grant

New techniques for detecting and handling nanocrystals for cutting edge structural biology methods

Organization STATE UNIVERSITY OF NEW YORK AT BUFFALOLocation AMHERST, UNITED STATESPosted 17 Sept 2022Deadline 31 Aug 2026
NIHUS FederalResearch GrantFY20253-D structure3-dimensional structure3D structureAccelerationAcousticsAddressAlgorithmsBindingBiologicalBiological FunctionBiological ProcessBrightfield AnalysisBrightfield MicroscopyCausalityCharacteristicsClassificationCommunitiesComputational toolkitConventional X-RayCoupledCryo-electron MicroscopyCryoelectron MicroscopyCrystal DepositionCrystal FormationCrystallizationCrystallographiesCrystallographyDataDepositDepositionDetectionDevelopmentDiffusionDiseaseDisorderDrug DesignElectron CryomicroscopyEtiologyGeneralized GrowthGenerationsGrowthHealthHumanImageImage AnalysesImage AnalysisInvestigatorsKnowledgeLaboratoriesLifeLiquid substanceMacromolecular StructureMethodsMicroscopyModelingModern ManMolecularMolecular InteractionMolecular StructureMultimodal ImagingOpticsProcessPropertyProteinsResearchResearch PersonnelResearchersResolutionSamplingSingle Crystal DiffractionSolventsSourceStructural BiologistStructural ModelsStructureSynchrotronsSystemSystematicsTechniquesTechnologyTestingTherapeuticTimeTissue GrowthVisible LightVisible Light RadiationVisible RadiationVisualizationX Ray CrystallographiesX-Ray CrystallographyX-Ray Diffraction CrystallographyX-Ray ImagingX-Ray Medical ImagingX-Ray/Neutron CrystallographyXray CrystallographyXray imagingXray medical imagingbiologiccausationcomputational toolboxcomputational toolscomputational toolsetcomputerized toolsconventional Xraycryo-EMcryoEMcryogenic electron microscopydensitydesigndesigningdetection methoddetection proceduredetection techniquedevelopmentaldiffuseddiffusesdiffusingdiffusionsdisease causationelectron diffractionempowermentenzyme mechanismexperimentexperimental researchexperimental studyexperimentsfluidfrontierimage evaluationimage interpretationimage registrationimage-based methodimagingimaging methodimaging modalityimprovedinnovateinnovationinnovativeinnovative technologiesliquidmacromoleculemath methodologymath methodsmathematical approachmathematical methodologymathematical methodsmathematics approachmathematics methodologymathematics methodsmethod developmentmolecular targeted therapeuticsmolecular targeted therapiesmolecular targeted treatmentmulti-modal imagingmulti-modality imagingmultimodal data fusionmultimodal fusionmultimodality imagingnano litrenanocrystalnanoliternanolitrenew drug targetnew druggable targetnew pharmacotherapy targetnew therapeutic targetnew therapy targetnovelnovel drug targetnovel druggable targetnovel pharmacotherapy targetnovel therapeutic targetnovel therapy targetontogenyoptic imagingopticaloptical imagingparticlephysical propertyprotein data bankprotein databankresolutionsscreeningscreeningsskillsstructural biologysub micronsubmicrontech developmenttechnology developmentthree dimensional structuretool
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Full Description

Project Summary
Determining the detailed structural characteristics of biomolecules relevant to human health and disease

is one of the most crucial tools in our arsenal for understanding disease etiology and mechanism, and for

being able to develop new therapeutics that target these molecular entities. There are new techniques in

structural biology, including serial femtosecond crystallography, serial synchrotron crystallography, and

microcrystal electron diffraction, that have the potential to greatly advance structure determination of

biomolecules and to empower access to structural details that have defied characterization via other

structural methods. These new structural methods all rely on being able to generate, detect and

appropriately handle extremely small crystalline samples of biomolecules. This requirement for sub-

micron sized crystals is one of the key features of these technologies, and presents a major obstacle

to the advancement of these methods for structure determination. This proposal presents innovative

technologies for both image analysis and sample handling expressly designed to address the specific

challenges of working with submicron crystals. We plan to use nonlinear optical microscopy methods

coupled with purpose-built application of point process modeling and wavelet image analysis approaches

to provide computational tools needed to enable detection and characterization of submicron samples

that are invisible to the brightfield microscopy tools that are typically used in sample generation and

experimental set up for crystal based structural biology. In addition, we will examine different fixed target

platforms to reduce sample handling, minimizing potential crystal damage, as well as test use of acoustic

droplet ejection techniques for nanoliter volume sample transfer. These innovations will be a powerful

addition to structural biology toolbox for leveraging the cutting edge diffraction based methods currently

available for structure determination. These technology developments will break through key barriers to

the widespread use of these cutting edge structural methods.

Grant Number: 5R01GM141273-05
NIH Institute/Center: NIH

Principal Investigator: Sarah Bowman

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