The δ- and ε-chains of the human T3/T-cell receptor complex are distinct polypeptides
The δ- and ε-chains of the human T3/T-cell receptor complex are distinct polypeptides
复制标题
人类 T3/T 细胞受体复合物的 δ 链和 ε 链是不同的多肽
作者:
J. Borst;J. Coligan;H. Oettgen;S. Pessano;R. Malin;C. Terhorst
The T3/T-cell receptor complex on the surface of human thymus-derived lymphocytes consists of four glycoproteins: the α-chain of relative molecular mass (Mr) 40,000–50,000 (40–50K), the β-chain (37–45K); the γ-chain (25K) and the δ-chain (20K)1–3. The T3 α- and β-chains have been identified as clonotypic T-cell receptors3–7, but functionally the T3/T-cell receptor chains seem to form a single complex: monoclonal antibodies directed at the 20K T3 components are mitogenic for normal human T lymphocytes8,9 and, at higher concentrations, anti-clonotypic and anti-20K reagents block T-cell function4,10. Recently, Zanders et al.11 showed that incubation of human T-helper clones with high concentrations of antigen abolishes antigen-specific proliferation and induces disappearance of T3 from the cell surface. Thus, the T3/T-cell receptor complex consists of two variable subunits, the T3 α- and β-chains, which interact with antigen and the monomorphic 20K/25K T3 chains. Recently, the existence of a fifth polypeptide chain, the unglycosylated T3 ε-chain, has been postulated12,13. Here we confirm that a 20K ε-chain does exist. The T3 ε-chain differs from the T3 δ-chain in primary structure as judged by N-terminal amino acid sequencing, peptide mapping and immuno-blotting with anti-T3-δ and anti-T3-ε antibodies. Treatment with endoglycosidase F revealed two nonglycosylated T3 δ polypeptide backbone chains (16K and 14K) with identical amino termini. Together with previous pulse-chase experiments2 this observation suggests that the 14K T3 polypeptide is derived from the 16K T3 precursor by proteolytic processing near the C-terminus of the molecule.
登录
查看更多内容
DOI:
--
发表时间:
1984
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Snow,PM;Keizer,G;Coligan,JE;Terhorst,C
通讯作者:
Terhorst,C
DOI:
10.1073/pnas.80.13.4104
发表时间:
1983
影响因子:
11.1
作者:
Reinherz,EL;Meuer,SC;Fitzgerald,KA;Hussey,RE;Hodgdon,JC;Acuto,O;Schlossman,SF
通讯作者:
Schlossman,SF
DOI:
10.1016/s0021-9258(18)32549-3
发表时间:
1983-04
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Jannie Borst;Stephen Alexander;John Elder;Cox TerhorstSn
通讯作者:
Jannie Borst;Stephen Alexander;John Elder;Cox TerhorstSn
影响因子:
2.9
作者:
Adair,WS
通讯作者:
Adair,WS
影响因子:
4.4
作者:
James P. Allison;Bradley W. McIntyre;D. Bloch
通讯作者:
James P. Allison;Bradley W. McIntyre;D. Bloch