Tonnelle C, Rocca-Serra J, Moulin A, Moinier D, Fougereau M
J Exp Med. 1983 Nov 1;158(5):1415-27. doi: 10.1084/jem.158.5.1415.
A large proportion of (Glu60 Ala30 Tyr10)n (GAT)-specific antibodies expresses public idiotypic specificities, termed CGAT (or pGAT), that require the presence of both the heavy and the light chains in order to be expressed. We report in this paper the complete sequence of eight V kappa regions pertaining to eight anti-GAT monoclonal antibodies derived from three strains of mice: BALB/c, DBA/2, and C57BL/6. The methodology used a combination of NH2-terminal amino acid and mRNA nucleotide sequencing. All eight sequences analyzed, although highly homologous and all pertaining to the same V kappa 1 subgroup, allowed definition of three germline genes that are likely to be present in all three strains of mice and also in NZB. It seems likely, however, that any given strain may not necessarily use all three genes for making anti-GAT antibodies. The search for structural correlates of idiotypes could not be framed in a simple picture, but our data suggest that similar idiotopes may result from different interacting primary structures, leading to structural homologies that should be visualized at three-dimensional level.
很大一部分(Glu60 Ala30 Tyr10)n(GAT)特异性抗体表达共有独特型特异性,称为CGAT(或pGAT),其表达需要重链和轻链同时存在。我们在本文中报告了来自三株小鼠(BALB/c、DBA/2和C57BL/6)的八种抗GAT单克隆抗体的八个Vκ区域的完整序列。所使用的方法结合了氨基末端氨基酸测序和mRNA核苷酸测序。分析的所有八个序列,尽管高度同源且都属于同一个Vκ1亚组,但确定了三个可能存在于所有三株小鼠以及NZB中的种系基因。然而,任何给定的品系不一定使用所有三个基因来产生抗GAT抗体。对独特型结构相关性的研究无法用简单的情况来概括,但我们的数据表明,相似的独特位可能由不同相互作用的一级结构产生,从而导致应在三维水平上可视化的结构同源性。