课题基金 / 基金详情

Project 2

Project 2
项目2
批准号:
8692908
负责人:
Andras Fiser
金额:
$84.44万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
已结题
起止时间:
至 2015-08-31
关键词:
AddressAlgorithmsArchivesAreaAutomobile DrivingBiochemistryBioinformaticsBiologicalBiologyBiotechnologyCaliforniaCaringCell LineCell membraneCellular biologyChargeCommitCommunicable DiseasesCommunitiesComplexCoupledCryoelectron MicroscopyCrystallizationData CollectionDatabasesDepositionDevelopmentDiseaseEnsureEnzymesEukaryotic CellEvolutionFamilyFutureGenerationsGeneticHealthHomology ModelingHumanHuman ResourcesHybridsIllinoisImmuneIndividualInformaticsInformation DisseminationInsectaLabelLaboratoriesLeadershipLettersLightLinkMalignant NeoplasmsManualsMedicalMedicineMembrane ProteinsMethodsModelingModificationMolecularNMR SpectroscopyNational Institute of General Medical SciencesNeoplasm MetastasisNew YorkNew York CityNuclear PorePathogenesisPharmaceutical PreparationsPhotonsPlayPrincipal InvestigatorProcessProductionProgram Research Project GrantsProtein Structure InitiativeProteinsProtocols documentationRecordsRelianceResearchResearch InfrastructureResearch PersonnelResolutionRoboticsRoentgen RaysRoleRunningSan FranciscoSeleniumServicesSesame - dietaryShapesSignal PathwaySolutionsSourceSpecimenSpeedStructural ModelsStructureSupervisionSystemTechnologyTertiary Protein StructureTimeTriageUnited States National Institutes of HealthUniversitiesWashingtonWorkWritingbasebeamlinecollegecombatdata managementdesignexperienceextracellularflexibilityinsightknowledge basemacromoleculemedical schoolsmeetingsmembermetropolitannanomachinenovel strategiespathogenprogramsprotein complexprotein expressionprotein structurerepositoryrestraintscreeningstructural biologysuccesstechnology developmenttherapeutic developmenttumoruser-friendlyward

项目摘要

项目成果

Andras Fiser的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
The NYSGRC has a 10-year proven track record in high-throughput structure determination as well as in discovering and innplementing infrastructure to increase the speed, accuracy, success rate and affordability of structural biology studies. Moving forward the NYSGRC will reorganize to meet the new and diverse challenges associated with the PSI:Biology Network. In addition to reliance on traditional high-throughput bacterial expression platforms, the NYSGRC will develop and implement cutting-edge experimental and computational technologies to examine the biologically important molecules that are the focus of PShBiology. These targets are likely to include multidomain eukaryotic proteins, multi-component assemblies, and secreted proteins that underly complex multi-cellular biology and directly contribute to human health and disease. In addition to servicing the High-Throughput-Enabled Structural Biology Partnerships, this infrastructure will support our Biological Theme that focuses on the secretion machinery and secreted effector proteins from major bacterial, protozoan and fungal pathogens. These targets were specifically selected to provide new insights into the mechanisms that these pathogens have evolved for immune evasion and modulation of host signaling pathways. These processes rely on intricate nanomachines, with cytoplasmic, membrane-associated and extracellular components, that require hybrid computational and experimental approaches to define their organization, structure and function. Finally, our integrated experimental and computational efforts have identified new opportunities to significantly and economically enhance sequence/structure coverage. The advent of PShBiology is driving a process of evolutionary change for the NYSGRC that has already enhanced its outstanding high-throughput structure determination pipeline. Our stengths in traditional bacterial expression, coupled with novel approaches to eukaryotic expression and refolding, as well as our established expertise in hybrid methods, postions us to uniquely support the efforts of PShBiology.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Molecular basis of recognition in the Immunological Synapse
Molecular basis of recognition in the Immunological Synapse
Interdisciplinary protein engineering approach to design high affinity antibodies for flaviviruses
Interdisciplinary protein engineering approach to design high affinity antibodies for flaviviruses
海外基金