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中文摘要
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描述(由申请人提供):干扰素γ(IFN-gamma)在免疫系统的调节中发挥着至关重要的作用,并且几乎对所有组织都有活性。其作用由作为本申请主题的其受体介导。我们以前确定了两条链(IFN-γ R1和IFN-γ R2),这是受体活性所必需的。目前的建议侧重于在存在和不存在配体的情况下,在活细胞中IFN-γ受体复合物的链的结构。针对这些目标的具体目的是:确定是否所有IFN-γ受体链预结合; Jak激酶在预组装中的作用;确定受体链上用于预组装的位点; Stat 1在细胞内结构域运动中的作用;确定配体结合后受体结构变化的动力学;分析下游信号传导组分与受体复合物的动力学和相互作用;确定受体的位点,其用作IFN-γ和IFN-α受体复合物之间的串扰位点。受体链的构型将通过活细胞中的荧光共振能量转移来研究。由于IFN-γ在细胞和免疫功能中起着关键作用,因此了解其作用的所有这些方面将导致更好的策略来攻击各种疾病,如癌症,传染病和自身免疫性疾病。该技术的进一步应用将导致用于高通量筛选和实时鉴定活细胞中蛋白质-蛋白质相互作用的新的快速方法。
英文摘要
DESCRIPTION (provided by applicant): Interferon gamma (IFN-gamma) plays a crucial role in regulation of the immune system and is active on virtually all tissues. Its actions are mediated by its receptor that is the subject of this application. We previously identified two chains (IFN-gammaR1 and IFN-gammaR2) that are required for receptor activity. The current proposal focuses on the structure of the chains of the IFN-gamma receptor complex in live cells in the presence and absence of ligand. The specific aims directed to these goals are: to determine if all the IFN-gamma, receptor chains preassociated; the role of the Jak kinases in preassembly; determination of the sites on the receptor chains for preassembly; role of Stat1 in movement of the intracellular domains; determination of the kinetics of change in receptor structure after ligand binding; analysis of the kinetics and interactions of the downstream signaling components with the receptor complex; determine the sites of the receptor that serve as sites for cross-talk between the IFN-gamma and IFN-alpha receptor complexes. The configuration of the receptor chains will be studied by fluorescence resonance energy transfer in live cells. Because IFN-gamma plays a critical role in cellular and immune function, understanding all these aspects of its action will lead to better strategies to attack a variety of diseases such as cancers, and infectious and autoimmune diseases. Further application of this technology should lead to new rapid methods for high throughput screening and for identifying protein-protein interactions in live cells in real-time.
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TIME-RESOLVED STUDY OF PROTEIN:PROTEIN INTERACTIONS IN SINGLE CELLS
  • 批准号:
    7955432
  • 项目类别:
  • 资助金额:
    $0.48万
  • 财政年份:
    2009
  • 负责人:
    SIDNEY PESTKA
  • 依托单位:
Role of mRNA Decay in the Immune System
TIME-RESOLVED STUDY OF PROTEIN:PROTEIN INTERACTIONS IN SINGLE CELLS
  • 批准号:
    7723841
  • 项目类别:
  • 资助金额:
    $0.77万
  • 财政年份:
    2008
  • 负责人:
    SIDNEY PESTKA
  • 依托单位:
TIME-RESOLVED STUDY OF PROTEIN:PROTEIN INTERACTIONS IN SINGLE CELLS
  • 批准号:
    7598435
  • 项目类别:
  • 资助金额:
    $0.48万
  • 财政年份:
    2007
  • 负责人:
    SIDNEY PESTKA
  • 依托单位:
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