Structural Biology Core
Structural Biology Core
批准号:
10017157
负责人:
Karson Putt
金额:
$101.14万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-30 至 2024-08-31
关键词:
Alzheimer&aposs DiseaseBindingBinding ProteinsBinding SitesBiological AssayBiological ProcessBiophysicsComputer AnalysisComputer AssistedComputer ModelsComputer SimulationComputing MethodologiesCore FacilityCryoelectron MicroscopyCrystallizationCrystallographyDataDrug DesignElectron Microscopy FacilityEvaluationGenerationsGoalsHomology ModelingIn VitroLeadLigand BindingMethodsModelingMolecularMolecular StructurePharmaceutical PreparationsPostdoctoral FellowPropertyProteinsPublishingResolutionSchemeScientistStructureStructure-Activity RelationshipTestingValidationWorkX ray diffraction analysisX-Ray Crystallographybasedesigndoctoral studentdrug discoveryhigh throughput screeningin silicoin vitro Assayin vivoinsightlead optimizationmodels and simulationnovel lead compoundprocess optimizationprotein protein interactionprotein structuresmall moleculestructural biology
中文摘要
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英文摘要
PROJECT SUMMARY Structural Biology & Biophysics Core
The goal of the Structural Biology & Biophysics (SBB) Core is to help achieve the overall ADDD CENTER aim
of developing high quality lead compounds for novel Alzheimer's Disease (AD) targets (Overall MILESTONE 3).
The SBB Core will work in concert with the other Technical Cores to provide computer aided drug design for hit
generation and optimization, co-crystallization for structure guided design, and target structural information for
Target Enablement Packages (TEPs). The SBB Core will enable the identification of hit molecules by first
elucidating unknown structures for prioritized ADDD CENTER targets via x-ray diffraction or cryo-electron
microscopy, then utilizing those structures (or already known published structures) to perform computer aided
drug design via multiple in silico methods. Prioritized molecules will be synthesized by the MCCB Core and
evaluated in target specific in vitro assay flow schemes (ADHTS Core) to complete the iteration cycle. To further
aid in the structure activity relationship analysis and hit-to-lead optimization process, co-crystals of the protein
target and newly designed small molecule binders will be grown and diffracted. The data will be utilized for
structure guided design to optimize interactions between the ligand and protein binding sites. Through the
contributions of the SBB Core, rapid progress will be made by ADDD CENTER scientists in optimizing hits into
lead molecules through both computational simulations and structural studies that help establish connectivity
between molecular design and biological function.
The SBB Core is led by Drs. Andrew Mesecar and Markus Lill who are responsible for the two components of
the core, crystallography/structure determination and computer aided drug design, respectively. The
composition of the SBB Core will primarily consist of graduate and post-doctoral students. Additionally, staff
from Purdue's extensive core facilities, including the Macromolecular crystallography and cryo-electron
microscopy facility, will support SBB Core activities.
The Specific Aims of the SBB Core are:
Specific Aim 1: Identification of structure based design-amenable nominated targets.
Specific Aim 2: Elucidate target structures to guide drug discovery activities.
Specific Aim 3: Predict and design potential hit molecular structures for iterative molecular design,
synthesis, and testing.
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Structural Biology Core
-
批准号:10684141
-
项目类别:
-
资助金额:$82.63万
-
财政年份:2019
-
负责人:Karson Putt
-
依托单位:
Structural Biology Core
-
批准号:10250438
-
项目类别:
-
资助金额:$88.51万
-
财政年份:2019
-
负责人:Karson Putt
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依托单位:
国内基金
海外基金
新型F-18标记香豆素衍生物PET探针的研制及靶向Alzheimer's Disease 斑块显像研究
-
批准号:81000622
-
项目类别:青年科学基金项目
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资助金额:20.0万元
-
批准年份:2010
-
负责人:梁胜
-
依托单位:
阿尔茨海默病(Alzheimer's disease,AD)动物模型构建的分子机理研究
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批准号:31060293
-
项目类别:地区科学基金项目
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资助金额:26.0万元
-
批准年份:2010
-
负责人:郭亚芬
-
依托单位:
跨膜转运蛋白21(TMP21)对引起阿尔茨海默病(Alzheimer'S Disease)的γ分泌酶的作用研究
-
批准号:30960334
-
项目类别:地区科学基金项目
-
资助金额:22.0万元
-
批准年份:2009
-
负责人:董贵成
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依托单位: