Structure Studies on Proteins that Modulate IL-10 Action
Structure Studies on Proteins that Modulate IL-10 Action
批准号:
7263533
负责人:
MARK R WALTER
金额:
$36.25万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-04-01 至 2012-04-30
关键词:
AffinityAutoimmune DiseasesB lymphoid malignancyB-LymphocytesBindingBinding SitesBiologicalBiologyCell Surface ReceptorsCell surfaceComplementComplexComputer SimulationCongenital AbnormalityCrystallographyCytomegalovirusCytomegalovirus InfectionsDataEmployee StrikesExhibitsFamilyFluorescence Resonance Energy TransferFundingGenomeGoalsGrowth FactorHomologous GeneHumanHuman Herpesvirus 4IL10RB geneImmune responseInfectionInflammatory ResponseInterferonsInterleukin-10KineticsMeasurableMeasuresMediatingMethodsNMR SpectroscopyPropertyProtein DynamicsProteinsResearch PersonnelShapesSignal TransductionSite-Directed MutagenesisSolutionsStructural ModelsStructureSurface Plasmon ResonanceSystemTechniquesTherapeuticViralVirusVirus DiseasesX ray diffraction analysisX ray spectroscopyX-Ray Crystallographyautocrinebasecell typecytokinedefined contributiondesignimprovedinterleukin 20interleukin-10 receptorinterleukin-22metaplastic cell transformationmutantprogramsreceptorreceptor bindingresponsethree-dimensional modeling
中文摘要
描述(由申请人提供):IL-10是一种调节复杂免疫应答的多功能细胞因子。它的正常功能是保护宿主免受不受控制的炎症反应。然而,IL-10也被认为是几种B细胞恶性肿瘤中的自分泌生长因子,并刺激B细胞介导的自身免疫性疾病。IL-10的正常和病理功能是通过IL-10受体接合和组装成具有信号传导能力的IL-10/IL-10 R1/IL-10 R2复合物来启动的。除了细胞IL-10(cIL-10)之外,爱泼斯坦巴尔病毒(EBV)和巨细胞病毒(CMV)在其基因组中具有激活IL-10信号传导复合物的病毒IL-10模拟物(ebvIL-10和cmvIL-10),导致重叠和不同的生物学特性。在过去的资助期间,我们确定了与高亲和力IL-10 R1链结合的clL-10、cmvIL-10和ebvIL-10的晶体结构。在这个提议中,我们将使用表面等离子体共振,定点诱变,NMR光谱,X射线晶体学,和FRET方法来研究细胞和病毒IL-10受体的相互作用。这些研究将通过分析细胞IL-10同系物IL- 22和IL-20来补充。该提案的长期目标是推导出IL-10家族信号传导的定量结构/计算模型,该模型可以解释细胞和病毒IL-10如何形成免疫应答,并允许合理设计细胞因子疗法。
英文摘要
DESCRIPTION (provided by applicant): IL-10 is a multifunctional cytokine that regulates complex immune responses. Its normal function is to protect the host from uncontrolled inflammatory responses. However, IL-10 has also been implicated as an autocrine growth factor in several B-cell malignancies and stimulates B-cell mediated autoimmune disease. The normal and pathological functions of IL-10 are initiated by IL-10 receptor engagement and assembly into a signaling competent IL-10/IL-10R1/IL-10R2 complex. In addition to cellular IL-10 (clL-10), Epstein Barr virus (EBV) and cytomegalovirus (CMV) harbor viral IL-10 mimics (ebvlL-10 and cmvlL-10) in their genomes that activate the IL-10 signaling complex, resulting in overlapping and distinct biological properties. In the past funding period, we determined crystal structures of clL-10, cmvlL-10, and ebvlL-10 bound to the high affinity IL-10R1 chain. In this proposal we will use surface plasmon resonance, site-directed mutagenesis, NMR spectroscopy, X-ray crystallography, and FRET methods to study cellular and viral IL-10 receptor interactions. These studies will be complemented by the analysis of the cellular IL-10 homologs IL- 22 and IL-20. The long term goal of this proposal is to derive a quantitative structural/computational model of IL-10 family signaling that might explain how cellular and viral IL-10s shape immune responses and allow the rational design of cytokine therapeutics.
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会议论文
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资助金额:$0.03万
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财政年份:2011
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依托单位:
STRUCTURE OF RECEPTOR COMPLEXES
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资助金额:$1.1万
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资助金额:$0.02万
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Structure Studies on Proteins that Modulate IL-10 Action
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资助金额:$14.76万
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