grant

Virion, nucleocapsid, and inclusion body structures of Lloviu and Ebola viruses

Organization BOSTON UNIVERSITY MEDICAL CAMPUSLocation BOSTON, UNITED STATESPosted 11 Sept 2025Deadline 31 May 2027
NIHUS FederalResearch GrantFY20253-D3-D structure3-Dimensional3-dimensional structure3D3D structureArchitectureBatsBinding SitesBioinformaticsBiologyBostonCell BodyCell Surface GlycoproteinsCellsCellular InclusionsChiropteraCombining SiteCommunity HealthCryo-electron MicroscopyCryoelectron MicroscopyCytoplasmDangerousnessDataDiameterDiseaseDisorderEBOVEbola virusEbola-like VirusesElectron CryomicroscopyElectronsEngineering / ArchitectureFamilyFiloviridaeFiloviridae InfectionsFilovirusFrankfurt-Marburg Syndrome VirusFreeze SubstitutionFreezingGene TranscriptionGenerationsGenetic TranscriptionGenomeGlycoproteinsHumanHungaryIn Situ HybridizationInclusion BodiesItalyKnowledgeLabelLaboratoriesLengthLocationMacromolecular StructureMarburgMarburg virusMarburg-like VirusesMarburgvirusMembrane GlycoproteinsMessenger RNAMicroscopicMicrotomyModelingModern ManMolecular StructureMorphologyNatureNegative Beta ParticleNegatronsNucleocapsidOrthoebolavirusOrthomarburgvirusPathogenicityPhylogenetic AnalysisPhylogeneticsPropertyProtein Binding DomainProtein Binding MotifProtein-Protein Interaction DomainRNA ExpressionReactive SiteResearchResolutionSafetySamplingScientistShapesSiteStructureSurfaceSurface GlycoproteinsThickThicknessThin SectioningTranscriptionUniversitiesViralViral Gene ProductsViral Gene ProteinsViral Hemorrhagic FeversViral Inclusion BodiesViral ProteinsVirionVirusVirus AssemblyVirus ParticleVirus ReplicationWorkcommunity-based healthcomparativecryo-EMcryoEMcryogenic electron microscopycryogenicselectron tomographyexperiencefilovirus infectionsgenomic RNAglobal healthhemorrhagic feverhuman pathogenin situ Hybridization Geneticsin situ Hybridization Staining MethodinhibitorinsightmRNAnew drug targetnew druggable targetnew pharmacotherapy targetnew therapeutic targetnew therapy targetnovelnovel drug targetnovel druggable targetnovel pharmacotherapy targetnovel therapeutic targetnovel therapy targetpathogenpressureprotein structureprotein structuresproteins structureresolutionssmall molecular inhibitorsmall moleculesmall molecule inhibitorspatial and temporalspatial temporalspatiotemporalstructural biologythree dimensionalthree dimensional structuretomographyviral RNAviral assemblyviral multiplicationviral replicationvirologyvirus RNAvirus multiplicationvirus protein
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Full Description

Virion, nucleocapsid, and inclusion body structures of Lloviu and Ebola viruses
Structural diversity of filovirus virions and in particular nucleocapsids has been observed between Ebola virus

(EBOV) and Marburg virus (MARV). Lloviu virus (LLOV), a newly discovered filovirus, sits phylogenetically

between EBOV and MARV, providing a rare opportunity to expand our knowledge of the biology of this

dangerous family of pathogens.

Our team of virology, structural biology, and bioinformatics scientists proposes to determine the morphology of

LLOV virions using cryogenic electron microscopy and tomography (cryo-EM, cryo-ET), and compare the

structures of its nucleocapsid and its surface glycoproteins to those of EBOV and MARV. In addition, our

proposed studies will provide insights into the replication of LLOV and EBOV by determining three-dimensional

structures of viral replication factories (also called ‘inclusion bodies’) in infected human cells using thick sections

(~160 nm) of high pressure frozen/freeze-substituted samples for tomography. Thin sections (~50 nm) will be

analyzed using immunolabeling of viral proteins and RNA in-situ hybridization to localize sites of viral

transcription, genome replication, and nucleocapsid assembly.

Our studies will generate three-dimensional structures of LLOV virions, including structures of isolated viral

nucleocapsids. Macromolecular structures of virus nucleocapsids and virions can provide critical data with

regards to protein-protein interaction domains that could serve as the targets of small molecule inhibitors. In

addition, electron tomography will provide novel insights into the spatio-temporal morphology of viral replication

factories within LLOV- and EBOV-infected cells. In the proposed studies we will combine our unique expertise

in handling BSL-4 pathogens with our deep experience in structural biology to generate foundational knowledge

with respect to filovirus replication.

Grant Number: 1R21AI188100-01A1
NIH Institute/Center: NIH

Principal Investigator: ESTHER BULLITT

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