grant

Hydrogen Bonding Cavity Motifs About Metal Ions

Organization UNIVERSITY OF CALIFORNIA-IRVINELocation IRVINE, UNITED STATESPosted 1 Apr 1994Deadline 31 Dec 2026
NIHUS FederalResearch GrantFY2025Active SitesAgingAlkenesAmidesAminesAnimalsArchitectureAreaAwardAzacyclopropanesAziridinesBindingBiologicalBiologyCatalysisCharacteristicsChemicalsChemistryComplexCoupledDataDimethyleneiminesDioxygenDysfunctionElectronsEngineering / ArchitectureEnvironmentEthyleneiminesEthylenimineEthylenimine CompoundEvaluationExhibitsFunctional disorderFutureGoalsH-bondHealthHumanHydrogen BondingHydrogen OxideIndividualInvestigationIonsKineticsLibrariesLigand BindingLigandsLinkLiteratureMagnetismMaintenanceMediatingMetalloproteinsMetalsModern ManModificationMolecularMolecular InteractionNegative Beta ParticleNegatronsOlefinsOxidantsOxidation-ReductionOxidizing AgentsPathway interactionsPeptidesPhysiopathologyProcessProductionPropertyProteinsReactionRedoxReportingResearchRh (2,2'-biquinoline) complexRoleRouteSaturated AzacyclopropanesSiteStructureStructure-Activity RelationshipSystemTestingWateramineanalogbiologiccatalystchemical structure functioncis-(Rh(biq)2Cl2)Clcold temperaturecomplex Rdeprotonationdesigndesigningelectron acceptorexperimentexperimental researchexperimental studyexperimentsinsightlow temperaturemagneticmetalloenzymenitreneoxidationoxidation reduction reactionpathophysiologypathwaysocial rolestructural biologystructure function relationship
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Full Description

The broad purpose of the research in this proposal is to understand how microenvironrnents (secondary coordination
spheres) about metal ions control function. A bio-inspired synthetic approach is utilized that incorporates principles of

molecular architecture found in the active sites of metalloproteins into synthetic systems. Multidentate ligands will be

developed that create rigid organic structures around metal ions and place hydrogen bond donors or acceptors proximal

to the metal centers, forming specific microenvironments. One distinguishing attribute of these systems is the ability to

make site-specific modifications to the structure in order to evaluate correlations between the microenvironment and

reactivity. A focus of this research is the examination of transient intermediates that are formed from the activation of

dioxygen and the oxidation of water - processes that are directly linked to the maintenance of human health and aging.

Long-term goals include developing structure-function relationships in metal-assisted oxidative catalysis.

Metalloproteins perform functions not yet achieved in synthetic systems. Our hypothesis is that the lack of control of the

secondary coordination sphere in synthetic compounds is a major obstacle in establishing the desired functions. Results

from structural biology show that hydrogen bonds within the secondary coordination spheres of metalloproteins are

instrumental in regulating function. Therefore, the function and dysfunction of health-related metalloproteins can be

understood in the context of changes in their microenvironrnents. However, it is still unclear, even in biomolecules, how

non-covalent interactions influence metal-mediated processes. Investigations into these effects require fundamental

reactivity and mechanistic studies in which the contributions of single components can be analyzed individually. We

have developed synthetic hydrogen bonding systems in which the molecular components that define the structure

around the metal ion are specifically controlled; in turn, this permits the formation of systems whose activity can be

tailored to a particular function. This ability to regulate the microenvironment allows for systematic studies into structure-

function relationships that lead to fundamental understanding of chemical processes. Ultimately, this research will

provide insights into the properties of biological catalysts and lead to new classes of synthetic catalysts that exhibit the

exquisite control over reactivity that is characteristic of metalloenzymes.

Grant Number: 5R37GM050781-33
NIH Institute/Center: NIH

Principal Investigator: Andrew Borovik

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