Bioenergetics Core
Bioenergetics Core
批准号:
9341347
负责人:
Craig Cano Beeson
金额:
$18.69万
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:
未结题
起止时间:
至
关键词:
Amino AcidsBicarbonatesBioenergeticsBiological AssayBiological ModelsBiological SciencesBiologyCarbon DioxideCardiacCell LineCell physiologyCellsCellular biologyCenters of Research ExcellenceComplexCore FacilityCouplingDNADataDevelopmentDiseaseDisease modelDoctor of PhilosophyElectronsEmbryoEnergy MetabolismEngineeringEquilibriumEquus caballusFailureFatty AcidsFluorescent ProbesGasesGeneticGenus HippocampusGlycolysisGoalsGoldHeadHeartHeart ValvesHeterogeneityHybridsHydration statusImageImage AnalysisImpairmentInterventionKidneyLactic acidLeadLiverMeasurementMeasuresMembrane PotentialsMetabolicMethodsMitochondriaMusNeuronsNutrientOrganellesOxidantsOxidation-ReductionOxidative StressOxygen ConsumptionPathologicPathway interactionsPeptidesPharmacologyPhasePhosphorylationPhysiologyPlayProductionProtonsReactionReactive Oxygen SpeciesRegulationRenal tubule structureResearch PersonnelResearch SupportResourcesRespirationRoleRunningSample SizeSamplingScienceServicesSignal TransductionSiteSliceSodium ChlorideSourceSouth CarolinaStreamStressStructureSystemTechniquesTechnologyTimeTissue SampleTissuesTranslationsValidationWorkZebrafishanaerobic glycolysisbasecell immortalizationcostdesigndrug discoveryestablished cell lineexperimental studyextracellulargene therapyimprovedin vivoinnovationinstrumentmetabolomicsmitochondrial membranemonolayeroxidationplanetary Atmosphereprofessorprogramsprotein functionsensorsuccesssugarsynergismtechnology validationtherapeutic targetthree dimensional cell culturetime usetooltumor
中文摘要
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英文摘要
CORE C: Bioenergetics Profiling Core
Director: Craig Cano Beeson, Ph.D.
Professor, Department of Drug Discovery and Biomedical Sciences
Project Summary
The primary goal of the Bioenergetics Profiling core facility is to support COBRE investigators in the
characterization of metabolite fluxes related to cellular redox and primary energy metabolism – the prevalent
sources of both the primary and secondary cellular redox species. The facility provides access to traditional,
`gold standard' techniques such as isotopomer, radiometric, and spectroscopic analyses. The core is also a
development site for the Seahorse Biosciences extracellular flux (XF) fluorometric technology used to measure
metabolic fluxes (i.e., oxygen consumption, CO2 and lactate extrusion) in real time using multiwell plates. The
basic Seahorse XF applications enable high throughput metabolic measurements with small sample sizes that
have transformed the utility of quantitative analyses of metabolic fluxes. Innovative adaptations of the XF
technologies developed in the core facility are providing access to real time flux measurements of redox
species in cells and tissues and, more importantly, the interrogation of bioenergetics pathways via use of
pharmacological or genetic interventions. We have coordinated these recent strategic technological
acquisitions into a core that provides analytical support for the efforts of the COBRE investigators and their
collaborators while also extending the technology to suit new efforts and further enable measurements with
improved translational potential. In the COBRE Phase I stage the core was known as the “Metabolomics Core”
that offered nascent Seahorse XF technology in addition to traditional single time-point quantification of
metabolite concentrations via LC-MS or NMR techniques. As described below, these traditional metabolomics
techniques were not as useful to the lead COBRE investigators as were the XF technologies, particularly as
the latter technology advanced and traditional metabolomics has matured. Because traditional metabolomics
analyses are now commercially available leading to cost reductions (much as academic DNA oligomer or
peptide cores became obsolete), the metabolomics core has been renamed as the “Bioenergetics Profiling
Core” to reflect the XF services we have developed that best support our investigators, and for which there are
no alternative external resources. Indeed, because XF technologies utilize living samples, it is unlikely they will
be easily `out-sourced'.
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资助金额:$80.74万
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财政年份:2010
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依托单位:
High Throughput Mitochondrial Nephrotoxicant Assay
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批准号:8001529
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资助金额:$26.93万
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财政年份:2010
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依托单位:
High Throughput Mitochondrial Nephrotoxicant Assay
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批准号:8334035
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财政年份:2009
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负责人:Craig Cano Beeson
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依托单位:
BINDING INTERACTIONS WITHIN PEPTIDE-MHC COMPLEXES
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项目类别:
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资助金额:$20.42万
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财政年份:2000
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BINDING INTERACTIONS WITHIN PEPTIDE-MHC COMPLEXES
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批准号:6127991
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资助金额:$22.42万
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财政年份:2000
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负责人:Craig Cano Beeson
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依托单位:
BINDING INTERACTIONS WITHIN PEPTIDE-MHC COMPLEXES
-
批准号:6690625
-
项目类别:
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资助金额:$9.25万
-
财政年份:2000
-
负责人:Craig Cano Beeson
-
依托单位:
BINDING INTERACTIONS WITHIN PEPTIDE-MHC COMPLEXES
-
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-
项目类别:
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-
财政年份:2000
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负责人:Craig Cano Beeson
-
依托单位:
Bioenergetics Core
-
批准号:9149872
-
项目类别:
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资助金额:$18.69万
-
财政年份:--
-
负责人:Craig Cano Beeson
-
依托单位:
海外基金