[l -赖氨酸α -氧化酶与抗体结合物的合成]。

Voprosy meditsinskoi khimii Pub Date : 2000-07-01
N V Gogichaeva, E V Lukasheva, E M Gavrilova, I P Smirnova, A M Egorov, T T Berezov
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引用次数: 0

摘要

药物与载体分子的偶联能够获得治疗制剂,该制剂可被运输到选定的靶器官。本文阐述了抗肿瘤酶l -赖氨酸-氧化酶与抗体结合的方法。通过在抗体表面上与l -赖氨酸α -氧化酶分子(初始酶活性的0.2%)中产生的醛基团或与交联分子的醛基团结合形成偶联物。以含乙醛基团的氧化过氧化物酶为交联剂时,l -赖氨酸α -氧化酶活性最高(78%)。戊二醛法的酶活性为初始酶活性的70%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Synthesis of conjugates of L-lysine alpha-oxidase with antibodies].

The conjugation of the drugs with vector molecules enables to obtain therapeutic preparation, which may be transported to the selected target organ. In the present work the methods of conjugation of antineoplastic enzyme L-lysine alpha-oxidase with antibodies were elaborated. Conjugates were worked out through the attachment of amino groups on the antibody surface either with the aldehyde groups which were created in L-lysine alpha-oxidase molecule (0.2% of initial enzymatic activity) or with the aldehyde groups of cross-linking molecules. Maximal (78%) L-lysine alpha-oxidase activity in conjugates was observed when oxidized peroxidase which contained the aldehyde groups was used as crosslinking agent. The glutaraldehyde method yielded 70% of initial enzyme activity.

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