conformational Energetics and Heterogeneity to Reveal Gating Mechanisms of TRPV and TRPM Ion Channels
-
批准号:10605108
-
项目类别:
-
资助金额:$6.62万
-
财政年份:2022
-
负责人:Sharona E Gordon
-
依托单位:
Multimodal Gating Mechanisms of TRPV1 Ion Channels
-
批准号:10082453
-
项目类别:
-
资助金额:$41.99万
-
财政年份:2018
-
负责人:Sharona E Gordon
-
依托单位:
Mechanisms of TRPV1 Channel Regulation
-
批准号:8638032
-
项目类别:
-
资助金额:$40.54万
-
财政年份:2012
-
负责人:Sharona E Gordon
-
依托单位:
Mechanisms of TRPV1 Channel Regulation
-
批准号:8257782
-
项目类别:
-
资助金额:$29.35万
-
财政年份:2012
-
负责人:Sharona E Gordon
-
依托单位:
Mechanisms of TRPV1 Channel Regulation
-
批准号:8471730
-
项目类别:
-
资助金额:$28.33万
-
财政年份:2012
-
负责人:Sharona E Gordon
-
依托单位:
Mechanisms of TRPV1 Channel Regulation
-
批准号:8721105
-
项目类别:
-
资助金额:$7.45万
-
财政年份:2012
-
负责人:Sharona E Gordon
-
依托单位:
Inflammatory hyperalgesia due to TRPV1, the pepper spray receptor in the cornea
-
批准号:10475208
-
项目类别:
-
资助金额:$33.94万
-
财政年份:2006
-
负责人:Sharona E Gordon
-
依托单位:
Inflammatory hyperalgesia due to TRPV1, the pepper spray receptor in the cornea
-
批准号:10414845
-
项目类别:
-
资助金额:$10.66万
-
财政年份:2006
-
负责人:Sharona E Gordon
-
依托单位:
Inflammatory hyperalgesia mediated by TRPV1, the pepper spray receptor in cornea
-
批准号:7905402
-
项目类别:
-
资助金额:$56.03万
-
财政年份:2006
-
负责人:Sharona E Gordon
-
依托单位:
Inflammatory hyperalgesia due to TRPV1, the pepper spray receptor in the cornea
-
批准号:9982957
-
项目类别:
-
资助金额:$34.99万
-
财政年份:2006
-
负责人:Sharona E Gordon
-
依托单位:
Inflammatory hyperalgesia mediated by TRPV1, the pepper spray receptor in cornea
-
批准号:7487744
-
项目类别:
-
资助金额:$37.11万
-
财政年份:2006
-
负责人:Sharona E Gordon
-
依托单位:
Inflammatory hyperalgesia mediated by TRPV1, the pepper spray receptor in cornea
-
批准号:7129574
-
项目类别:
-
资助金额:$38.9万
-
财政年份:2006
-
负责人:Sharona E Gordon
-
依托单位:
Inflammatory hyperalgesia due to TRPV1, the pepper spray receptor in the cornea
-
批准号:8444824
-
项目类别:
-
资助金额:$34.76万
-
财政年份:2006
-
负责人:Sharona E Gordon
-
依托单位:
Inflammatory hyperalgesia due to TRPV1, the pepper spray receptor in the cornea
-
批准号:8657437
-
项目类别:
-
资助金额:$34.07万
-
财政年份:2006
-
负责人:Sharona E Gordon
-
依托单位:
国内基金
海外基金
Calcium/NFAT/GLUT3通路调控糖酵解代谢在CAR-T细胞耗竭中的作用和机制研究
-
批准号:--
-
项目类别:面上项目
-
资助金额:52万元
-
批准年份:2022
-
负责人:张明明
-
依托单位:
miR-30调控Calcium/Calcineurin通路在慢性肾脏病心肌保护中的作用
-
批准号:81670699
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2016
-
负责人:郑春霞
-
依托单位:
水稻OsCAS(Calcium-sensing Receptor)基因的功能分析
-
批准号:30900771
-
项目类别:青年科学基金项目
-
资助金额:20.0万元
-
批准年份:2009
-
负责人:赵昕
-
依托单位: