Center for Biomolecular Structure and Dynamics
生物分子结构与动力学中心
基本信息
- 批准号:8730685
- 负责人:
- 金额:$ 198.2万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2011
- 资助国家:美国
- 起止时间:2011-09-01 至 2016-07-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAdenylate CyclaseAmino AcidsArenavirusBinding SitesBiochemicalBiochemistryBiologicalBiological SciencesBiologyBiophysicsCatabolismCatalysisCellsCenters of Research ExcellenceChemicalsChemistryCollaborationsCore FacilityDioxygenasesEnzymesEsapentFacultyFloorFoundationsFundingGlycoproteinsGoalsHomology ModelingHumanInfectionInterdisciplinary StudyInvestigationJunin virusLigand BindingLigandsMagnetismMediatingMembrane FusionMembrane ProteinsMental disordersMentorsMentorshipMetabolismMethodsMolecularMolecular ComputationsMolecular MachinesMolecular StructureMontanaMulti-Drug ResistanceNuclearOpioid ReceptorPerceptionPharmacologic SubstancePhysiologyPlant RootsPositioning AttributePropertyRecruitment ActivityResearchResearch InfrastructureResearch PersonnelResearch Project GrantsResearch SupportScienceSelf AssessmentSignal TransductionSpectrum AnalysisStructureSystemTertiary Protein StructureTheoretical BiologyTryptophanUniversitiesViralViral ProteinsVisionX ray diffraction analysisX-Ray CrystallographyX-Ray Diffractionbasechemical geneticscomputational chemistrydesignempoweredenzyme mechanismhuman diseaseindoleamineinfrastructure developmentinnovationinterestmembermolecular dynamicsmultidisciplinaryprogramsprotein complexquantum chemistryresearch facilityresearch studystructural biology
项目摘要
The Center for Biomolecular Structure and Dynamics (CBSD) at the University of Montana (UM) is rooted in structural biology but multidisciplinary in scope. The rationale that underlies this program is based on the perception that effective biomedical innovation is driven from an understanding of macromolecular structure, which in turn, must be grounded on principles of experimental and theoretical chemistry. CBSD faculty are drawn from Department of Chemistry & Biochemistry, the Division of Biological Science and the Department of Biomedical and Pharmaceutical Sciences. Among this group are CBSD faculty with expertise in spectroscopy, structural biology, biochemistry and mechanistic and theoretical chemistry. We build on a strong foundation of sustained institutional support. Associated with the CBSD is a newly established interdisciplinary graduate program in Biochemistry and Biophysics. The goal of the proposed COBRE is to integrate investigators with research interests in cell and molecular physiology, mechanistic biochemistry, chemical biology, and theoretical and computational chemistry, into an interactive and collaborative network. With the creation of a CBSD COBRE, it is our goal to give structure to this vision by implementing the four aims of this proposal:
Aim 1. Provide research support for five interdisciplinary research projects within the COBRE theme. These projects use theoretical and physical chemical methods to elucidate the catalytic mechanisms of enzymes involved in signal transduction and tryptophan catabolism. Structure-based homology modeling and chemical biology approaches will be used to design new ligands for the opioid receptor and to characterize the binding sites of the multidrug resistance transporter. Heteronuclear NMR experiments will be used to elucidate the structures of critical domains in the Junin arenavirus membrane fusion glycoprotein. Aim 2 shall be to recruit two new faculty members to CBSD-affiliated departments to build on existing strengths and introduce new expertise within the CBSD. Aim 3 will support collaborative activities involving CBSD faculty by sustaining of critical core research facilities in Macromolecular X-ray diffraction, Macromolecular NMR, BioSpectroscopy and Molecular Computation. Aim 4 will establish a supportive program to sustain an intellectually vibrant and cohesive CBSD that promotes infrastructure development, mentoring, scientific exchange and collaboration, with a robust advisory and self-assessment structure.
蒙大拿州大学(UM)的生物分子结构与动力学中心(CBSD)植根于结构生物学,但范围涉及多学科。该计划的基本原理是基于这样一种认识,即有效的生物医学创新是由对大分子结构的理解驱动的,而大分子结构又必须以实验和理论化学原理为基础。教职员工来自化学与生物化学系、生物科学系和生物医学与制药科学系。在这个群体中,CBSD的教师在光谱学,结构生物学,生物化学以及机械和理论化学方面具有专业知识。我们建立在持续的机构支持的坚实基础上。与CBSD相关的是一个新建立的生物化学和生物物理学跨学科研究生课程。拟议的COBRE的目标是将研究人员与细胞和分子生理学,机械生物化学,化学生物学,理论和计算化学的研究兴趣整合到一个互动和协作的网络中。随着CBSD COBRE的建立,我们的目标是通过实施本提案的四个目标来构建这一愿景:
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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Stephen R Sprang其他文献
Stephen R Sprang的其他文献
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{{ truncateString('Stephen R Sprang', 18)}}的其他基金
Mechanism of G protein Activation by Ric-8A - competitive revision of R01GM105993
Ric-8A 激活 G 蛋白的机制 - R01GM105993 的竞争性修订版
- 批准号:
8960270 - 财政年份:2013
- 资助金额:
$ 198.2万 - 项目类别:
Macromolecular X-ray Diffraction Core Research Facility
高分子X射线衍射核心研究设施
- 批准号:
10004084 - 财政年份:2011
- 资助金额:
$ 198.2万 - 项目类别:
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