Evolution of resistance to scorpion neurotoxins
Evolution of resistance to scorpion neurotoxins
批准号:
7386781
负责人:
ASHLEE Hedgecock ROWE
金额:
$5.04万
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:
2006-04-20 至 2009-04-19
关键词:
AffectAffinityAgitationAmino Acid SubstitutionAnimalsArizonaBindingBinding SitesBiological AssayBlurred visionCardiacCessation of lifeCodeConvulsionsDataEvolutionEye MovementsFamily memberFellowshipGated Ion ChannelGenesGenetic VariationGrasshoppersHabitatsHumanIndividualIon ChannelLimb structureMeasuresMembraneModificationMolecularMolecular GeneticsMusMuscleNamesNerveNeurotoxinsNumbersOrganismPainPatternPeripheral Nervous SystemPhysiologicalPopulationPotassium ChannelPredatory BehaviorProteinsPurposeResistanceRespiratory FailureRespiratory distressScorpion VenomsScorpionsSkeletal MuscleSodium ChannelSting InjuryTestingToxic effectToxicity TestsToxinVariantVenomsbasemutantneuromuscular systemresponsesaliva secretionspastic paralysisvoltage
中文摘要
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英文摘要
The Arizona bark scorpion (Centruroides exilicauda) and the striped bark scorpion (C. vittatus) produce
neurotoxins that selectively bind voltage-gated ion channels in excitable membranes of nerve and muscle,
producing hyper-excitability of the nervous and neuromuscular systems. Southern grasshopper mice
(Onychomys torridus) and Mearns' grasshopper mice (O. arenicola) are voracious predators of scorpions in
U.S. deserts. Southern and Mearns' grasshopper mice demonstrate physiological resistance to bark
scorpion venom. Variability in venom resistance among grasshopper mice populations co-varies with
geographic patterns of bark scorpion sympatry and allopatry. Electrophysiological assays show that ion
channels in the nerve and muscle of grasshopper mice are insensitive to scorpion neurotoxins. The purpose
of the proposed project is to determine the molecular genetic basis of ion channel insensitivity in resistant
mice, to characterize the molecular variation underlying phenotypic differences in resistance levels among
their populations, and to assess patterns of selection on genes involved in toxin resistance. Ion channel
encoding genes will be examined for structural and functional changes that impart insensitivity to toxins.
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会议论文
Structural basis of venom peptides that inhibit a Na+ channel regulator of pain
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批准号:10415506
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项目类别:
-
资助金额:$15.13万
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财政年份:2021
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负责人:ASHLEE Hedgecock ROWE
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依托单位:
Evolution of resistance to scorpion neurotoxins
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批准号:7230956
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项目类别:
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资助金额:$4.88万
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财政年份:2006
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负责人:ASHLEE Hedgecock ROWE
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依托单位:
Evolution of resistance to scorpion neurotoxins
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批准号:7114116
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项目类别:
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资助金额:$4.6万
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财政年份:2006
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负责人:ASHLEE Hedgecock ROWE
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依托单位:
海外基金