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Drug Discovery and Structural Biology Core

Drug Discovery and Structural Biology Core
药物发现和结构生物学核心
批准号:
10059201
负责人:
John Charles Williams
金额:
$19.44万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-08-01 至 2022-11-30
关键词:
Advisory CommitteesAffinityAgreementAntibodiesBackBasic ScienceBindingBiochemicalBiomedical EngineeringBiopolymersCalorimetryCancer Center Support GrantCancer cell lineCellsChelating AgentsChemicalsCircular DichroismCitiesCity of Hope Comprehensive Cancer CenterClinical ResearchClinical TrialsComplexComputer AnalysisComputer softwareComputing MethodologiesCrystallizationCustomDNADevelopmentDigit structureDiseaseDyesEquipmentExclusionFacultyFeedbackFlowersFundingHouse StaffsHumanHybridsImageIncubatorsIndividualInsectaIon-Exchange Chromatography ProcedureLabelLeadLegal patentLibrariesLicensingLigandsLiquid substanceMalignant NeoplasmsMeasuresMethodsModelingMolecular MedicineNMR SpectroscopyNatural ProductsNucleosidesOligonucleotidesOrganic ChemistryOutcomePTPRC genePeer ReviewPeptidesPharmaceutical ChemistryPharmaceutical PreparationsProcessProductionPropertyProtein DynamicsProteinsPublicationsRNAResearchResearch InstituteResearch PersonnelResource SharingRobotRoboticsRoentgen RaysS PhaseServicesSiteSmall Interfering RNASolidSpecificityStructureStructure-Activity RelationshipSurface Plasmon ResonanceSurveysSystemTechnologyTherapeuticTherapeutic AgentsTitrationsTrainingTranslational ResearchValidationVisualizationWaterWorkanaloganalytical ultracentrifugationaptamerassay developmentbasebiophysical techniquescohesioncomputerized toolscost effectivedesigndrug discoverydrug structureexperienceexperimental studyfast protein liquid chromatographyhigh throughput screeningimprovedin silicoinsightinstrumentinstrumentationlead candidatemacromoleculemass spectrometermembermilligrammolecular dynamicsmutantnanonanoparticlenovelnovel therapeuticspharmacokinetics and pharmacodynamicspreclinical evaluationprofessorprogramsprotein protein interactionprotein structureresearch studyscreeningsimulationsmall moleculesmall molecule inhibitorstemstructural biologysugartherapeutic developmentvirtual

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英文摘要
Drug Discovery and Structural Biology Shared Resource ABSTRACT The Drug Discovery and Structural Biology (DDSB) Core collaborates with City of Hope investigators to validate, develop, and optimize novel therapeutics. To accomplish this, the DDSB provides a comprehensive range of services spanning computational methods; high throughput screening (HTS); advanced synthetic methods to produce small molecules, peptides, and challenging oligonucleotides; and structural and biophysical methods. These services provide City of Hope Comprehensive Cancer Center (COHCCC) members with a cohesive platform to rapidly and successfully drive their therapeutic development efforts to meaningful outcomes. All major equipment and instrumentation for the DDSB is located in the Flower building. This includes an extensive array of liquid handling robots; peptide and oligonucleotide synthesizers; multiple incubators and fast protein liquid chromatography (FPLC) systems for protein production and purification; analytical instrumentation to characterize molecular interactions (surface plasmon resonance [SPR], isothermal titration calorimetry [ITC], analytical ultracentrifugation, circular dichroism [CD] with thermal control, etc.); NMR and mass spectrometers for small molecules; and equipment for macromolecular determinations (crystallization and visualization robots and a diffractometer). The DDSB core is co-directed by Drs. David Horne and John Williams, Professors in the Department of Molecular Medicine at the Beckman Research Institute at City of Hope, and supported by highly qualified staff that maintain and operate the equipment while also providing training to COHCCC researchers who wish to operate instruments independently. Oversight is provided by an interdisciplinary faculty Advisory Committee, and user feedback through an annual survey. Since the last competitive renewal, the core contributed to 219 publications by CC members, served 121 unique investigators, 100 (83%) of whom were CC members and represent all five Programs. Of the 100 CC members, 86 had peer-reviewed funding. In addition, since the last competitive renewal, the DDSB has synthesized more than 300 small molecules, 500 peptides, and 950 oligonucleotides (aptamers, GpC-conjugates, etc.). During that same period, over 450 crystallization and optimization trials were conducted, over 250 crystals were screened for diffraction, over 40 novel crystal structures/complexes were determined, and over 300 SPR experiments, 35 in silico screening/molecular dynamics projects, and 23 HTS projects were conducted. The DDSB has also developed synthetic methods and processes leading to full-scale production of complex small molecules under GMP conditions. Efforts stemming from the DDSB have led to 32 technology/patent portfolios involving 76 patents (pending and allowed), four licenses, and a substantial sponsored research agreement (>$1M).
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RATIONAL DESIGN TO MODULATE ANTIBODY AFFINITY
  • 批准号:
    8362416
  • 项目类别:
  • 资助金额:
    $0.06万
  • 财政年份:
    2011
  • 负责人:
    John Charles Williams
  • 依托单位:
MICROWAVE SYNTHESIS OF ARYLPHOSPHONIUM SALTS BOUND TO FLUORESCENT MARKERS
  • 批准号:
    8360079
  • 项目类别:
  • 资助金额:
    $1.07万
  • 财政年份:
    2011
  • 负责人:
    John Charles Williams
  • 依托单位:
RATIONAL DESIGN TO MODULATE ANTIBODY AFFINITY
  • 批准号:
    8362351
  • 项目类别:
  • 资助金额:
    $0.14万
  • 财政年份:
    2011
  • 负责人:
    John Charles Williams
  • 依托单位:
RATIONAL DESIGN TO MODULATE ANTIBODY AFFINITY
  • 批准号:
    8170356
  • 项目类别:
  • 资助金额:
    $0.03万
  • 财政年份:
    2010
  • 负责人:
    John Charles Williams
  • 依托单位:
海外基金