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Complete amino acid sequence of heavy chain variable regions derived from two monoclonal anti-p-azophenylarsonate antibodies of BALB/c mice expressing the major cross-reactive idiotype of the A/J strain

机译:来自表达A / J株主要交叉反应性独特型的BALB / c小鼠的两种单克隆抗对偶氮苯基砷酸酯单克隆抗体的重链可变区的完整氨基酸序列

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摘要

The primary structure of A/J anti-p-azophenylarsonate (anti-Ars) antibodies expressing the major A-strain cross-reactive idiotype (CRIA) has provided important insights into issues of antibody diversity and the molecular basis of idiotypy in this important model system. Until recently, this idiotype was thought to be rarely, if ever, expressed in BALB/c mice. Indeed, it has been reported that BALB/c mice lack the heavy chain variable segment (VH) gene that is utilized by the entire family of anti-Ars antibodies expressing the A/J CRI. Recently, however, it has been possible to elicit CRIA+, Ars binding antibodies in the BALB/c strain by immunizing first with anti-CRI and then with antigen. Such BALB/c, CRIA+ anti-Ars antibodies can be induced occasionally with antigen alone. VH region amino acid sequences are described for two CRIA+ hybridoma products derived from BALB/c mice. While remarkably similar to each other, their VH segments (1-98) differ from the VH segments of A/J CRIA+, anti-Ars antibodies in over 40 positions. Rather than the usual JH2 gene segment used by most A/J CRIA+ anti-Ars antibodies, one BALB/c CRIA+ hybridoma utilizes a JH1 gene segment, while the other uses a JH4. However, the D segments of both of the BALB/c antibodies are remarkably homologous to the D segments of several A/J CRIA+ antibodies sequenced previously, as are the amino terminal amino acid sequences of their light chains. These data imply that BALB/c mice express the A/J CRIA by producing antibodies with very similar, if not identical, light chain and heavy chain D segments, but in the context of different VH and JH gene segments than their A/J counterparts. The results document that molecules that share serologic specificities can have vastly different primary structures.
机译:表达主要A株交叉反应独特型(CRIA)的A / J抗对偶氮苯基砷酸酯(anti-Ars)抗体的一级结构为该重要模型中的抗体多样性和独特性的分子基础提供了重要见解系统。直到最近,人们仍认为这种独特型很少在BALB / c小鼠中表达。实际上,据报道,BALB / c小鼠缺乏表达A / J CRI的整个抗Ars抗体家族所利用的重链可变节(VH)基因。但是,最近有可能通过先用抗CRI然后再用抗原免疫在BALB / c菌株中引发CRIA +,与Ars结合的抗体。这种BALB / c,CRIA +抗Ars抗体有时可以单独用抗原诱导。描述了来自BALB / c小鼠的两种CRIA +杂交瘤产物的VH区氨基酸序列。虽然彼此非常相似,但它们的VH区段(1-98)与A / J CRIA +抗Ars抗体的VH区段在40多个位置上有所不同。一种BALB / c CRIA +杂交瘤利用JH1基因区段,而另一种使用JH4,而不是大多数A / J CRIA +抗Ars抗体所使用的通常的JH2基因区段。但是,两种BALB / c抗体的D区段与先前测序的几种A / J CRIA +抗体的D区段均具有显着同源性,其轻链的氨基末端氨基酸序列也是如此。这些数据表明,BALB / c小鼠通过产生具有非常相似(如果不是相同的话)轻链和重链D片段的抗体表达A / J CRIA,但是在与它们的A / J对应物不同的VH和JH基因片段的背景下。结果表明,具有血清学特异性的分子可以具有截然不同的一级结构。

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