MOUSE T CELL RECEPTORS SPECIFIC FOR VESICULAR STOMATITIS VIRUS & HIV CD4 STRUCT
水泡性口炎病毒特异性小鼠 T 细胞受体
基本信息
- 批准号:6346394
- 负责人:
- 金额:$ 5.83万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2000
- 资助国家:美国
- 起止时间:2000-09-01 至 2001-08-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
To solve the three dimensional structures of multiple murine T
cell receptors specific for a viral octapeptide (VSV8) bound to the K
b MHC class I molecule
T cells recognize cell-associated pathogens of viral, bacteria[ or
fungal origin as well as tumor antigens through a unique molecule
termed the T cell receptor (TCR). The TCR complex consists of
multiple transmembrane chains on the surface of T lymphocytes',". The
disulfide-linked a-P heterodimer is a clonally unique component that
possesses a recognition site for antigen in the context of the major
histocompatibility complex (MHC), while the invariant CD3 components
(y, 6, e, and Q are involved in signal transduction. Because of the
intimate membrane association of this complex, study of the molecular
features of TCR recognition necessarily have been indirect.
Recent efforts to understand the nature of this recognition process
have focused on structural studies of the system. It has been known
for a few years that both class I and class 11 MHC molecules, despite
the very different chemical compositions of the two subunits, have the
same topologic structure"-s. in particular, the way MHC molecules
present the antigenic peptide is similar. A short antigenic peptide
(8-10 residues for class I and >1 2 residues for class 11) lies in a
large groove at the top of the MHC molecule. This groove is composed
of eight strands of anti-parallel P-sheet as a floor, and two
anti-parallel a-helices as side walls. In class I MHC molecules, the
whole groove is formed by domain al and a2 from the same a chain; in
class 11 MHC molecules, the groove is formed by domain al, and 01 from
two different chains (a and 0). Structural details of how peptides
bind with high affinity to these MHC molecules have been well
characterized.
多个小鼠T细胞的三维结构解析
与K蛋白结合的病毒八肽(VSV8)的细胞受体
B MHC I类分子
T细胞识别病毒、细菌的细胞相关病原体[或
真菌起源和肿瘤抗原通过一种独特的分子
被称为T细胞受体(TCR)。TCR综合体包括
T淋巴细胞表面的多个跨膜链。
二硫键连接的α-P杂二聚体是一种克隆性独特的成分,它
在重大疾病的背景下拥有抗原的识别位置
组织相容性复合体(MHC),而不变的CD3成分
(y、6、e和q参与信号转导。因为
这种复合体的紧密膜缔合,分子的研究
TCR识别的特征必然是间接的。
最近为了解这一承认过程的性质所作的努力
都把重点放在了系统的结构研究上。众所周知,
几年来,I类和11类MHC分子,尽管
这两个亚基的化学成分非常不同,
相同的拓扑结构“-S,尤其是MHC分子
目前的抗原肽是相似的。一种短的抗原肽
(第I类为8-10个残基,第11类为12个残基)位于
MHC分子顶部的大凹槽。这条沟槽是由
八股反平行P片作为地板,两股
反平行的a型螺旋作为侧壁。在I类MHC分子中,
整个凹槽由来自相同a链的区域a1和a2形成;
11类MHC分子,凹槽由结构域al和01形成
两个不同的链(a和0)。多肽的结构细节
与这些MHC分子具有高亲和力的结合一直很好
特色化的。
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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{{ truncateString('ELLIS L REINHERZ', 18)}}的其他基金
A precision tumor neoantigen identification pipeline for cytotoxic T-lymphocyte-based cancer immunotherapies
用于基于细胞毒性 T 淋巴细胞的癌症免疫疗法的精准肿瘤新抗原识别流程
- 批准号:
10581488 - 财政年份:2022
- 资助金额:
$ 5.83万 - 项目类别:
A precision tumor neoantigen identification pipeline for cytotoxic T-lymphocyte-based cancer immunotherapies
用于基于细胞毒性 T 淋巴细胞的癌症免疫疗法的精准肿瘤新抗原识别流程
- 批准号:
10332251 - 财政年份:2022
- 资助金额:
$ 5.83万 - 项目类别:
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