Reductive Dehalogenation in Mammals by Iodotyrosine Deiodinase
Reductive Dehalogenation in Mammals by Iodotyrosine Deiodinase
批准号:
7698635
负责人:
STEVEN E ROKITA
金额:
$34.25万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-06-15 至 2013-04-30
关键词:
Active SitesAlanineAmino AcidsAnabolismBacteriaBindingBiologicalBiologyCatalysisChemistryCongenital AbnormalityCrystallizationDataDependenceDietDistantElectronsEnvironmentEnzymesEvolutionFamilyFlavinsFlavoproteinsFundingHealthHomeostasisHomologous GeneHormonesHumanHuman ActivitiesHydrogen BondingHydrolysisHypothyroidismInvestigationIodide PeroxidaseIodidesIodineLifeMammalsMeasuresMediatingMetabolicMetabolismMicrobeMono-SNADH oxidaseNADPOrganismOxidation-ReductionOxidoreductasePathway interactionsPersonal SatisfactionPositioning AttributeProcessPropertyProteinsPyrimidinePyrimidinesReactionRecruitment ActivityRecyclingRoleSelenocysteineStructureSubstrate InteractionSubstrate SpecificityTestingThyroid GlandThyroxineTimeTissuesTreesanalogbasecarboxyl radicalcofactordehalogenationdeiodinationdesigndietary requirementfascinatefunctional groupgazehormone biosynthesismutantnoveloxidationprogenitorpublic health relevanceresearch study
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Organohalides are ubiquitous in the environment through natural and human activities. Most organisms detoxify and degrade these compounds by enzyme-mediated hydrolysis, elimination or oxidation. Certain microbes are also capable of promoting reductive dehalogenation, although this is primarily limited to anaerobic metabolism. Mammals provide a fascinating exception to this general observation. The essential hormone, thyroxine (3-[4-[4-hydroxy-3,5-diiodophenoxy]-3,5-diiodophenyl]alanine), is reductively deiodinated in a variety of tissues by selenocysteine-containing enzymes. Quite surprisingly, an entirely different strategy has been recruited in the thyroid to deiodinate 3-iodo- and 3,5-diiodotyrosine. In this case, a unique flavoprotein, iodotyrosine deiodinase, is responsible for reducing the iodinated amino acids in order to salvage iodide for reuse in thyroxine biosynthesis. Investigations are now proposed to identify the unprecedented chemistry and mechanism of this mammalian deiodinase. The novel properties of this enzyme will extend the known repertoire of flavin-dependent catalysis and pathways available in biology to process halogenated compounds. Our description of catalysis will focus on the reduction of the C-I bond and concomitant oxidation of the reduced flavin in IYD. Spectroscopic and product analyses will be used to differentiate between one and two electron processes and, for the first time, reveal the full range of substrates that are processed by IYD. Activation of both the substrate and flavin cofactor will be described by independently measuring recognition and catalytic properties of enzyme mutants and substrate analogues. Concurrently, substrate-dependent control of the flavin chemistry will be detected by changes in its redox properties. These investigations will be enriched as well by continuing crystallographic studies of IYD. Finally, the origins of this unusual deiodination will be examined by expressing and characterizing homologous genes from organisms that are successively more distant from mammals in the "Tree of Life." PUBLIC HEALTH RELEVANCE: Iodide is a necessary component of our diet and used to produce an iodide-containing hormone in the thyroid that is required for regulating the metabolic rate of our entire body. The process by which we recycle iodide from byproducts formed during hormone biosynthesis will be investigated and is crucial to understand the basis for certain congenital defects leading to hypothyroidism.
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会议论文
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依托单位:
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TARGET PROMOTED ALKYLATION OF NUCLEIC ACIDS
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Target Promoted Alkylation of Nucleic Acids
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海外基金