Development of high-throughput, high-sensitivity EPR sample handling capabilities for biomedical research
Development of high-throughput, high-sensitivity EPR sample handling capabilities for biomedical research
批准号:
10530690
负责人:
CANDICE S KLUG
金额:
$37.19万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-01-01 至 2024-11-30
关键词:
AreaAutomobile DrivingBiologicalBiological ModelsBiologyBiomedical ResearchBiomedical TechnologyCollectionCommunitiesComplexData CollectionDevelopmentDiseaseDrug DesignElectromagnetic FieldsElectron Spin Resonance SpectroscopyElectronsEngineeringEnvironmentEnzymesEquipmentFrequenciesGeometryGoalsInterventionKineticsMagnetismMeasurementMembraneMetalloproteinsMuramidaseOxidation-ReductionPerformancePositioning AttributeProtein ConformationProtein DynamicsReactionResearchSample SizeSamplingScienceSignal TransductionStructureSystemTechniquesTechnologyTemperatureTestingTimeTubebiophysical techniquesclinical diagnosticsdata acquisitiondesigndrug discoveryimprovedinnovationinstrumentinstrumentationmagnetic fieldmillisecondnanonew technologynovelprotein structureprototypesimulationstructural biologytheories
中文摘要
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英文摘要
Project Summary/Abstract
Electron paramagnetic resonance (EPR) spectroscopy is a critically important technique in biomedical research
with a unique ability to detect naturally occurring or engineered unpaired electrons in complex biological
environments. EPR has wide-ranging applicability to structural biology, metalloprotein research, redox biology,
rational drug design, and clinical diagnostics. Groundbreaking advancements in sample volume requirements
for biomedical EPR spectroscopy applications were made nearly four decades ago with the development of the
loop-gap resonator (LGR), which represented breakthrough benefits such as 10-fold lower sample volume
requirements and higher resonator efficiencies to increase signals over the commonly used cavity resonator. To
accommodate the biomedical needs of even further increased signal intensity and to provide the broader
scientific community with accessible technology, we propose to capitalize on our recent development of the
dielectric LGR (dLGR) concept and optimize this resonator technology to increase sensitivity beyond that
achieved upon introduction of the LGR. A dLGR is effectively a small dielectric resonator placed inside the inner
loop of an LGR where the return flux of the dielectric flows through the outer loops of the LGR. Analytic theory
and our high-frequency structure simulations indicate that the dLGR enables an order-of-magnitude
improvement in sensitivity over the LGR. To take full advantage of the extremely low volume requirements for
the dLGR, we propose to develop efficient sample handling technologies that couple the dLGR to high-
throughput sample handling instrumentation. We aim to develop two transformative technologies for biomedical
EPR applications: i) a nano-dLGR with a 10-fold increase in sensitivity for ~0.2 µL sample volumes integrated
with a customized autosampler and ii) a micro-dLGR for a dramatic increase in sensitivity for ~2 µL sample
volumes with an optimized stopped-flow system for millisecond time scale kinetics measurements. These
transformative and innovative prototypes with outstanding sensitivity will be easy to use and ultimately widely
available to the scientific community. Where the LGR was a transformative advance compared with cavity
resonators, the dLGR is expected to be another transformative leap from an LGR.
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Administrative Supplement to Development of high-throughput, high-sensitivity EPR sample handling capabilities for biomedical research
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批准号:10796325
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项目类别:
-
资助金额:$25.0万
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财政年份:2021
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负责人:CANDICE S KLUG
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依托单位:
Development of high-throughput, high-sensitivity EPR sample handling capabilities for biomedical research
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批准号:10323039
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项目类别:
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资助金额:$37.19万
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财政年份:2021
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负责人:CANDICE S KLUG
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依托单位:
Lpt protein-mediated transport of LPS
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批准号:10016341
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项目类别:
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资助金额:$35.42万
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财政年份:2014
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负责人:CANDICE S KLUG
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依托单位:
LptA-mediated transport of LPS
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批准号:9068198
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项目类别:
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资助金额:$29.07万
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财政年份:2014
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负责人:CANDICE S KLUG
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依托单位:
LptA-mediated transport of LPS
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批准号:8919418
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项目类别:
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资助金额:$29.07万
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财政年份:2014
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负责人:CANDICE S KLUG
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依托单位:
Lpt protein-mediated transport of LPS
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批准号:10205081
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项目类别:
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资助金额:$35.42万
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财政年份:2014
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负责人:CANDICE S KLUG
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依托单位:
Lpt protein-mediated transport of LPS
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批准号:9816218
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项目类别:
-
资助金额:$35.42万
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财政年份:2014
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负责人:CANDICE S KLUG
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依托单位:
LptA-mediated transport of LPS
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批准号:9275484
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项目类别:
-
资助金额:$29.07万
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财政年份:2014
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负责人:CANDICE S KLUG
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依托单位:
Lpt protein-mediated transport of LPS
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批准号:10440398
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项目类别:
-
资助金额:$35.42万
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财政年份:2014
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负责人:CANDICE S KLUG
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依托单位:
LptA-mediated transport of LPS
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批准号:8756571
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项目类别:
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资助金额:$29.07万
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财政年份:2014
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负责人:CANDICE S KLUG
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依托单位:
Acquisition of Q-band Pulsed EPR Capability
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批准号:8245467
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项目类别:
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资助金额:$38.09万
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财政年份:2012
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负责人:CANDICE S KLUG
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依托单位:
Acquisition of a Bruker E580 Pulse EPR Spectrometer
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批准号:7210413
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项目类别:
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资助金额:$50.0万
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财政年份:2007
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负责人:CANDICE S KLUG
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依托单位:
Site-directed spin labeling of ArnT
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批准号:7189855
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项目类别:
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资助金额:$21.33万
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财政年份:2004
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负责人:CANDICE S KLUG
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依托单位:
Site-directed spin labeling of ArnT
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批准号:6711998
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项目类别:
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资助金额:$24.6万
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财政年份:2004
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负责人:CANDICE S KLUG
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依托单位:
Spin Labeling of MsbA
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批准号:7656028
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项目类别:
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资助金额:$26.09万
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财政年份:2004
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负责人:CANDICE S KLUG
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依托单位:
Site-directed spin labeling of ArnT
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批准号:7384458
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项目类别:
-
资助金额:$20.93万
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财政年份:2004
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负责人:CANDICE S KLUG
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依托单位:
Spin labeling of MsbA
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批准号:7056046
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项目类别:
-
资助金额:$21.97万
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财政年份:2004
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负责人:CANDICE S KLUG
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依托单位:
Site-directed spin labeling of ArnT
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批准号:6868210
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项目类别:
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资助金额:$22.5万
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财政年份:2004
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负责人:CANDICE S KLUG
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依托单位:
Spin labeling of MsbA
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批准号:6877100
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项目类别:
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资助金额:$22.5万
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财政年份:2004
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负责人:CANDICE S KLUG
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依托单位:
Spin labeling of MsbA
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批准号:7227431
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项目类别:
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资助金额:$21.33万
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财政年份:2004
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负责人:CANDICE S KLUG
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依托单位:
海外基金