Small molecule modulators of the two-pore-domain potassium channel, TREK-2
Small molecule modulators of the two-pore-domain potassium channel, TREK-2
批准号:
8326898
负责人:
David Aaron Jacobson
金额:
$3.9万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-03-20 至 2014-02-28
关键词:
Afferent NeuronsBiological AssayCell LineCell physiologyCellsCollectionDetectionDevelopmentDiabetes MellitusDinoprostElectrophysiology (science)FluorescenceFluoxetineFutureHormonesHumanIon ChannelIslet CellLeadLibrariesLipidsMolecularMolecular BankMolecular Mechanisms of ActionMutagenesisNervous system structureNeuroendocrine CellNeuronsNeurosecretory SystemsPainPancreasPerformancePharmacologyPhosphorylationPhysiologicalPhysiological ProcessesPotassiumPotassium ChannelProtocols documentationRegulationRoleRunningSolutionsSpecificityStimulusTestingTetracyclinesThalliumTherapeuticVariantbasechemical synthesiscohorthigh throughput screeninghuman tissueinhibitor/antagonistinward rectifier potassium channelnew therapeutic targetnovel therapeuticspotassium channel protein TREK-1responsesmall moleculesmall molecule librariestool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The overall objective of this study is to identify specific and potent modulators of the two-pore-domain potassium channel, TREK-2. TREK-2 channels are important regulators of cellular electrical excitability and serve diverse physiological roles. TREK-2 is expressed predominately in the nervous system and pancreas, with strong expression in DRG neurons and neuroendocrine cells. TREK-2 channel activity may, thus, regulate stimuli detection of sensory neurons and neuroendocrine hormone secretion. However, our understanding of the role(s) of TREK-2 in human tissues remains obscure due to a lack of specific and potent pharmacology. Therefore, this project will utilize a robust thallium (Tl+) based fluorescent assay in a high throughput screen (HTS) to identify small molecule modulators of the human TREK-2 channel. The assay will be performed on a tetracycline inducible TREK-2 cell line, which was selected for based on its performance in the Tl+ assay. The TREK-2 Tl+ assay was validated with primary screens of two small molecule libraries including the Spectrum Collection (~2000 molecules) and a bioactive lipid library (~1000 molecules), which identified a small cohort of molecular regulators of TREK-2. The primary screens were utilized to optimize the Tl+ assay for use with the TREK-2 cell line in a large HTS. Building on these preliminary studies, this proposal plans to perform a HTS on the human TREK-2 channel with the diverse small molecule library at the Johns Hopkins Ion Channel Center within the Molecular Libraries Probe Centers Network. This will be accomplished using 1. A Tl+ flux based HTS, which will be followed by 2. Secondary assays utilizing Tl+ flux as well as electrophysiology to support rapid hit-to-lead progression and finally 3. A battery of tests including biophysical analysis, mutagenesis and phosphorylation analysis together with Tl+ flux; these will determine the mechanism of action, specificity and potency of the small molecule regulators of TREK-2. Molecular regulators of TREK-2 identified in this HTS will be utilized to test the influence of TREK-2 channels on human islet cell electrical activity and hormone secretion.
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会议论文
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资助金额:$50.57万
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财政年份:2023
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依托单位:
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资助金额:$44.96万
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Molecular Mechanisms Regulating Pancreatic Delta Cell Function and Dysfunction
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资助金额:$3.04万
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财政年份:2019
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资助金额:$39.21万
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财政年份:2019
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2-Pore-Domain K+ Channels as Novel Targets for Modulating Islet Hormone Secretion
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资助金额:$1.65万
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财政年份:2013
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负责人:David Aaron Jacobson
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依托单位:
2-pore-domain K+ channels as novel targets for modulating islet hormone secretion
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批准号:9112994
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项目类别:
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资助金额:$35.8万
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财政年份:2013
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负责人:David Aaron Jacobson
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依托单位:
2-pore-domain K+ channels as novel targets for modulating islet hormone secretion
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批准号:8690839
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项目类别:
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资助金额:$34.15万
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财政年份:2013
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负责人:David Aaron Jacobson
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依托单位:
2-pore-domain K+ channels as novel targets for modulating islet hormone secretion
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批准号:8579232
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项目类别:
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资助金额:$33.95万
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财政年份:2013
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负责人:David Aaron Jacobson
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依托单位:
Small molecule modulators of the two-pore-domain potassium channel, TREK-2
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批准号:8446273
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项目类别:
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资助金额:$3.9万
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财政年份:2012
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负责人:David Aaron Jacobson
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依托单位:
Pancreatic beta-cell CAMKII signaling under physiological and diabetic conditions
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批准号:8356456
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项目类别:
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资助金额:$7.8万
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财政年份:2012
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负责人:David Aaron Jacobson
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依托单位:
Pancreatic beta-cell CAMKII signaling under physiological and diabetic conditions
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批准号:8479356
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项目类别:
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资助金额:$7.53万
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财政年份:2012
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负责人:David Aaron Jacobson
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依托单位:
Secretagogue Induced Mechanisms Regulating Islet Electrical Activity
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批准号:8213176
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项目类别:
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资助金额:$10.23万
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财政年份:2009
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负责人:David Aaron Jacobson
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依托单位:
Secretagogue Induced Mechanisms Regulating Islet Electrical Activity
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批准号:7778926
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项目类别:
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资助金额:$0.62万
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财政年份:2009
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负责人:David Aaron Jacobson
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依托单位:
Secretagogue Induced Mechanisms Regulating Islet Electrical Activity
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批准号:8225312
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项目类别:
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资助金额:$14.5万
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财政年份:2009
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负责人:David Aaron Jacobson
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依托单位:
Secretagogue Induced Mechanisms Regulating Islet Electrical Activity
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批准号:8259512
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项目类别:
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资助金额:$14.5万
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财政年份:2009
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负责人:David Aaron Jacobson
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依托单位:
Secretagogue induced mechanisms regulating islet electrical activity
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批准号:7660745
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项目类别:
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资助金额:$10.62万
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财政年份:2009
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负责人:David Aaron Jacobson
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依托单位:
PEDIATRIC GVHD - PHARMACOKINETICS & BIOAVAILABILITY OF IV METHYLPREDNISOLONE
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批准号:7604294
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项目类别:
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资助金额:$0.41万
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财政年份:2006
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负责人:David Aaron Jacobson
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依托单位:
PEDIATRIC GVHD - PHARMACOKINETICS & BIOAVAILABILITY OF IV METHYLPREDNISOLONE
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项目类别:
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资助金额:$0.21万
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财政年份:2005
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负责人:David Aaron Jacobson
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依托单位:
海外基金