NeuGc-containing神经节苷脂家族中编码AB1和γ型AB2抗体的可变区免疫遗传学分析。

Alexis Pérez, Josefa Lombardero, Cristina Mateo, G. Mustelier, M. Alfonso, A. Vázquez, Rolando Pérez
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引用次数: 28

摘要

克隆并测序了针对neugc -神经节苷的小鼠单克隆抗体(MAb) P3的可变区和针对P3 MAb的两个抗独特型MAb。P3是由V(H)Q52和V(kappa)19家族基因编码的种系抗体。对重链CDR3 (H-CDR3)核苷酸的分析显示,存在一个广泛的3' N区域,该区域包含该CDR近50%的核苷酸。此外,对该单抗的h - cdr的氨基酸序列分析显示,存在三个精氨酸,其中两个存在于H-CDR3中,它们可能参与P3单抗与其神经节苷上的电负性表位的相互作用。抗独特型1E10似乎在P3单抗上定义了一个“调节”独特型(它诱导Id+ Ab3),代表了一个属于V(H)J558和V(kappa)10基因家族的种系Ab2。相反,抗独特型3B11是一种广泛突变的抗体,属于V(H)3660和V(kappa)4/5基因家族,在P3 MAb上定义了一个“私有”独特型。即使不同的V基因参与了1E10和3B11单克隆抗体的可变区域,它们在H-CDR3中共享一个酸性基序E/D-D-Y/D-Y-D,这表明这两个Ab2s都识别Ab1上的副正残基。因此,来自Ab1和Ab2的H-CDR3的互补静电相互作用可能为理解识别糖酰化神经节苷抗原的V区产生γ型抗独特型抗体的分子基础提供了线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunogenetic analysis of variable regions encoding AB1 and gamma-type AB2 antibodies from the NeuGc-containing ganglioside family.
The variable regions from P3, a murine monoclonal antibody (MAb) against NeuGc-containing gangliosides, and two anti-idiotype MAbs directed to P3 MAb were cloned and sequenced. Comparisons with previously reported sequences showed that P3 is a germline antibody encoded by genes from the V(H)Q52 and V(kappa)19 families. Analysis of nucleotides at the heavy chain CDR3 (H-CDR3) showed the presence of an extensive 3' N region that contains almost 50% of the nucleotides of this CDR. In addition, amino acid sequence analysis of the H-CDRs of this MAb revealed the presence of three arginines, two of which are present in the H-CDR3, that could be involved in the interaction of P3 MAb with its electronegative epitope on gangliosides. Anti-idiotype 1E10, which seems to define a "regulatory" idiotope on P3 MAb (it induces Id+ Ab3), represents a germline Ab2 that belongs to the V(H)J558 and V(kappa)10 gene families. By contrary, the anti-idiotype 3B11 is an extensively mutated antibody that belongs to the V(H)3660 and V(kappa)4/5 gene families, defining a "private" idiotope on P3 MAb. Even when different V genes contribute to the variable regions of 1E10 and 3B11 MAbs, they share an acidic motif E/D-D-Y/D-Y-D in H-CDR3, suggesting that both Ab2s recognize paratope positive residues on the Ab1. Therefore, complementary electrostatic interactions involving H-CDR3 from both Ab1 and Ab2, might provide a clue to understand the molecular basis for the generation of gamma-type anti-idiotype antibodies to V regions recognizing glycolylated ganglioside antigens.
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来源期刊
Hybridoma
Hybridoma 医学-免疫学
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