A systems level analysis of spore coat assembly in Bacillus subtilis
A systems level analysis of spore coat assembly in Bacillus subtilis
批准号:
8307821
负责人:
PATRICK EICHENBERGER
金额:
$29.9万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-01 至 2014-07-31
关键词:
AffectAnimal ModelAnthrax diseaseBacillus (bacterium)Bacillus anthracisBacillus anthracis sporeBacillus subtilisBacteriaBacterial SporesBiochemicalBioterrorismBotulismBreathingCapsid ProteinsCellsChemicalsChimeric ProteinsChromosome MappingClostridiumClostridium botulinumComplexDataDepositionDetectionEncapsulatedEventGenesGeneticGenetic EpistasisGenomicsGerminationGoalsGrowthInfectious AgentInvestigationKineticsLearningLibrariesLifeMapsMediatingMembraneMicrobiologyMolecularNaturePatternPlayProcessProductionPropertyProteinsPublic HealthRegulationRegulonReproduction sporesResearchResistanceRoleSeriesSorting - Cell MovementStructureSurfaceSystemSystems BiologyTechniquesTechnologyTherapeuticToxinTwo-Hybrid System TechniquesYeastscomputerized toolsdesignfunctional genomicsgene discoveryinfancyinsightmutantnovelpathogenpromoterprotein expressionreceptorresearch studyresistance mechanismspatiotemporaltherapeutic developmenttranscription factorweaponsyeast two hybrid system
中文摘要
项目总结
英文摘要
Project summary
Several pathogenic spore-forming bacteria, including the causative agent of anthrax Bacillus anthracis,
are inhaled or ingested as spores and resume growth and toxin production in the host after germination. The
spore protein coat, which encapsulates the spore, is an important factor in the infectious cycle, because of its
effective protective function and its regulatory role in the germination process by controlling access of
germinants to receptors located in the inner membrane of the spore. The spore coat is a morphologically
complex structure composed of approximately 60 different sporulation proteins that assemble around the
nascent spore. In this proposal, we will use an integrated systems biology approach to map protein interaction
networks and identify key regulatory hubs that nucleate spore coat assembly- which may serve as markers for
spore detection and/or as targets for control of spore germination in applications against bioterrorism. In
addition to its relevance to public health issues, we envision that our project will illustrate the value of systems
biology approaches for investigating the assembly of complex structures.
We propose to use high throughput protein localization screens to characterize the protein interaction
networks that govern spore coat assembly in the model organism Bacillus subtilis. Specifically, we will use a
library of fluorescent protein fusions to all of the coat proteins in B. subtilis, to define the spatiotemporal
hierarchy of deposition of spore coat proteins around the spore, to identify which morphogenetic proteins are
required for the recruitment of all spore coat proteins and learn the transcriptional and post-translational
mechanisms underlying the regulation of coat assembly. The nature of the interactions established between
pairs of coat proteins will be demonstrated using a large scale yeast two hybrid assay and various focused
biochemical approaches. Finally, we will use computational tools to integrate the data gathered from these
experiments and obtain a comprehensive representation of the spore coat protein interaction network that will
serve as a template for the study of other spore-forming bacteria, particularly B. anthracis.
1 Project narrative
Our research will derive new hypotheses and mechanisms for the resistance
properties of Bacillus spores and the mechanisms that control spore germination. We
anticipate that our results will have an impact on the design of therapeutic approaches to
detect and eliminate pathogenic spore-forming bacteria.
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DOI:
10.1111/j.1365-2958.2012.08003.x
发表时间:
2012-03
期刊:
Molecular microbiology
影响因子:
3.6
作者:
[Cozy LM, Phillips AM, Calvo RA, Bate AR, Hsueh YH, Bonneau R, Eichenberger P, Kearns DB]
通讯作者:
Kearns DB
DOI:
10.1111/mmi.14116
发表时间:
2018-11
期刊:
Molecular microbiology
影响因子:
3.6
作者:
[Nunes F, Fernandes C, Freitas C, Marini E, Serrano M, Moran CP Jr, Eichenberger P, Henriques AO]
通讯作者:
Henriques AO
DOI:
10.1371/journal.pgen.1004636
发表时间:
2014-10
期刊:
PLoS genetics
影响因子:
4.5
作者:
[Abe K, Kawano Y, Iwamoto K, Arai K, Maruyama Y, Eichenberger P, Sato T]
通讯作者:
Sato T
DOI:
10.1016/j.cub.2010.06.031
发表时间:
2010-09-14
期刊:
CURRENT BIOLOGY
影响因子:
9.2
作者:
[de Hoon, Michiel J. L., Eichenberger, Patrick, Vitkup, Dennis]
通讯作者:
Vitkup, Dennis
DOI:
10.1371/journal.pcbi.1002228
发表时间:
2011-12
期刊:
PLoS computational biology
影响因子:
4.3
作者:
[Kacmarczyk T, Waltman P, Bate A, Eichenberger P, Bonneau R]
通讯作者:
Bonneau R
共 9 条
A systems level analysis of spore coat assembly in Bacillus subtilis
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批准号:7678534
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项目类别:
-
资助金额:$29.67万
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财政年份:2008
-
负责人:PATRICK EICHENBERGER
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依托单位:
A systems level analysis of spore coat assembly in Bacillus subtilis
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批准号:8120825
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项目类别:
-
资助金额:$29.1万
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财政年份:2008
-
负责人:PATRICK EICHENBERGER
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依托单位:
A systems level analysis of spore coat assembly in Bacillus subtilis
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批准号:7905204
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项目类别:
-
资助金额:$29.2万
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财政年份:2008
-
负责人:PATRICK EICHENBERGER
-
依托单位:
A systems level analysis of spore coat assembly in Bacillus subtilis
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批准号:7466144
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项目类别:
-
资助金额:$29.98万
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财政年份:2008
-
负责人:PATRICK EICHENBERGER
-
依托单位:
海外基金