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来自一只携带主要砷酸盐独特型的A/J小鼠抗原非结合单克隆抗体的重链可变区的完整氨基酸序列。

Complete amino acid sequence of the heavy-chain variable region from an A/J mouse antigen-nonbinding monoclonal antibody bearing the predominant arsonate idiotype.

作者信息

Smith J A, Margolies M N

出版信息

Biochemistry. 1984 Sep 25;23(20):4726-32. doi: 10.1021/bi00315a031.

Abstract

The 1F6 hybridoma protein, exhibiting the predominant cross-reactive idiotype (CRI) associated with the immune response to p-azophenylarsonate in A/J mice but failing to bind the hapten arsonate, was elicited following immunization with rat anti-CRI [Wysocki, L.J., & Sato, V. (1981) Eur. J. Immunol. 11, 832-839]. The dissociation of idiotype and antigen binding in this hybridoma provides an opportunity to determine structural features involved in antigen binding and idiotypic sites. The complete heavy-chain variable region (VH) amino acid sequence was obtained by automated Edman degradation of the intact chain and fragments due to CNBr cleavage, trypsin digestion, mild acid hydrolysis, and carboxypeptidase A digestion of a CNBr fragment. Comparison of the CRI+ arsonate-nonbinding 1F6 sequence with the CRI+ germ-line VH gene sequence reveals that the 1F6 heavy chain differs from the germ-line-encoded amino acid sequence at seven positions within VH [Siekevitz, M., Gefter, M. L., Brodeur, P., Riblet, R., & Marshak-Rothstein, A. (1982) Eur. J. Immunol. 12, 1023-1032]. The 1F6 VH appears to arise from the CRI+ germ-line VH by somatic mutation at at least seven amino acid residues, each of which could be due to a single nucleotide base change. The diversity (D) gene-encoded segment of 1F6 is similar to that of the CRI+ antigen-binding hybridoma 36-65 except for two amino acid substitutions. Further, the idiotype (CRI) is preserved despite use of a JH4 gene segment in 1F6 as compared to JH2 in all CRI+ arsonate-binding hybridomas examined to date.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

1F6杂交瘤蛋白表现出与A/J小鼠对对氨基苯胂酸盐免疫反应相关的主要交叉反应独特型(CRI),但不能结合半抗原胂酸盐,在用大鼠抗CRI免疫后产生[Wysocki, L.J., & Sato, V. (1981) Eur. J. Immunol. 11, 832 - 839]。这种杂交瘤中独特型与抗原结合的解离提供了一个机会来确定参与抗原结合和独特型位点的结构特征。完整重链可变区(VH)氨基酸序列是通过对完整链以及由于CNBr裂解、胰蛋白酶消化、温和酸水解和对一个CNBr片段进行羧肽酶A消化产生的片段进行自动Edman降解获得的。将CRI + 胂酸盐非结合性1F6序列与CRI + 种系VH基因序列进行比较,发现1F6重链在VH内的七个位置与种系编码的氨基酸序列不同[Siekevitz, M., Gefter, M. L., Brodeur, P., Riblet, R., & Marshak-Rothstein, A. (1982) Eur. J. Immunol. 12, 1023 - 1032]。1F6 VH似乎通过至少七个氨基酸残基的体细胞突变从CRI + 种系VH产生,每个氨基酸残基的变化可能是由于单个核苷酸碱基改变。1F6的多样性(D)基因编码片段与CRI + 抗原结合杂交瘤36 - 65的相似,只是有两个氨基酸替换。此外,尽管1F6使用的是JH4基因片段,而迄今为止检测的所有CRI + 胂酸盐结合杂交瘤使用的是JH2基因片段,但独特型(CRI)得以保留。(摘要截短于250字)

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