grant

Core B: Macromolecular and Cellular Structure Core

Organization UNIVERSITY OF CALIFORNIA, SAN FRANCISCOLocation SAN FRANCISCO, UNITED STATESPosted 27 Sept 2021Deadline 31 Aug 2026
NIHUS FederalResearch GrantFY20252019 novel corona virus2019 novel coronavirus2019-nCoVAffectAffinityAirAssayAutoregulationBindingBioassayBiochemicalBiochemistryBiological AssayBiological ChemistryBody TissuesCOVID-19 virusCOVID19 virusCell BodyCell ComponentsCell StructureCellsCellular StructuresCellular biologyChaperoneChromatographyCoV-2CoV2ComplexCryo-electron MicroscopyCryo-electron tomographyCryoelectron MicroscopyDNA mutationDissociationElectron CryomicroscopyElectron MicroscopyEsteroproteasesFixativesGene AlterationGene MutationGene variantGeneticGenetic ChangeGenetic defectGenetic mutationGoalsHomeostasisHydrogen OxideIn VitroIntermediary MetabolismLeannessLightLysosomesMT-bound tauMacromolecular StructureMammalian CellMetabolic ProcessesMetabolismMethodologyMethodsMolecularMolecular ChaperonesMolecular ConfigurationMolecular ConformationMolecular InteractionMolecular StereochemistryMolecular StructureMutationOrganellesOxidesPeptidasesPeptide HydrolasesPhotoradiationPhysiological HomeostasisProcessProtease GeneProteasesProteinasesProteinsProteolytic EnzymesResolutionSARS corona virus 2SARS-CO-V2SARS-COVID-2SARS-CoV-2SARS-CoV2SARS-associated corona virus 2SARS-associated coronavirus 2SARS-coronavirus-2SARS-related corona virus 2SARS-related coronavirus 2SARSCoV2SamplingSevere Acute Respiratory Coronavirus 2Severe Acute Respiratory Distress Syndrome CoV 2Severe Acute Respiratory Distress Syndrome Corona Virus 2Severe Acute Respiratory Distress Syndrome Coronavirus 2Severe Acute Respiratory Syndrome CoV 2Severe Acute Respiratory Syndrome-associated coronavirus 2Severe Acute Respiratory Syndrome-related coronavirus 2Severe acute respiratory syndrome associated corona virus 2Severe acute respiratory syndrome coronavirus 2Severe acute respiratory syndrome related corona virus 2StructureTechnologyTherapeutic InterventionThinnessTissuesWaterWuhan coronavirusabnormally aggregated tau proteinage associatedage correlatedage dependentage linkedage relatedage specificallelic variantcell behaviorcell biologycellular behaviorconformationconformationalconformational stateconformationallyconformationscoronavirus disease 2019 viruscoronavirus disease-19 viruscryo-EMcryo-EM tomographycryoEMcryoEM tomographycryoelectron tomographycryogenic electron microscopyelectron cryo-tomographyextracellularfilamentous tau inclusiongene defectgenetic variantgenome mutationgenomic variantgraphenehCoV19innovateinnovationinnovativeinsightinterestintervention therapymagnetic beadsmedia consumptionmedia usemicrotubule associated protein tau aggregationmicrotubule associated protein tau depositmicrotubule bound taumicrotubule-bound taumutant allelenCoV2new approachesnovelnovel approachesnovel strategiesnovel strategyoverexpressoverexpressionpaired helical filament of taupreservationprotein complexprotein expressionprotein structureprotein structuresproteins structurereconstitutereconstitutionresolutionsself-aggregate taustructural biologytautau PHFtau Proteinstau accumulationtau aggregatetau aggregationtau factortau fibrillizationtau filamenttau neurofibrillary tangletau oligomertau paired helical filamenttau polymerizationtau-tau interactionτ Proteinsτ aggregation
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Full Description

PROJECT SUMMARY
The primary objective of the Macromolecular and Cellular Structure Core is to provide cutting edge,

innovative platforms for structural characterization responsive to needs and discoveries of the U54 FTD Center

without Walls. The long-term goal of this FTD Center without Walls is to understand the overall metabolism of

tau, how it is stabilized by chaperones and cochaperones and how it is channeled for degradation by the

lysosome. This core will use the latest methodologies in cryoEM to determine atomic resolution cryoEM

structures of relevant proteins and protein complexes as defined in Projects 1, 2 and to provide a cellular

context for tau lysosomal degradation via cryoEM-Tomography. The high-resolution studies will be enabled via

the expression and in vitro reconstitution of critical protein-protein complexes and novel cryoEM grid

technologies developed by the Agard lab. Additionally, the core will use its biochemical expertise to quantify

the existence of tau seeds for the other parts of the Center via RTQuiC assays. Together, the contributions

from this Core will be significant as they will reveal fundamental mechanisms dictating tau turnover and provide

novel targets for potential therapeutic intervention.

Grant Number: 5U54NS123985-05
NIH Institute/Center: NIH

Principal Investigator: DAVID AGARD

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