Guanidinium Toxins as Tools for Sodium Ion Channel Study
Guanidinium Toxins as Tools for Sodium Ion Channel Study
批准号:
7753181
负责人:
Justin Du Bois
金额:
$37.84万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-02-01 至 2012-01-31
关键词:
AcuteAffectBiological PhenomenaCellsChemical AgentsComplexDataDevelopmentElectricityHomology ModelingInflammationInvestigationIon Channel ProteinIonsKnowledgeLeadMapsMolecularMutagenesisNamesNerveNeuronsOral cavityPatternPharmaceutical PreparationsPoisonPreparationPrincipal InvestigatorProcessProtein IsoformsProteinsReagentResearchResearch DesignSaxitoxinSignal TransductionSiteSodium ChannelSourceStructureTetrodotoxinToxinchemical synthesischronic paindesignextracellulargonyautoxinsguanidiniuminjuredinterestmolecular sizenext generationpainful neuropathyprogramsprotein functionpublic health relevanceresearch studyresponsesmall moleculetooltransmission processvoltagezetekitoxin AB
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The overarching aim of this program is to develop small molecule tools for understanding ion channel protein function associated with the highly complex ionic mechanisms of electrical transmission in neuronal cells. Naturally occurring guanidinium poisons - tetrodotoxin, saxitoxin, gonyautoxin 2/3, and zetekitoxin AB - form the bedrock of these investigations. Despite evident differences in molecular size and topology, all four molecules are exquisitely potent blockers of voltage-gated sodium ion channels (NaV) that operate by occluding the extracellular mouth of the ion conductance pore (Site I). Studies of NaV structure, of which there exist ten mammalian isoforms, and function have been advanced with the availability from natural sources of tetrodotoxin, saxitoxin, and small number of structurally related forms. In the absence of crystallographic data, molecules such as gonyautoxin 2/3, zetekitoxin AB, and designed saxitoxin mimics in combination with protein mutagenesis experiments would enable current homology models of the channel pore to be challenged and refined. Knowledge accrued from these types of studies could lead to new chemical agents patterned after the guanidinium toxins that demonstrate NaV subtype specific activity. Such tools are desirable for mapping the spatial and temporal distribution of specific channel isoforms in developing or injured neurons. As NaV channels are considered lead actors in mechanisms for inflammation and neuropathic pain response, drugs that act on specific channel subtypes could represent next-generation therapies for the treatment of such ailments. PUBLIC HEALTH RELEVANCE: We are interested in understanding at a molecular level how nerve cells conduct electricity and how the process of electrical signaling is affected when a nerve is injured. Chemical synthesis is the engine that drives our program and will make possible the preparation of selective reagents that can be used to investigate these complex biological phenomena. Results from these studies could help guide the development of new therapies for the treatment of acute and/or chronic pain.
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财政年份:2016
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财政年份:2016
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依托单位:
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依托单位:
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依托单位:
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资助金额:$31.46万
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依托单位:
Reaction Design for the Synthesis of Neuroactive Agents
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批准号:6872152
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项目类别:
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资助金额:$31.4万
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依托单位:
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依托单位:
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依托单位:
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项目类别:
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依托单位:
海外基金