Murine V kappa 25 and V kappa 27 amino-acid sequences of C57B1/6 origin: monoclonal antibodies 17S29.1 and 22S25.1 specific for the group A-streptococcal polysaccharide.

R Aebersold, H Herbst, T Grütter, J Y Chang, D G Braun
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Abstract

Antibodies 17S29.1 and 22S25.1 are monoclonal, hybridoma-derived gamma 3 kappa murine immunoglobulins with specificity for N-acetyl-glucosamine beta 1----3-linked to the L-rhamnose backbone structure, the immunodeterminant of the streptococcal Group A polysaccharide. The VL 17S29.1 amino-acid sequence is the third complete one reported from an antibody with this specificity, the second fully determined V kappa 25 structure and the first complete V kappa sequence of C57B1/6 origin derived from a carbohydrate-specific antibody. VL22S25.1 is a member of the V kappa 27 isotype of murine immunoglobulin VL regions. V kappa 17S29.1 and the determined part of the V kappa 22S25.1 sequence are compared to the previously described V kappa regions of streptococcal Group A polysaccharide-specific antibodies and to 12 selected partial and complete V kappa regions of antibodies with other specificities, predominantly to carbohydrate antigens. Both V kappa 17S29.1 and V kappa 22S25.1 increase the variability of known murine V kappa regions. They are the most homologous to the other V kappa regions derived from antibodies with streptococcal Group A polysaccharide specificity and share with them the amino-acid residue Arg74, so far characteristic for V kappa regions from antibodies with this specificity. The analysis of groups of independently expressed, highly homologous V kappa regions, namely V kappa 17S29.1 and V kappa 2S1.3 as one and V kappa 7S34.1 and V kappa 22S25.1 as a second group, offers the possibility of estimating the minimal number of V kappa germline genes involved in the immune response to the structurally defined streptococcal Group A polysaccharide antigen.(ABSTRACT TRUNCATED AT 250 WORDS)

小鼠C57B1/6来源的V kappa 25和V kappa 27氨基酸序列:a组链球菌多糖特异性单克隆抗体17S29.1和22S25.1。
抗体17S29.1和22S25.1是单克隆的杂交瘤来源的γ -3 κ pa小鼠免疫球蛋白,特异性为n -乙酰氨基葡萄糖β 1----3-连接到l-鼠李糖骨架结构,该结构是链球菌A群多糖的免疫决定因素。VL 17S29.1氨基酸序列是报道的第三个完整的来自该特异性抗体的序列,第二个完全确定的V kappa 25结构和第一个完整的源自碳水化合物特异性抗体的C57B1/6的V kappa序列。VL22S25.1是小鼠免疫球蛋白VL区V kappa 27同型的成员。将V kappa 17S29.1和V kappa 22S25.1序列的确定部分与先前描述的链球菌A组多糖特异性抗体的V kappa区域以及与其他特异性抗体(主要针对碳水化合物抗原)的12个选定的部分和完全V kappa区域进行比较。V kappa 17S29.1和V kappa 22S25.1都增加了已知小鼠V kappa区的变异性。它们与具有链球菌A群多糖特异性的抗体衍生的其他V kappa区最同源,并与它们共享氨基酸残基Arg74,这是迄今为止具有该特异性的抗体衍生的V kappa区的特征。通过分析独立表达的高度同源的V kappa区,即V kappa 17S29.1和V kappa 2S1.3为一组,V kappa 7S34.1和V kappa 22S25.1为第二组,可以估计参与对结构确定的链球菌a组多糖抗原免疫应答的V kappa种系基因的最小数量。(摘要删节250字)
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