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一个克隆的独特型级联的分子特征分析,该级联包含对人癌胚抗原具有特异性的网络抗原决定簇。

Molecular characterization of a cloned idiotypic cascade containing a network antigenic determinant specific for the human carcinoembryonic antigen.

作者信息

Gaida F J, Pieper D, Roder U W, Shively J E, Wagener C, Neumaier M

机构信息

Department of Clinical Chemistry, Universitätskrankenhaus Eppendorf, Hamburg, Germany.

出版信息

J Biol Chem. 1993 Jul 5;268(19):14138-45.

PMID:7686150
Abstract

The monoclonal anti-idiotypic antibody (maId) 6G6.C4, directed against the carcinoembryonic antigen (CEA)-specific T84.66 immunoglobulin, was recently shown to act as a surrogate antigen for CEA in experimental animals. In this report, we have extended our studies. 1) The kinetics of complex formation in this CEA-specific idiotypic cascade were investigated using Biosensor technology. 2) Bacterial expression studies show that the mimicked epitope can be delimited to the A3 domain of CEA. 3) We cloned and characterized the genes coding for maId 6G6.C4. 4) Comparison of this epitope-bearing domain with the hypervariable region sequences of 6G6.C4 yields substantial amino acid similarity. Sequence homology between maId 6G6.C4 and anti-CEA antibodies binding to the T84.66 epitope led us to investigate the interaction of maId 6G6.C4 and CEA. Surprisingly, 6G6.C4 specifically binds to CEA but not CEA-related antigens in Western blots. 6G6.C4 and T84.66 recognize different epitopes on CEA. Our results suggest that the T84.66 epitope functionally mimicked by maId 6G6.C4 may be involved in the homophilic binding between CEA molecules, and that heterophilic interactions in the CEA-family are mediated by different binding sites. A model for the intermolecular adhesion of CEA is presented.

摘要

针对癌胚抗原(CEA)特异性T84.66免疫球蛋白的单克隆抗独特型抗体(maId)6G6.C4,最近在实验动物中被证明可作为CEA的替代抗原。在本报告中,我们扩展了研究。1)使用生物传感器技术研究了该CEA特异性独特型级联中复合物形成的动力学。2)细菌表达研究表明,模拟表位可限定于CEA的A3结构域。3)我们克隆并鉴定了编码maId 6G6.C4的基因。4)将这个带有表位的结构域与6G6.C4的高变区序列进行比较,发现氨基酸有很大的相似性。maId 6G6.C4与结合T84.66表位的抗CEA抗体之间的序列同源性,促使我们研究maId 6G6.C4与CEA的相互作用。令人惊讶的是,在蛋白质印迹中,6G6.C4特异性结合CEA而非CEA相关抗原。6G6.C4和T84.66识别CEA上不同的表位。我们的结果表明,maId 6G6.C4功能模拟的T84.66表位可能参与CEA分子之间的嗜同性结合,并且CEA家族中的异嗜性相互作用是由不同的结合位点介导的。本文提出了一个CEA分子间粘附的模型。

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