SOLUBLE T CELL RECEPTOR STUDIES ON MHC RESTRICTION

MHC 限制的可溶性 T 细胞受体研究

基本信息

  • 批准号:
    3466765
  • 负责人:
  • 金额:
    $ 11.77万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1988
  • 资助国家:
    美国
  • 起止时间:
    1988-02-01 至 1993-01-31
  • 项目状态:
    已结题

项目摘要

We wish to analyze the stuctural basis for T cell corecognition of antigen and major histocompatibility complex (MHC) proteins, using purified, soluble forms of the T cell receptor. We will also make antibodies against particular V alpha and V beta domains of soluble T cell receptor proteins to examine possible regulation of V region expression during T cell ontogeny and during the immune response. We will produce soluble T cell receptor protein from chimeric genes containing T cell receptor V region exons and immunoglobulin constant region exons expressed in B cells under the control of immunoglobulin regulatory elements. Chimeric antibodies with T cell receptor binding sites will be purified and used in experiments to determine the specificity and binding constants (association, dissociation and equilibrium) for the T cell receptor to its ligands; peptide antigen and MHC, both individually and together. Comparison of affinities for different antigens and MHC proteins with data on the activation of the original T cell will be used to understand the role of T cell receptor affinity in T cell activation and to determine the relative contribution of antigen and MHC in normal MHC- restricted recognition of antigen. These chimeric proteins will be crystallized for x-ray diffraction determination of their crystal structure. Proteins containing individual alpha or beta chain V domains will be used to produce monoclonal antibodies reactive with these particular V regions, since such reagents have been difficult to produce with conventional immunization. These reagents will be used to examine whether there is a developmental progression in the expression of T cell receptor V regions as occurs with immunoglobulin V regions. Since many of the T cell responses to small antigenic determinants seem to utilize a very limited set of T cell receptor V regions, antibodies against suitable V regions will be used to analyze the T cell repertoire during an immune response and to modify it. Such anti-T cell receptor V region reagents may be useful in diagnosis or treatment of certain diseases.
我们希望分析T细胞共识别的结构基础

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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NICHOLAS R GASCOIGNE其他文献

NICHOLAS R GASCOIGNE的其他文献

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{{ truncateString('NICHOLAS R GASCOIGNE', 18)}}的其他基金

Themis in Type II Diabetes
忒弥斯治疗 II 型糖尿病
  • 批准号:
    8227228
  • 财政年份:
    2012
  • 资助金额:
    $ 11.77万
  • 项目类别:
Themis in Type II Diabetes
忒弥斯治疗 II 型糖尿病
  • 批准号:
    8438403
  • 财政年份:
    2012
  • 资助金额:
    $ 11.77万
  • 项目类别:
Soluble T Cell Receptor Studies on MHC Restriction
MHC 限制的可溶性 T 细胞受体研究
  • 批准号:
    8075341
  • 财政年份:
    2010
  • 资助金额:
    $ 11.77万
  • 项目类别:
A novel protein regulating thymocyte development
调节胸腺细胞发育的新型蛋白质
  • 批准号:
    7842644
  • 财政年份:
    2009
  • 资助金额:
    $ 11.77万
  • 项目类别:
A novel protein regulating thymocyte development
调节胸腺细胞发育的新型蛋白质
  • 批准号:
    7532691
  • 财政年份:
    2009
  • 资助金额:
    $ 11.77万
  • 项目类别:
Themis Regulation of Thymocyte Selection
Themis 对胸腺细胞选择的调节
  • 批准号:
    8337944
  • 财政年份:
    2009
  • 资助金额:
    $ 11.77万
  • 项目类别:
Soluble T Cell Receptor Studies on MHC Restriction
MHC 限制的可溶性 T 细胞受体研究
  • 批准号:
    7929243
  • 财政年份:
    2009
  • 资助金额:
    $ 11.77万
  • 项目类别:
Molecular Interactions in the Aging Immunological Synapse
衰老免疫突触中的分子相互作用
  • 批准号:
    7333193
  • 财政年份:
    2007
  • 资助金额:
    $ 11.77万
  • 项目类别:
Molecular Interactions in the Aging Immunological Synapse
衰老免疫突触中的分子相互作用
  • 批准号:
    7479289
  • 财政年份:
    2007
  • 资助金额:
    $ 11.77万
  • 项目类别:
Leica TCSSP2RS two-photon microscope for in vivo imaging
用于活体成像的 Leica TCSP2RS 双光子显微镜
  • 批准号:
    7050299
  • 财政年份:
    2006
  • 资助金额:
    $ 11.77万
  • 项目类别:

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