Synthetic Chemical Biology
合成化学生物学
基本信息
- 批准号:10245047
- 负责人:
- 金额:$ 16.16万
- 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
- 起止时间:2012-07-15 至 2023-06-30
- 项目状态:已结题
- 来源:
- 关键词:AddressAnimal ModelAnti-Infective AgentsBiochemistryBiologicalBiological AssayBiologyBiomedical ResearchBiotinCell Culture TechniquesCell modelCellsCellular AssayCenters of Research ExcellenceChemicalsChemistryClientCommunicable DiseasesCommunitiesCore FacilityCustomDNA Sequencing FacilityDisease PathwayEquipmentEvaluationFacultyFoundationsFundingGenerationsGenesGoalsGrantHuman ResourcesImaging DeviceIn VitroInfrastructureKansasLabelLeadMethodsMicrofabricationMicrofluidicsMicroscopyMissionModelingMolecularMolecular AnalysisMolecular ProbesNational Institute of General Medical SciencesOrganic ChemistryPeptidesPharmaceutical ChemistryPhasePropertyResearch PersonnelResolutionResourcesRodentServicesStructureTracerUniversitiesWorkZebrafishbiological systemscellular imagingchemical synthesisdesigndrug discoveryexperiencefluorescence imagingfluorophoregenome sequencinghigh resolution imaginghigh throughput screeningimprovedin vivonoveloperationoutreachpeptidomimeticsprogramssmall moleculesuccess
项目摘要
PROJECT SUMMARY
The Synthetic Chemical Biology Core (SCBC) was established in July 2016 from the merger of the Center for
Molecular Analysis of Disease Pathways (CMADP) Molecular Probes Core (MPC) with the newly established
Chemical Biology of Infectious Disease (CBID) Medicinal Chemistry Core (MCC). The synthetic capabilities of
the SCBC will fulfill the specific aims of both COBRE centers. The mission for the SCBC in Phase II is to provide
the junior faculty affiliated with CMADP, as well as other investigators in the state of Kansas, with novel molecular
probes of biological systems. The SCBC will also offer the capability to evaluate these probes in vitro in whole-
cell bioassays, and in vivo in zebrafish, an increasingly important model organism for biomedical research. The
SCBC will also fulfill CBID’s missions concerning anti-infective drug discovery. These projects will be funded
through the CBID. The SCBC Director is responsible for coordinating all SCBC Core lab activities to both COBRE
centers. The SCBC will offer expert design of molecular probes and synthesis of both small molecules and
peptides, with an emphasis on the generation of fluorescent and other tagged molecules. SCBC will also offer
bioassays of molecular probes, including whole cell assays and assays using zebrafish, to bridge a gap that
currently exists between very high resolution imaging of cells in culture and low resolution imaging of fluorescent
tracers in rodents. The newly established SCBC would function synergistically with other CMADP-funded Core
facilities, including the Genome Sequencing Core, to identify genes that impact functions of probes in vivo, and
the Microfabrication and Microfluidics Core, to develop devices for imaging and chemical analysis. This
integration is designed to empower faculty to use chemical biology approaches to investigate biological
problems.
The SCBC provides investigators with access to highly qualified personnel with experience in synthetic organic
chemistry, biochemistry, microscopy, and approaches for optimization of biological properties of synthetic
molecules. The Center has two Co-Core Leaders from the Department of Medicinal Chemistry at KU. Prof. Blake
Peterson will continue to be the Leader of the CMADP’s part of the SCBC. Prof. Tom Prisinzano is the Leader
of the CBID part of the SCBC. The Director of SCBC is Dr. Chamani Perera. The specific aims that will be
addressed by the SCBC for this Phase II proposal are: (1) to continue to integrate resources from the proposed
COBRE Center for Molecular Analysis of Disease Pathways Phase II with the existing COBRE Center for
Chemical Biology of Infectious Disease Phase I to further establish the new SCBC, gain economies of scale,
and serve faculty affiliated with the COBRE CMADP; (2) design and synthesize molecular probes of biological
systems for faculty investigators; (3) enable faculty clients to conduct bioassays in cell culture and zebrafish
models; and (4) provide outreach and administrative support necessary to manage Core activities, and offer
services to the larger biomedical research community in the state of Kansas.
项目总结
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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BLAKE PETERSON其他文献
BLAKE PETERSON的其他文献
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{{ truncateString('BLAKE PETERSON', 18)}}的其他基金
Synthetic Lethal Targeting of Growth Factor Receptors
生长因子受体的合成致死靶向
- 批准号:
9218305 - 财政年份:2017
- 资助金额:
$ 16.16万 - 项目类别:
Synthetic Lethal Targeting of Growth Factor Receptors
生长因子受体的合成致死靶向
- 批准号:
10065292 - 财政年份:2017
- 资助金额:
$ 16.16万 - 项目类别:
Tissue-specific delivery of probes by control of membrane trafficking of endoprot
通过控制内切酶的膜运输实现探针的组织特异性递送
- 批准号:
7817256 - 财政年份:2009
- 资助金额:
$ 16.16万 - 项目类别:
Tissue-specific delivery of probes by control of membrane trafficking of endoprot
通过控制内切酶的膜运输实现探针的组织特异性递送
- 批准号:
7937894 - 财政年份:2009
- 资助金额:
$ 16.16万 - 项目类别:
University of Kansas/Haskell Indian Nations University IRACDA Project
堪萨斯大学/哈斯克尔印第安民族大学 IRACDA 项目
- 批准号:
8708099 - 财政年份:2002
- 资助金额:
$ 16.16万 - 项目类别:
University of Kansas/Haskell Indian Nations University IRACDA Project
堪萨斯大学/哈斯克尔印第安民族大学 IRACDA 项目
- 批准号:
9527924 - 财政年份:2002
- 资助金额:
$ 16.16万 - 项目类别:
University of Kansas/Haskell Indian Nations University IRACDA Project
堪萨斯大学/哈斯克尔印第安民族大学 IRACDA 项目
- 批准号:
8367984 - 财政年份:2002
- 资助金额:
$ 16.16万 - 项目类别:
University of Kansas/Haskell Indian Nations University IRACDA Project
堪萨斯大学/哈斯克尔印第安民族大学 IRACDA 项目
- 批准号:
8516517 - 财政年份:2002
- 资助金额:
$ 16.16万 - 项目类别:
University of Kansas/Haskell Indian Nations University IRACDA Project
堪萨斯大学/哈斯克尔印第安民族大学 IRACDA 项目
- 批准号:
8898829 - 财政年份:2002
- 资助金额:
$ 16.16万 - 项目类别:
RECEPTOR MEMBRANE ANCHORING WITH SYNTHETIC ANTIESTROGENS
用合成抗雌激素锚定受体膜
- 批准号:
6489325 - 财政年份:2000
- 资助金额:
$ 16.16万 - 项目类别:
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