Dissecting the Structure and Function of the PDU Microcompartment in Salmonella
解析沙门氏菌 PDU 微区室的结构和功能
基本信息
- 批准号:9055625
- 负责人:
- 金额:$ 48.45万
- 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:2012-05-01 至 2017-04-30
- 项目状态:已结题
- 来源:
- 关键词:Amino AcidsBacteriaBindingBinding ProteinsBiochemicalCaliberCell physiologyComputing MethodologiesCrystallographyDiffusionDrug Delivery SystemsEncapsulatedEnzymesFamilyGenesGeneticGoalsHigher Order Chromatin StructureHomeostasisHomologous GeneHumanIn VitroInvestigationKnowledgeLeadLinkMediatingMetabolicMetabolic PathwayMethodsMicrobeModelingMolecularMovementMutagenesisN-terminalNADHOrganellesPathogenesisPharmacologic SubstancePlayProcessProductionPropylene GlycolsProtein-Protein Interaction MapProteinsPublishingRecyclingResearchRoleSalmonellaSalmonella entericaSalmonella typhimurium LT2Site-Directed MutagenesisSpecificityStructureSubcellular structureSystemTestingWorkbasebiophysical techniquescofactorcytotoxicitydesignenzyme substrateimprovedin vivoinsightmutantpathogenpreventstructural biologysynthetic proteinthree dimensional structuretool
项目摘要
Project Summary: Bacterial microcompartments are large subcellular structures composed of
metabolic enzymes encapsulated within a protein shell built from multiple subunits. They are
widespread among bacteria, functionally diverse, linked to pathogenesis, have a number of
important potential biomedical applications, and appear to incorporate unique mechanistic and
structural principles. Their function is to sequester and regulate the production of toxic or volatile
intermediates found in certain metabolic pathways. However, little is known about how this is
occurs at the mechanistic level. The long-term goal of the proposed research is to elucidate the
molecular principles and to build up a 3-dimensional structure of the microcompartments
involved in 1,2-propanediol degradation by Salmonella. The Salmonella system is unmatched
with regard to the knowledge and tools available for mechanistic studies of microcompartments.
The proposed studies combine genetic, biophysical, and structural methods to elucidate the
cellular function of the Salmonella Pdu microcompartment at a mechanistic level. Three specific
aims are proposed: 1. Determine the role of terminal helixes and other mechanisms for targeting
proteins to the lumen of the Pdu microcompartment; 2. Determine the role of pores and cofactor
recycling in supplying the lumen enzymes of the Pdu microcompartment with required
substrates and cofactors; and 3. Elucidate the higher order structure and assembly of the Pdu
microcompartment. Structures will be investigated and analyzed by x-ray crystallography,
biophysical, and computational methods. Protein-protein binding studies will include his-tag
pulldowns, biophysical methods, and crystallography. Functional and mechanistic insights will
be derived from structure-guided mutagenesis in conjunction with genetic and biochemical
studies. Completion of the proposed investigations will elucidate the mechanistic and structural
principles of the Salmonella pdu microcompartment. This will provide general insights into
bacterial microcompartments. Since bacterial microcompartments play critical metabolic roles in
many microbes, including several human pathogens, the proposed studies may ultimately lead
to new opportunities for interfering with pathogenic processes.
项目概述:细菌微区室是由以下组成的大型亚细胞结构:
由多个亚基组成的蛋白质壳内包裹的代谢酶。他们是
广泛存在于细菌中,功能多样,与发病机制有关,具有许多
重要的潜在生物医学应用,并似乎结合了独特的机制和
结构原则。它们的功能是隔离和调节有毒或挥发性物质的产生,
在某些代谢途径中发现的中间体。然而,很少有人知道这是如何发生的。
发生在机械层面。拟议研究的长期目标是阐明
分子原理并建立微区室的三维结构
参与沙门氏菌降解1,2-丙二醇。沙门氏菌系统是无与伦比的
关于微区室机理研究的知识和工具。
拟议的研究结合联合收割机遗传,生物物理和结构的方法来阐明
沙门氏菌Pdu微区室在机制水平上的细胞功能。三个具体
提出了以下目标:1.确定末端螺旋和其他靶向机制的作用
蛋白质到Pdu微区室的内腔; 2.确定孔隙和辅因子的作用
再循环为Pdu微区室的管腔酶提供所需的
底物和辅因子;和3.阐明Pdu的高阶结构和组装
微区室将通过X射线晶体学研究和分析结构,
生物物理和计算方法。蛋白质-蛋白质结合研究将包括His-标签
下拉、生物物理学方法和晶体学。功能和机械的见解将
来自结构导向诱变结合遗传和生物化学
问题研究完成拟议的调查将阐明机械和结构
沙门氏菌pdu微区室的原理。这将提供一般的见解,
细菌微区室由于细菌微区室在代谢中起着关键的作用,
许多微生物,包括几种人类病原体,拟议的研究可能最终导致
为干扰致病过程提供了新的机会。
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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{{ truncateString('THOMAS Aquinas BOBIK', 18)}}的其他基金
Dissecting the Structure and Function of the PDU Microcompartment in Salmonella
解析沙门氏菌 PDU 微区室的结构和功能
- 批准号:
8459968 - 财政年份:2012
- 资助金额:
$ 48.45万 - 项目类别:
Dissecting the Structure and Function of the PDU Microcompartment in Salmonella
解析沙门氏菌 PDU 微区室的结构和功能
- 批准号:
8373418 - 财政年份:2012
- 资助金额:
$ 48.45万 - 项目类别:
Dissecting the Structure and Function of the PDU Microcompartment in Salmonella
解析沙门氏菌 PDU 微区室的结构和功能
- 批准号:
8646847 - 财政年份:2012
- 资助金额:
$ 48.45万 - 项目类别:
Dissecting the Structure and Function of the PDU Microcompartment in Salmonella
解析沙门氏菌 PDU 微区室的结构和功能
- 批准号:
8839176 - 财政年份:2012
- 资助金额:
$ 48.45万 - 项目类别:
Dissecting the structure, function, and mechanisms of diverse protein-based metabolic organelles in bacteria
剖析细菌中多种基于蛋白质的代谢细胞器的结构、功能和机制
- 批准号:
9333788 - 财政年份:2009
- 资助金额:
$ 48.45万 - 项目类别:
Dissecting the structure and function of the Pdu microcompartment in Salmonella
解析沙门氏菌 Pdu 微区室的结构和功能
- 批准号:
7736996 - 财政年份:2009
- 资助金额:
$ 48.45万 - 项目类别:
Dissecting the structure and function of the Pdu microcompartment in Salmonella
解析沙门氏菌 Pdu 微区室的结构和功能
- 批准号:
7895697 - 财政年份:2009
- 资助金额:
$ 48.45万 - 项目类别:
Dissecting the structure, function, and mechanisms of diverse protein-based metabolic organelles in bacteria
剖析细菌中多种基于蛋白质的代谢细胞器的结构、功能和机制
- 批准号:
9916683 - 财政年份:2009
- 资助金额:
$ 48.45万 - 项目类别:
Conversion of Inactive Cobalamins to Coenzyme B12
无活性钴胺素转化为辅酶 B12
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- 资助金额:
$ 48.45万 - 项目类别:
Conversion of Inactive Cobalamins to Coenzyme B12
无活性钴胺素转化为辅酶 B12
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6671760 - 财政年份:2003
- 资助金额:
$ 48.45万 - 项目类别:
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