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
- 来源:
- 关键词:B lymphocyte RNA splicing T cell receptor T lymphocyte X ray crystallography antibody specificity antigens antireceptor antibody cell cell interaction chemical binding fusion gene gene expression genetic regulation histocompatibility antigens immunofluorescence technique immunoglobulin genes immunoregulation laboratory mouse laboratory rat leukopoiesis major histocompatibility complex monoclonal antibody nucleic acid hybridization secretion tissue /cell culture transfection
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
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{{ truncateString('NICHOLAS R GASCOIGNE', 18)}}的其他基金
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:
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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