Type III Secretion Translocon Structure and Function
Type III Secretion Translocon Structure and Function
批准号:
8701601
负责人:
Arne Rietsch
金额:
$23.78万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-01 至 2016-08-31
关键词:
Aeromonas hydrophilaAntibiotic ResistanceBacteremiaBacteriaBiological AssayBurn injuryBypassCell membraneCellsCorneal InjuryCysteineCytoplasmDataDevelopmentDiseaseDockingDrug TargetingEngineeringErythrocyte MembraneGeneticGenetic TechniquesHeartHospitalsImmune systemIn VitroInfectionInjection of therapeutic agentMapsMembraneMolecularMutationNatureNeedlesNosocomial InfectionsPasteurella pseudotuberculosisPatientsPneumoniaProcessProtein-Protein Interaction MapProteinsPseudomonas aeruginosaResistanceSeverity of illnessStructureSurfaceSyringesTechniquesTestingTherapeutic InterventionType III Secretion System PathwayVentilatorVirulence FactorsWorkantimicrobialcrosslinkdesigndisulfide bonddrug developmentefflux pumphybrid proteinin vivointerestloss of functionmortalitymutantneutrophilpathogenpreventpublic health relevanceresearch studyresistance mechanismsuccess
中文摘要
描述(由申请人提供):铜绿假单胞菌是医院获得性感染的常见原因。它利用III型分泌系统将效应蛋白直接注入目标宿主细胞,特别是中性粒细胞,从而阻止宿主免疫系统的清除。效应蛋白的注射涉及到一种叫做转座子的特殊结构,它由宿主细胞膜上的一个孔组成,与III型分泌针的尖端相互作用。虽然转座子对III型分泌功能至关重要,但对其进行生物化学研究一直很困难。在这里,我们建议使用一种遗传技术来识别关键的易位子相互作用,并根据它们在易位过程中的功能(易位子插入、孔形成、尖端与孔对接以及触发效应分泌)对它们进行分类。识别对功能至关重要的易位接触不仅增加了我们对易位的理解,还确定了潜在的治疗靶点
英文摘要
DESCRIPTION (provided by applicant): P. aeruginosa is a common cause of hospital-acquired infections. It uses a type III secretion system to directly inject effector proteins into targeted host cells, in particular neutrophils, thereby preventing clearance by the host immune system. Injection of effector proteins involves a specialized structure called the translocon, which consists of a pore in the host cell membrane that interacts with the tip of the type III secretion needle. While the translocon is critical for type III secretion function, it has been difficult to study biochemically. Here we propose to use a genetic technique to identify critical translocator interactions and categorize them according to their function in the translocation process (translocator insertion, pore formation, docking of the tip to the pore and triggering of effector secretion). Identifying translocator contacts that are critical for function not only increases our understanding of the translocon, it also identifies potential targets for therapeutic
intervention that lie outside of the bacterial cell and are therefore not shielded by conventional antibiotic resistance mechanisms, such as the outer membrane or efflux pumps.
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会议论文
Host cell factors controlling type III secretion effector translocation
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批准号:10416972
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项目类别:
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资助金额:$24.15万
-
财政年份:2022
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负责人:Arne Rietsch
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依托单位:
Host cell factors controlling type III secretion effector translocation
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批准号:10586145
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项目类别:
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资助金额:$20.13万
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财政年份:2022
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负责人:Arne Rietsch
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依托单位:
Development of recombinase-based tools to study established infections
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批准号:10201472
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项目类别:
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资助金额:$20.13万
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财政年份:2020
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负责人:Arne Rietsch
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依托单位:
Development of recombinase-based tools to study established infections
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批准号:10040615
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项目类别:
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资助金额:$24.14万
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财政年份:2020
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负责人:Arne Rietsch
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依托单位:
P. aeruginosa type III secreted effectors in corneal disease
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批准号:8404007
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项目类别:
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资助金额:$37.29万
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财政年份:2012
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负责人:Arne Rietsch
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依托单位:
P. aeruginosa type III secreted effectors in corneal disease
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批准号:8962457
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项目类别:
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资助金额:$39.63万
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财政年份:2012
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负责人:Arne Rietsch
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依托单位:
P. aeruginosa type III secreted effectors in corneal disease
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批准号:8217524
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项目类别:
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资助金额:$39.25万
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财政年份:2012
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负责人:Arne Rietsch
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依托单位:
P. aeruginosa type III secreted effectors in corneal disease
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批准号:8597435
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项目类别:
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资助金额:$38.47万
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财政年份:2012
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负责人:Arne Rietsch
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依托单位:
P. aeruginosa type III secreted effectors in corneal disease
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批准号:9115162
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项目类别:
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资助金额:$39.63万
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财政年份:2012
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负责人:Arne Rietsch
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依托单位:
海外基金