Ruf J, Tonnelle C, Rocca-Serra J, Moinier D, Pierres M, Ju S T, Dorf M E, Thèze J, Fougereau M
Proc Natl Acad Sci U S A. 1983 May;80(10):3040-4. doi: 10.1073/pnas.80.10.3040.
NH2-terminal amino acid sequences of heavy and light chains of seven poly(Glu60Ala30Tyr10) (GAT) specific hybridoma products derived from DBA/2 and (DBA/2 X BALB/c)F1 hybrid mice and those of BALB/B polyclonal antibodies have been determined over the first 40 residues. Comparison of these sequences with those of nine other GAT or poly(Glu60Ala40) (GA) specific hybridoma products previously reported allowed the following conclusions. (i) Sequences of hybridoma H and L chains are present in the pool of polyclonal antibodies. (ii) The public CGAT (or pGAT) idiotypic specificities are strictly confined to antibodies exhibiting limited heterogeneity with regard to both the variable heavy (VH) and the variable kappa (V kappa) sequences that may be accounted for by one and two germ-line genes, respectively. (iii) The public idiotypic specificities GA-1, expressed by some anti-GAT and most anti-GA antibodies, make use of the same (or similar) VH germ-line genes as the CGAT or pGAT antibodies but possess a distinctive V kappa sequence. (iv) Antibodies expressing neither of the alternative public specificities mentioned above appear to be more heterogeneous and express VH and V kappa sequences that were found to differ from the basic structures defining the CGAT (pGAT) or GA-1 correlates. It is concluded that CGAT (or pGAT) and GA-1 public idiotypic specificities are germ-line markers of both VH and V kappa regions, an observation in agreement with previously reported serological data.
已测定了来自DBA/2和(DBA/2×BALB/c)F1杂交小鼠的7种聚(Glu60Ala30Tyr10)(GAT)特异性杂交瘤产物以及BALB/B多克隆抗体的重链和轻链的N端氨基酸序列,涵盖前40个残基。将这些序列与先前报道的其他9种GAT或聚(Glu60Ala40)(GA)特异性杂交瘤产物的序列进行比较,得出以下结论。(i)杂交瘤重链和轻链序列存在于多克隆抗体库中。(ii)公共CGAT(或pGAT)独特型特异性严格局限于在可变重链(VH)和可变κ链(Vκ)序列方面表现出有限异质性的抗体,这可能分别由一个和两个种系基因引起。(iii)一些抗GAT和大多数抗GA抗体所表达的公共独特型特异性GA-1,与CGAT或pGAT抗体利用相同(或相似)的VH种系基因,但具有独特的Vκ序列。(iv)既不表达上述两种替代公共特异性的抗体似乎更加异质,并且表达的VH和Vκ序列与定义CGAT(pGAT)或GA-1相关性的基本结构不同。结论是,CGAT(或pGAT)和GA-1公共独特型特异性是VH和Vκ区域的种系标记,这一观察结果与先前报道的血清学数据一致。