Opsineering: Engineering Novel ChannelRhodospins for Optogenetics Applications
Opsineering: Engineering Novel ChannelRhodospins for Optogenetics Applications
批准号:
8963322
负责人:
Claire Nicole Bedbrook
金额:
$3.67万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-01 至 2017-08-31
关键词:
AddressAnimalsAutistic DisorderBiologicalBiological AssayBrainBrain regionCationsCellsCharacteristicsChemical StimulationChimera organismCollaborationsColorDevelopmentDiagnosisDrug abuseElectric StimulationElectrophysiology (science)EngineeringEvolutionFamilyFoundationsGated Ion ChannelGenetic RecombinationGoalsHomologous GeneIonsKineticsLaboratoriesLengthLibrariesLifeLightLiteratureMammalian CellMembraneMental DepressionMental disordersMethodsModelingMutateMutationNeurobiologyNeuronsNeurosciencesOpsinOrganismParkinson DiseasePathway interactionsPermeabilityPhotophobiaPopulation HeterogeneityProbabilityPropertyProtein EngineeringProteinsResearchResearch TrainingSchizophreniaSpecific qualifier valueSpecificitySpeedStimulusStructureSystemTechniquesTimeTransgenic OrganismsVariantWorkaddictionbasebrain circuitrycell typedesensitizationdesigndirected evolutionimprovedlight gatedmembermicrobialmillisecondmutantnervous system disorderneuronal circuitrynext generationnoveloptogeneticsprotein functionpublic health relevancescreeningsingle moleculesuccesstool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Optogenetics is genetically encoded, optically induced, control of cells through transgenic expression of microbial opsins in mammalian neurons. When these opsins are expressed in a cell-type specific manner and light activated, they provide temporally and spatially separated stimulation of independent hyperpolarizing and depolarizing channels in neurons in living animals. Channelrhodopsins (ChRs) are the microbial opsins used in optogenetics to trigger light induced depolarization. ChRs are light-gated ion channels that operate on the order of milliseconds, a time scale relevant for neuronal activation, and can be expressed in the membrane of distinct cell types with high temporal precision in well-defined brain regions. This contrasts with the poor temporal dynamics or lack of specificity of chemical or electrical stimulation methods. However, the optogenetics tools currently available for neuronal circuit interrogation are limited based on expression, light-wavelength activation, kinetics and ion specificity. Our proposed project addresses these limitations through protein engineering. Protein engineering through directed evolution and structure-guided recombination are well-established methods for modifying and optimizing proteins for desired functions. Current literature and preliminary collaborative work between the Gradinaru and Arnold labs at Caltech indicate that channelrhodopsins are amenable to functionally useful laboratory evolution and manipulation. This work will be focused toward engineering improved channelrhodopsins for use as biological tools in optogenetics. The aim is to engineer channelrhodopsins for optimal ion selectivity, kinetics, reversibility, and shifted light excitatio wavelengths. These new channel proteins will have applications in probing the brain's circuitry to better understand and model healthy and non-healthy brain function as a foundation for controlling and diagnosing neurological disorders such as addiction, depression and Parkinson's disease.
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Reprogramming organismal lifespan through modulation of neuropeptides
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批准号:10507323
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项目类别:
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资助金额:$12.85万
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财政年份:2023
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负责人:Claire Nicole Bedbrook
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依托单位:
Opsineering: Engineering Novel ChannelRhodospins for Optogenetics Applications
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批准号:9125904
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项目类别:
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资助金额:$3.72万
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财政年份:2014
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负责人:Claire Nicole Bedbrook
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依托单位:
海外基金