Resource for Quantitative Elemental Mapping for the Life Sciences
Project Number5P41GM135018-04
Former Number5P41GM135018-02
Contact PI/Project LeaderO'HALLORAN, THOMAS V Other PIs
Awardee OrganizationMICHIGAN STATE UNIVERSITY
Description
Abstract Text
PROJECT SUMMARY – OVERALL
Inorganic chemistry plays myriad, evolutionarily-conserved roles in physiology and pathology. Cells must
accumulate several metals, such as zinc and iron, to millimolar levels in order to survive. They can deploy
fluctuations in metal content to control processes as varied as the mammalian cell cycle, pathogen infection
and neurological function. The critical regulatory role of metals is emphasized by the observation that one-third
of all protein-encoding genes in the human genome encode metal-dependent proteins. There is an increasing
appreciation in the NIH research community that intracellular content and subcellular location of each element
provides an inorganic signature that serves as a quantitative phenotype. These realizations are driving the
demand for new technologies for quantitative evaluation of inorganic signatures in cells and tissues. Such
methods are essential to understanding the regulation of physiological and pathogenic processes and
developmental decisions. The proposed Resource for Elemental Imaging for Life Sciences (QE-Map) will
develop and integrate emerging technologies to create transformative approaches to the compelling biological
question concerning inorganic chemistry in health and disease.
The technologies to be developed comprise a suite of three imaging and detection methods that will allow
investigators to quantitatively map the distribution of dozens of elements in samples ranging from cell extracts
to fixed cells to tissue slices. The complementary and integrative nature of these methods is critical to enabling
investigators to examine fluxes in intracellular ion content and localization, and to link these fluxes to changes
in distribution within tissues and in living animals. A multi-disciplinary team, located at Northwestern University
and Argonne National Laboratories, will address current limitations of LA-ICP-MS and SXFM technologies and
will launch the development of photoacoustic methods and probes to enable studies at the tissue level. We will
develop workflows and software that allows co-registration of images and standardization of quantitative data
that will maximize the impact and accelerate application to a broad range of biomedical research.
A portfolio of twelve DBPs was selected for their capacity to enable iterative development of new methods,
and address high impact research questions in the field of “inorganic physiology.” The DBPs focus on 4 themes:
(a) metal regulation in brain function and pathology; (b) metal modulation of host-pathogen interactions; (c)
metal fluxes controlling reproduction and development; and (d) metal imbalances in metabolic pathology.
A Community Engagement program will foster training of new technology users and dissemination of the
technologies to the scientific community. The integration and coordination of Resource projects and activities
will be enabled by the Administrative Core, co-directed by Drs. Thomas O’Halloran and Chris Jacobsen, and
supported by an External Advisory Committee and an Executive Committee.
Public Health Relevance Statement
NARRATIVE
The proposed Resource for Elemental Imaging for the Life Sciences (QE-Map) will advance and integrate new
and current technologies in an integrated workflow to create transformative approaches to the compelling
biological question of the role of metals, and other inorganic elements, in health and disease.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AccelerationAddressAdvisory CommitteesAffectAnimalsAutomobile DrivingBiologicalBiological MarkersBiological ProcessBiological SciencesBiologyBiomedical ResearchBrainCell CycleCell ExtractsCell physiologyCellsChemicalsChemistryCollaborationsCommunitiesComputer softwareCoordination and CollaborationCopperCore FacilityCountryDataDevelopmentDiagnosisDiseaseEcosystemElementsEmerging TechnologiesEngineeringFacultyFluorescence MicroscopyFosteringGenesGoalsGrowthHealthHumanHuman GenomeImageInductively Coupled Plasma Mass SpectrometryInfectionInfrastructureInorganic ChemistryIonsIronLaboratoriesLeadershipLifeLinkLocationMammalian CellMapsMetabolicMetabolic DiseasesMetabolismMetalsMethodsModelingNatureNerve DegenerationNervous System PhysiologyOrganismPathogenicityPathologicPathologyPhenotypePhotonsPhysicsPhysiologicalPhysiologyPlayPopulationPositioning AttributePreparationProcessProteinsQuantitative EvaluationsRegulationReproductionResearchResearch PersonnelResource AllocationResourcesRoentgen RaysRoleSamplingScanningScholars ProgramScienceSliceSourceStandardizationTechnologyTissuesTrainingTransition ElementsUnited States National Institutes of HealthUniversitiesWorkZincapplied biomedical researchcell fixingcommunity engagementdesigndetection methodfaculty researchfundamental researchimaging modalityindexingmeetingsmultidisciplinarynew technologypathogenphotoacoustic imagingprogramsrecruitresearch and developmentsingle cell technologytechnology developmenttechnology research and developmenttraining opportunityvisiting scholar
No Sub Projects information available for 5P41GM135018-04
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History
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