A fluorescence displacement assay for BioA: An enzyme involved in biotin biosynth
A fluorescence displacement assay for BioA: An enzyme involved in biotin biosynth
批准号:
8262096
负责人:
Courtney C Aldrich
金额:
$3.78万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-01-01 至 2013-12-31
关键词:
AIDS-Related Opportunistic InfectionsAcyl Coenzyme AAnabolismAntitubercular AgentsAntsAtypical MycobacteriaBacillus (bacterium)BiochemicalBiologicalBiological AssayBiotinBiotin Metabolism PathwayCarbon DioxideCell DeathCellsCessation of lifeChemicalsChronicCommunicable DiseasesCoupledCouplingCustomDataDetectionDevelopmentDrug Delivery SystemsDrug resistanceEnzymesExtreme drug resistant tuberculosisFluorescenceFluorescent ProbesGeneticGluconeogenesisHousingIn VitroInfectionLabelLaboratoriesLeadLibrariesMeasuresMetabolicMicrobiologyModelingMolecular BankMulti-Drug ResistanceMultidrug-Resistant TuberculosisMusMycobacterium smegmatisMycobacterium tuberculosisMycobacterium tuberculosis H37RvNatureNutrientPathway interactionsPatientsPersonsPhasePhenotypePlagueProductionPyruvate CarboxylaseReactionReagentRecombinant ProteinsRelative (related person)ResearchScreening procedureSeriesSourceSpecificityStaining methodStainsStarvationStreptavidinSystemTuberculosisValidationVirulenceVirulentVitaminsbasecofactordesigndesthiobiotindrug developmentdrug discoveryenzyme substratefatty acid metabolismgenome sequencinghigh throughput screeningin vivomedical schoolsmortalitymutantnoveloverexpressionpathogenresistant strainresponsesmall moleculetuberculosis drugs
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Mycobacterium tuberculosis is the leading cause of bacterial infectious disease deaths worldwide. Drug-resistant strains (MDR and XDR-TB) are an emerging problem and could lead to significant issues in the US because over half of the cases are in foreign born persons. Biotin biosynthesis has recently been identified as an attractive target for the development of new ant tubercular agents. In this proposal we describe the design, development, and optimization of a novel HTS-assay for BioA, which catalyzes the second step of biotin biosynthesis in Mtb. The objectives of this application are to screen BioA using our novel HTS assay and then perform secondary and tertiary screening of identified hits. In the first specific aim, we will prepare chemical and biochemical reagents for the primary and secondary assays. In the second specific aim, we will develop and screen hits using an orthogonal LC-MS based assay. In the third specific aim, we will perform tertiary screening using mutant strains of M. smegmatis that over- and under-express BioA to access biological activity and characterize on-target specificity.
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海外基金