grant
Enzyme-Inspired Multimetallic Cooperativity: Leveraging Metal Pairing Effects for Heightened Reactivity
Organization UNIVERSITY OF MICHIGAN AT ANN ARBORLocation ANN ARBOR, UNITED STATESPosted 1 Sept 2025Deadline 31 Aug 2029
NIHUS FederalResearch GrantFY2025AcidsActive SitesActivities of Daily LivingActivities of everyday lifeAddressArchitectureBindingBiochemicalBiologic ModelsBiological FunctionBiological ModelsBiological ProcessBionomicsChemistryComplexDevelopmentDiamondE-MailEcologyElectronic MailElectronsElementsEmailEngineering / ArchitectureEnzyme GeneEnzymesEvolutionFe elementFeMo CofactorGeneHomologGoalsH-bondHealthHomologHomologous GeneHomologueHumanHydrogen BondingIonsIronIron-Molybdenum CofactorLifeMetalsMethodsMoFe ProteinModel SystemModelingModern ManMolecular InteractionMolybdenum-Iron ProteinMolybdoferredoxinMultienzyme ComplexesNegative Beta ParticleNegatronsO elementO2 elementOutcomeOxidantsOxidasesOxidation-ReductionOxidizing AgentsOxygenPharmaceutical AgentPharmaceuticalsPharmacologic SubstancePharmacological SubstancePreparationProcessPropertyProteinsRedoxResearchRoleSiteSpecificityStructureSystemTargeted ResearchTestingTherapeutic AgentsV elementVanadiumWorkadductcatalystdaily living functiondaily living functionalitydesigndesigningdevelopmentalelectron acceptorelectronic communicationelectronic structureenzyme complexfunctional abilityfunctional capacityinterestinterstitialmetallicitynitric oxide reductasenoveloxidation reduction reactionpharmaceuticalphotosystem IIpreparationssocial role
Description preview
Project Summary
Polynuclear mixed-metal active sites enact multielectron transformations central to global ecology. For example,
dinitrogen reduction, which is critical for enabling all of life’s biological processes, occurs at an iron-molybdenum
cofactor that proves markedly more efficient than its iron-vanadium homolog. Likewise, the oxygen…
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