NOVEL DRUG DESIGN AND HIGH THROUGHPUT SCREENING
NOVEL DRUG DESIGN AND HIGH THROUGHPUT SCREENING
批准号:
7902212
负责人:
EDITH PORTER
金额:
$34.45万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
Acquired Immunodeficiency SyndromeAddressAnti-Bacterial AgentsAntibiotic ResistanceAntibioticsArginineBe++ elementBerylliumBindingBiologicalBiological AssayBiological FactorsBiological ModelsBody FluidsCatalysisCategoriesCationsChemical StructureChemicalsClinicalCollaborationsCollectionCommunicable DiseasesComplement component C1sCore FacilityDataDevelopmentDiagnosisDiagnosticDiseaseDrug Delivery SystemsDrug DesignDrug resistanceEmergency SituationEnzymesEssential GenesEventExploratory/Developmental GrantFacultyFoundationsFrequenciesFundingFunding MechanismsGenetic PolymorphismGenomeGenomicsGoalsGrowthHIVHealthcareHost DefenseHuman bodyIndiumIndividualInfectious AgentInstitutionKnowledgeLaboratoriesLeadLibrariesLigandsLinkLipidsMalariaMeasuresMentorsMethodsMicrobial GeneticsMinorityModelingMolecularMolecular AnalysisMulti-Drug ResistanceMycobacterium tuberculosisNatural ImmunityNaturePatientsPeptidesPharmaceutical PreparationsPharmacogeneticsPharmacologic SubstancePlasmodium falciparumPlayPopulationProteinsReportingResearchResearch InfrastructureResearch PersonnelResistanceRespiratory SystemRespiratory tract structureRoleScaffolding ProteinSchemeScreening procedureSevere Acute Respiratory SyndromeSocioeconomic FactorsStaphylococcus aureusStreptococcus pneumoniaeSystemTechniquesTestingTherapeuticTryptophanTuberculosisVariantWorkalpha helixantimicrobialantimicrobial drugbasebiological systemscareer developmentcellular targetingcombatdesigndisease phenotypedrug candidatedrug discoverydrug resistant bacteriafight againstflexibilityfunctional genomicshealth disparityhigh throughput screeningin vivoinhibitor/antagonistinnovationinsightinstrumentationinterestknowledge basemicrobialmolecular recognitionnovelnovel strategiesoptimismpathogenprogramsprotein structureresistant strainresponsesmall moleculesocialsocial disparitiestool development
中文摘要
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英文摘要
Development of novel antibiotics is of utmost urgency, considering the increase in multi-drug resistant strains
in diseases like tuberculosis, malaria, AIDS, and the emergence of hitherto unknown diseases such as
SARS. Infectious diseases, especially those that involve drug resistant pathogens, have been exacerbated
by socioeconomic factors, resulting in widespread health disparities among minority populations. Our long
term objective is to discover and develop novel antibiotics to combat infectious diseases (in particular those
caused by drug resistant pathogens), contributing to the effort of elimination of health disparities. As a
subproject of an application for Research Infrastructure in Minority Institutions (RIMI) Program support, we
propose to advance antibiotic drug discovery through complementary and integrated novel approaches from
the host defense, the microbial genomic, and the fundamental molecular recognition perspectives. In
particular, we will assess the potential of natural host defense lipids as antimicrobial therapeutics, building on
the foundation of our recent experimental data in support of lipids' novel in vivo defensive roles. On another
front, we will leverage the increased research capacity to identify additional novel chemical structures with
antimicrobial activities through high throughput screening of diverse compound libraries. Anticipating a
steady provision of potent antibacterial compounds, we will attempt to develop a novel and more efficient
method of identifying the cellular targets for these potent inhibitors (including lipid-based inhibitors) through
modulated expression of essential target proteins. Furthermore, we will probe and evaluate the molecular
cation-pi interaction as a potential novel mechanism of ligand-protein recognition and binding, the result of
which would provide new insight and strategies for rational drug design for those newly discovered and
prioritized antimicrobial target-inhibitor pairs. With guidance from internal and external mentors and access
to high throughput screening and chemical/molecular analysis instrumentation through RIMI funding
mechanism, the investigators will be able establish a novel and integrated drug discovery platform that will
contribute to the fight against drug resistant pathogens and the effort to eliminate health disparities among
minority populations.
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会议论文
Lipid Effector Molecules of Innate Immunity: Antimicrobial Cholesteryl Esters
-
批准号:8475619
-
项目类别:
-
资助金额:$27.99万
-
财政年份:2011
-
负责人:EDITH PORTER
-
依托单位:
Lipid Effector Molecules of Innate Immunity: Antimicrobial Cholesteryl Esters
-
批准号:8274652
-
项目类别:
-
资助金额:$30.15万
-
财政年份:2011
-
负责人:EDITH PORTER
-
依托单位:
Lipid Effector Molecules of Innate Immunity: Antimicrobial Cholesteryl Esters
-
批准号:8668077
-
项目类别:
-
资助金额:$29.0万
-
财政年份:2011
-
负责人:EDITH PORTER
-
依托单位:
Lipid Effector Molecules of Innate Immunity: Antimicrobial Cholesteryl Esters
-
批准号:8078425
-
项目类别:
-
资助金额:$29.75万
-
财政年份:2011
-
负责人:EDITH PORTER
-
依托单位:
NOVEL DRUG DESIGN AND HIGH THROUGHPUT SCREENING
-
批准号:7161228
-
项目类别:
-
资助金额:$16.12万
-
财政年份:2005
-
负责人:EDITH PORTER
-
依托单位:
Lipids: Effectors in Innate Immunity
-
批准号:6825790
-
项目类别:
-
资助金额:$19.33万
-
财政年份:2004
-
负责人:EDITH PORTER
-
依托单位:
Lipids: Effectors in Innate Immunity
-
批准号:6913701
-
项目类别:
-
资助金额:$17.65万
-
财政年份:2004
-
负责人:EDITH PORTER
-
依托单位:
NOVEL DRUG DESIGN AND HIGH THROUGHPUT SCREENING
-
批准号:7547671
-
项目类别:
-
资助金额:$14.08万
-
财政年份:--
-
负责人:EDITH PORTER
-
依托单位:
NOVEL DRUG DESIGN AND HIGH THROUGHPUT SCREENING
-
批准号:7682570
-
项目类别:
-
资助金额:$34.7万
-
财政年份:--
-
负责人:EDITH PORTER
-
依托单位:
NOVEL DRUG DESIGN AND HIGH THROUGHPUT SCREENING
-
批准号:7547674
-
项目类别:
-
资助金额:$33.84万
-
财政年份:--
-
负责人:EDITH PORTER
-
依托单位:
海外基金