Ras Signaling in C. neoformans virulence and development
Ras Signaling in C. neoformans virulence and development
批准号:
8033188
负责人:
ANDREW ALSPAUGH
金额:
$30.58万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-12-15 至 2013-03-31
关键词:
AffectAnti-Infective AgentsBiological ModelsCell SizeCell physiologyCellsCellular StressCryptococcus neoformansCytoskeletonDataDevelopmentEmployee StrikesEnvironmentEventGene TargetingGenetic TranscriptionGoalsGrowthHumanInfectionModificationMolecularMorphogenesisOrganismParasitesPathogenesisPathway interactionsProcessProteinsRoleSeriesShapesSignal PathwaySignal TransductionSignal Transduction PathwaySignaling MoleculeSignaling ProteinSpecificityStressTemperatureVirulencearmcomparativedesignfungushuman diseaseinfectious disease treatmentmicrobialmicroorganismmutantpathogenprotein functionras Proteinsresearch studyresponsesingle molecule
中文摘要
描述(申请人提供):项目总结。导致人类疾病的微生物必须能够对宿主环境中遇到的压力做出反应。这些细胞反应包括形态发生的改变,或细胞骨架的改变,这些改变决定了细胞的大小、形状和体积。这项提议的长期目标是定义允许微生物病原体调节这些过程并适应受感染宿主的敌对环境的分子事件。人类真菌病原体新生隐球菌是理解微生物发病机制基本问题的重要模型系统。作为对宿主-寄生虫相互作用过程中遇到的压力的反应,新生隐孢子虫的细胞骨架显示出可复制的变化。这些形态发生反应使细胞能够适应高温和其他宿主特有的条件。Ras1蛋白控制着指导许多适应性细胞反应的细胞内信号事件。这项提议中的实验将定义新生芽孢杆菌利用Ras1和一系列级联的蛋白质相互作用在宿主内生存和生长的方式。首先,将研究Ras1形态发生途径的独特成分,以确定这些蛋白质如何在37℃下特异性地指导形态发生和生长。其次,将创建一个微阵列数据概要,以更全面地定义那些在Ras1信号通路的不同臂中发挥功能的蛋白质。最后,将研究RAS蛋白在细胞内的定位,以确定其在确定微生物病原体中RAS信号特异性方面的作用。相关性:。确定微生物与宿主相互作用的方式将有助于更好地了解和治疗传染病。这项建议中的研究将描述RAS蛋白允许微生物对受感染宿主内遇到的压力做出反应的方式。RAS及其相关蛋白的操纵直接影响微生物的生存,为新的抗感染疗法的开发提供了独特的选择。
叙述:定义微生物与宿主相互作用的方式将有助于更好地理解和治疗传染病。这项建议中的研究将描述RAS蛋白允许微生物对受感染宿主内遇到的压力做出反应的方式。RAS及其相关蛋白的操纵直接影响微生物的生存,为新的抗感染疗法的开发提供了独特的选择。
英文摘要
DESCRIPTION (provided by applicant): Project summary. Microorganisms that cause human disease must be able to respond to stresses encountered in the host environment. These cellular responses include morphogenic changes, or modifications of the cytoskeleton that determine cell size, shape, and volume. The long-term goals of this proposal are to define the molecular events that allow microbial pathogens to regulate these processes and adapt to the hostile environment of the infected host. The human fungal pathogen Cryptococcus neoformans is an important model system for understanding basic issues in microbial pathogenesis. In response to stresses encountered during a host-parasite interaction, C. neoformans displays reproducible alterations in its cytoskeleton. These morphogenic responses allow the cell to adapt to elevated temperatures and other host-specific conditions. The Ras1 protein controls the intracellular signaling events that direct many of these adaptive cellular responses. The experiments in this proposal will define the ways in which C. neoformans uses Ras1 and a cascading series of protein interactions to survive and grow within the host. First, unique components of the Ras1 morphogenesis pathways will be studied to determine how these proteins specifically direct morphogenesis and growth at 37C. Second, a compendium of microarray data will be created to more fully define those proteins that function in the various arms of the Ras1 signaling pathways. Finally, Ras protein localization within the cell will be studied to define its role in determining Ras signaling specificity in a microbial pathogen. Relevance:. Defining the ways in which microorganisms interact with their host will result in better understanding and treatment of infectious diseases. The studies in this proposal will characterize the ways in which Ras proteins allow microorganisms to respond to the stresses encountered within the infected host. Manipulation of Ras and its related proteins directly affects microbial survival and offers a unique option for the development of new anti-infective therapies.
NARRATIVE : Defining the ways in which microorganisms interact with their host will result in better understanding and treatment of infectious diseases. The studies in this proposal will characterize the ways in which Ras proteins allow microorganisms to respond to the stresses encountered within the infected host. Manipulation of Ras and its related proteins directly affects microbial survival and offers a unique option for the development of new anti-infective therapies.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Coordinated responses to host-derived stresses in C. neoformans
-
批准号:10637411
-
项目类别:
-
资助金额:$36.02万
-
财政年份:2023
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Arrestin proteins mediate microbial cellular adaptation and fungal virulence
-
批准号:10369482
-
项目类别:
-
资助金额:$24.15万
-
财政年份:2022
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Arrestin proteins mediate microbial cellular adaptation and fungal virulence
-
批准号:10612333
-
项目类别:
-
资助金额:$20.13万
-
财政年份:2022
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Coordinated Regulation of Virulence Genes in C. neoformans
-
批准号:8859954
-
项目类别:
-
资助金额:$38.59万
-
财政年份:2011
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Coordinated Regulation of Virulence Genes in C. neoformans
-
批准号:8493973
-
项目类别:
-
资助金额:$36.31万
-
财政年份:2011
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Coordinated Regulation of Virulence Genes in C. neoformans
-
批准号:8292127
-
项目类别:
-
资助金额:$38.65万
-
财政年份:2011
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Coordinated Regulation of Virulence Genes in C. neoformans
-
批准号:8068059
-
项目类别:
-
资助金额:$38.21万
-
财政年份:2011
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Coordinated Regulation of Virulence Genes in C. neoformans
-
批准号:8668884
-
项目类别:
-
资助金额:$38.61万
-
财政年份:2011
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Coordinated Regulation of Virulence Genes in C. neoformans
-
批准号:7809263
-
项目类别:
-
资助金额:$30.34万
-
财政年份:2009
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Coordinated Regulation of Virulence Genes in C. neoformans
-
批准号:8080553
-
项目类别:
-
资助金额:$30.46万
-
财政年份:2009
-
负责人:ANDREW ALSPAUGH
-
依托单位:
C. neoformans cAMP signaling and pathogenesis
-
批准号:7245424
-
项目类别:
-
资助金额:$31.1万
-
财政年份:2006
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Molecular Mycology and Pathogenesis Training Program
-
批准号:10408064
-
项目类别:
-
资助金额:$43.94万
-
财政年份:2003
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Molecular Mycology and Pathogenesis Training Program
-
批准号:10179298
-
项目类别:
-
资助金额:$41.14万
-
财政年份:2003
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Molecular Mycology and Pathogenesis Training Program
-
批准号:10630207
-
项目类别:
-
资助金额:$43.71万
-
财政年份:2003
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Molecular Mycology and Pathogenesis Training Program
-
批准号:9790417
-
项目类别:
-
资助金额:$41.53万
-
财政年份:2003
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Ras signaling in C. neoformans virulence and development
-
批准号:6825749
-
项目类别:
-
资助金额:$30.8万
-
财政年份:2002
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Ras Signaling in C. neoformans virulence and development
-
批准号:7768467
-
项目类别:
-
资助金额:$30.89万
-
财政年份:2002
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Ras Signaling in C. neoformans virulence and development
-
批准号:8237050
-
项目类别:
-
资助金额:$30.58万
-
财政年份:2002
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Ras signaling in C. neoformans virulence and development
-
批准号:6571725
-
项目类别:
-
资助金额:$15.08万
-
财政年份:2002
-
负责人:ANDREW ALSPAUGH
-
依托单位:
Ras signaling in C. neoformans virulence and development
-
批准号:6983384
-
项目类别:
-
资助金额:$30.08万
-
财政年份:2002
-
负责人:ANDREW ALSPAUGH
-
依托单位:
海外基金