Chemical mapping of protein networks that sense cellular force
Chemical mapping of protein networks that sense cellular force
批准号:
10385719
负责人:
Anna Katherine Koster
金额:
$6.76万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-04-05 至 2023-04-04
关键词:
AddressAgonistBindingBinding SitesBiologyBiotinylationBlood flowBreathingC-terminalCalibrationCandidate Disease GeneCell LineCell membraneCell modelCell physiologyCell surfaceCellsChemicalsCoupledCytoskeletonDataDevelopmentDiseaseElementsEnvironmentExtracellular MatrixExtracellular ProteinFellowshipGoalsHealthHorseradish PeroxidaseHumanIon ChannelJointsLaboratoriesLearningLightLungMapsMass Spectrum AnalysisMechanicsMediatingMembrane ProteinsMentorshipMethodsMolecularN-terminalNatureNervous system structureOrganPhysiologicalPhysiological ProcessesPhysiologyPiezo ion channelsPlayProcessProteinsProteomicsRNA InterferenceResearch InstituteResearch TrainingRoleSensorySignal TransductionSkinStretchingTechniquesTechnologyTestingTissuesTouch sensationTrainingTranslationsalpha Bungarotoxinbaseblood pressure regulationcancer cellcareer developmentcell motilitycell typedesignendothelial stem cellextracellularhigh throughput screeningimaging platforminnovationinsightknock-downmechanical forcemechanical signalmechanical stimulusmechanotransductionmeetingsnew technologynovelnovel strategiespressurepressure sensorprotein complexresponseshear stresssmall moleculestem cell differentiationsuccesstraining projecttransmission process
中文摘要
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英文摘要
Project Summary/Abstract
The body’s ability to sense and respond to mechanical forces, or mechanosensation, is critical to a variety
of physiological processes from macroscopic processes like regulation of blood pressure and breathing to small-
scale processes like cell migration, cell fate determination, and cell alignment during tissue development. Despite
the importance of mechanosensation in human heath, the details governing pressure sensing in different tissues
and organs remain unknown. Mechanosensitive ion channels called PIEZO channels that respond to stretching
or compression of the plasma membrane are now known to play an important role in mechanical signaling within
cells, but the ability of PIEZO channels to tune their response over a vast dynamic range of forces in different
cell types is still a mystery. Evidence points to the existence of distinct PIEZO interaction networks in different
cell types (e.g., attachments to the cytoskeleton, extracellular matrix, and/or interactions with other protein
auxiliary subunits) that enable calibration of PIEZO mechanotransduction. Reliable identification of such
interactions has faced significant obstacles due to gaps in technology for studying ion channels.
This proposal will aim to address these gaps by developing a new proteomic mass spectrometry-based
approach for mapping PIEZO protein networks that sense cellular force. Success of this project will provide
insight into many mechanically mediated processes that are poorly understood in human health and disease and
provide a generalizable new technique for defining of ion channel interaction networks on the cell surface. The
research training for this project will be conducted with joint mentorship in the Patapoutian and Cravatt labs at
the Scripps Research Institute, two well-equipped laboratories with expertise in ion channel physiology and
chemical biology/proteomic mass spectrometry, respectively. Regularly occurring joint meetings with the sponsor
and co-sponsor will provide an adequate training environment to learn new techniques and facilitate career
development goals for the duration of the fellowship.
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国内基金
海外基金
Agonist-GPR119-Gs复合物的结构生物学研究
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批准号:32000851
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项目类别:青年科学基金项目
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资助金额:24.0万元
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批准年份:2020
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负责人:乔安娜
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依托单位: