Suppr超能文献

[抗独特型抗体与天然催化活性抗体]

[Anti-idiotypic and natural catalytically active antibodies].

作者信息

Shuster A M, Gololobov G V, Kvashuk O A, Gabibov A G

出版信息

Mol Biol (Mosk). 1991 May-Jun;25(3):593-602.

PMID:1658616
Abstract

The principal existence of natural catalytic antibodies in the autoimmune sera is discussed. In the course of the autoimmune process, the induction of antiidiotypic antibodies against topoisomerase I has been shown in the sera of patients with scleroderma, systemic lupus erythematosus, and rheumatoid arthritis. The above antibodies were obtained in preparative amounts. Proceeding from the concept of the idiotypic network, the antibodies were suggested to be natural enzymes and their properties were studied. They appeared to be anti-DNA antibodies, competing with the native topoisomerase I for binding to anti-topoisomerase monoclonal antibodies and possessing highly specific DNA-binding activity (Kd is about 0.1 nM). The antiidiotypic antibodies specifically inhibit the topoisomerase-catalysed relaxation reaction and affect the formation of covalent DNA-protein complex. Possible involvement of antiidiotypic antibodies against topoisomerase in the catalysis of reactions of DNA transformation is analysed. Catalytic antibodies that are natural enzymes possessing DNA-nicking activity have been isolated from the blood sera of patients with different autoimmune pathologies.

摘要

本文讨论了自身免疫血清中天然催化抗体的主要存在情况。在自身免疫过程中,已在硬皮病、系统性红斑狼疮和类风湿性关节炎患者的血清中发现针对拓扑异构酶I的抗独特型抗体。上述抗体已大量制备。根据独特型网络的概念,这些抗体被认为是天然酶,并对其性质进行了研究。它们似乎是抗DNA抗体,与天然拓扑异构酶I竞争结合抗拓扑异构酶单克隆抗体,并具有高度特异性的DNA结合活性(解离常数约为0.1 nM)。抗独特型抗体特异性抑制拓扑异构酶催化的松弛反应,并影响共价DNA-蛋白质复合物的形成。分析了针对拓扑异构酶的抗独特型抗体可能参与DNA转化反应催化的情况。已从患有不同自身免疫性疾病的患者血清中分离出具有DNA切割活性的天然酶催化抗体。

相似文献

10
Anti-topoisomerase I autoantibodies in systemic sclerosis.系统性硬化症中的抗拓扑异构酶I自身抗体
Autoimmun Rev. 2009 Jul;8(8):692-6. doi: 10.1016/j.autrev.2009.02.018. Epub 2009 Feb 13.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验