Dynamics of Clathrin Coat Formation in Cells
Dynamics of Clathrin Coat Formation in Cells
批准号:
8817882
负责人:
TOMAS KIRCHHAUSEN
金额:
$40.29万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-10 至 2018-12-31
关键词:
AffectAuxilinsBindingBiochemistryCapsid ProteinsCell CommunicationCell surfaceCellsCellular MembraneClathrinCoated vesicleCoupledDataDynaminEndocytosisEnvironmentEnzymesEpidermal Growth Factor ReceptorEpitheliumEventFunctional disorderGrantGrowthGrowth FactorGuanosine Triphosphate PhosphohydrolasesHormonesImageImageryImaging technologyLeadLifeLigandsLightLipid BilayersLipid BindingLipidsLow-Density LipoproteinsMediatingMembraneMembrane Protein TrafficMicroscopyMolecularOrganismPathway interactionsPatternPhosphatidylinositolsPhosphoric Monoester HydrolasesPhosphotransferasesPhysiologicalPhysiologyProcessProtein DynamicsProteinsRecruitment ActivityRegulationResearchResolutionRoleSUM-159 Breast Cancer Cell LineSignal TransductionSpecificitySpecimenStagingStructureSurfaceTFAP2A geneTestingTimeTissuesToxinTransferrinTransmembrane TransportVirusWorkZebrafishbasecoated pitconstrictiondetectorepsinfluorophoregenome editingin vivointersectin 1new technologypathogenpublic health relevancereceptorreceptor mediated endocytosisscaffoldsingle moleculetrafficking
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Reorganization of cellular membranes and transport of components from one lipid-bilayer bounded compartment to another underlie much of the internal structure of a cell. Clathrin is the principal molecular scaffold for a number of such processes -- most notably, receptor-mediated endocytosis of ligands such as transferrin, LDL, growth factors, and hormones. Viruses and other pathogens and pathogenic toxins usurp this pathway to enter cells. Direct observation of the biochemistry of clathrin-dependent membrane traffic in living cells is now possible, through a combination of genome editing and single-fluorophore sensitivity imaging. The combination, which amounts to in vivo, single-molecule biochemistry, resolves ambiguities about essential components and the time points at which they function, particularly when many of the steps have a stochastic rather than fully deterministic character. Our work in the previous grant period on the molecular mechanism of coated-pit initiation illustrates the value of single-fluorophore-sensitivity imaging approaches. I the research described in this proposal, we will analyze the molecular mechanisms of transitional checkpoints in coat assembly, develop and apply probes for the roles of specific phosphoinositide lipids in regulating clathrin- based membrane traffic, and extend our "imaging biochemistry" to the 3D context of multicellular assemblies and living tissues. We will capitalize on a transformative new imaging technology, lattice light- sheet microscopy (LLSM), which enables rapid, high-resolution, high-sensitivity 3D visualization of whole cells and multicellular specimens, including living tissues.
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财政年份:2008
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依托单位:
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依托单位: