Toxic Metal Complexation by de Novo Designed Peptides
Project Number5R01ES012236-05
Contact PI/Project LeaderPECORARO, VINCENT L.
Awardee OrganizationUNIVERSITY OF MICHIGAN AT ANN ARBOR
Description
Abstract Text
DESCRIPTION (provided by applicant): Heavy metal poisoning by elements such as mercury, lead, cadmium, and arsenic is a significant human health problem. Understanding the interaction of heavy metals with proteins is essential for defining the mechanism of toxicity, developing ways to minimize human exposure and to provide therapeutic regimens for removal of toxic ions.
Our goals are (1) to develop peptide systems that provide a groundwork for the understanding of metalloregulatory proteins and metallochaperones, (2) to develop peptidic systems that can efficiently and selectively sequester heavy metal ions from aqueous solutions, and (3) to understand the thermodynamics and kinetics of metal binding to these designed peptides.
To achieve these goals we will use a de novo peptide system based on the three-stranded coiled coil peptide aggregate motif that encapsulates with high affinity single heavy metal ions and provides spectroscopic models of mercury, cadmium and arsenic binding sites in biological systems. We will generate high resolution structures of this peptide system in the presence and absence of these heavy metals, elucidate the kinetic and thermodynamic mechanisms of heavy metal encapsulation, and expand the array of characterized systems to transition metal ions Fe(II), Cu(I), Ni(II), Co(II) and Zn(II). We will also extend the original design to include single chain peptides that encapsulate heavy metals and coiled coils that provide different coordination environments than the original design and those that encapsulate more than one heavy metal ion.
These studies will expand the foundation of knowledge that has been laid by the scientific community investigating metallopeptide design, metalloregulatory proteins and heavy metal detoxification. These objectives will develop insight into the interplay between metal coordination and apopeptide structure in defining the overall metallopeptide fold, an important aspect of metallopeptide design. Also, development of highly efficient and specific heavy metal sequestering peptides could, ultimately, provide a viable and biodegradable means of removing heavy metals from contaminated water.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AchievementAdverse effectsAffinityArsenicBindingBinding SitesBiologicalBiological ModelsBiological ProcessBrain InjuriesCadmiumCellsCessation of lifeChloride IonChloridesCommunitiesConfusionCopperCoupledDevelopmentDrug Metabolic DetoxicationElementsEncapsulatedEngineeringEnvironmentEvaluationExcisionExposure toFoundationsGenerationsGoalsHeadacheHealthHeavy MetalsHumanInvestigationIonsKineticsKnowledgeLeadLesionLigandsLocationMercuryMetal Binding SiteMetalloproteinsMetalsModelingModificationNausea and VomitingNumbersObject AttachmentOrganismPeptidesPlacementProcessPropertyProteinsReactive Oxygen SpeciesResearchResearch PersonnelResolutionSeriesSiteSkinSolidSolutionsStructureSymptomsSystemTherapeuticThermodynamicsToxic effectTransition ElementsTreatment ProtocolsWateraqueousbasedesignexposed human populationgenetic regulatory proteinimprovedinsightmetal poisoningmetalloregulatory proteinnervous system disordernovelpeptide structurepolypeptidepreventprogramsprotein expressionresistance mechanismrespiratorytoxic metal
National Institute of Environmental Health Sciences
CFDA Code
113
DUNS Number
073133571
UEI
GNJ7BBP73WE9
Project Start Date
09-June-2003
Project End Date
31-March-2009
Budget Start Date
01-April-2007
Budget End Date
31-March-2009
Project Funding Information for 2007
Total Funding
$269,907
Direct Costs
$180,154
Indirect Costs
$89,753
Year
Funding IC
FY Total Cost by IC
2007
National Institute of Environmental Health Sciences
$269,907
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R01ES012236-05
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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Outcomes
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No Outcomes available for 5R01ES012236-05
Clinical Studies
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