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使用N-(氨基苯甲酰氧基)琥珀酰亚胺作为双功能异源双功能试剂来制备半抗原-蛋白质缀合物。柔红霉素作为具有氨基的模型半抗原。

The use of N-(aminobenzoyloxy) succinimide as a two-level heterobifunctional agent for the preparation of hapten-protein conjugates. Daunomycin as a model hapten with an amino group.

作者信息

Fujiwara K, Matsumoto N, Kitagawa T, Inouye K

机构信息

Faculty of Pharmaceutical Sciences, Nagasaki University, Japan.

出版信息

J Immunol Methods. 1990 Dec 5;134(2):227-35. doi: 10.1016/0022-1759(90)90384-8.

Abstract

Three geometric ortho-, meta-, and para-isomers of N-(aminobenzoyloxy)succinimide (ABS) were synthesized, and their usefulness as a two-level heterobifunctional cross-linking agent in the preparation of hapten-protein conjugates was evaluated. The conjugation was based on the principle that ABS reacts immediately with an amino group of a hapten, and an aminobenzoyl group incorporated into the hapten is then activated by diazotization to a functional diazobenzoyl group acting on tyrosine or histidine residues of the protein. Using the anti-tumor antibiotic daunomycin (DM) as a model hapten, the three isomers of ABS were compared for their ability to conjugate DM with bovine serum albumin (BSA); DM incorporation onto a BSA molecular was found to occur to the highest degree with m-ABS, followed by p-ABS. while o-ABS completely failed to conjugate under the same coupling conditions. Using m-ABS it was possible to introduce more than 10 molecules of DM per BSA molecule. One of the DM-BSA samples was used as the immunogen for the production of anti-DM serum in a rabbit. The antibody specificity was shown to be direct to DM but not to other anti-cancer drugs (bleomycin, mitomycin C, actinomycin D and 5-fluorouracil) by the double antibody enzyme immunoassay (DEIA) using DM-beta-galactosidase conjugate as a label. An enzyme-linked immunosorbent assay (ELISA) for anti-DM IgG was developed using a DM-human serum albumin (DM-HSA) conjugate similarly prepared with m-ABS and horseradish peroxidase-conjugated goat anti-rabbit IgG as the solid-phase antigen and the labelled second antibody, respectively. This ELISA permitted us to measure accurately as little as 50 ng of anti-DM IgG per ml using a standard anti-DM IgG which had been purified from the anti-DM serum using an affinity column of Sepharose 4B with DM-HSA as the ligand. Using this ELISA as well as a sandwich enzyme immunoassay (SEIA) for total IgG, serum levels of anti-DM IgG and total IgG levels were easily monitored in a rabbit following immunization with DM-BSA. These results indicate that the use of DBS provides a novel method for preparing hapten-protein conjugates which will be useful in biochemistry and immunochemistry.

摘要

合成了N-(氨基苯甲酰氧基)琥珀酰亚胺(ABS)的三种几何邻位、间位和对位异构体,并评估了它们作为二级异双功能交联剂在制备半抗原-蛋白质缀合物中的效用。缀合基于以下原理:ABS立即与半抗原的氨基反应,然后通过重氮化将引入半抗原中的氨基苯甲酰基活化成作用于蛋白质酪氨酸或组氨酸残基的功能性重氮苯甲酰基。以抗肿瘤抗生素柔红霉素(DM)作为模型半抗原,比较了ABS的三种异构体将DM与牛血清白蛋白(BSA)缀合的能力;发现间位ABS使DM掺入BSA分子的程度最高,其次是对位ABS。而邻位ABS在相同的偶联条件下完全无法缀合。使用间位ABS,每个BSA分子可以引入超过10个DM分子。其中一个DM-BSA样品用作免疫原,在兔体内产生抗DM血清。通过使用DM-β-半乳糖苷酶缀合物作为标记的双抗体酶免疫测定(DEIA),显示抗体特异性直接针对DM,而不针对其他抗癌药物(博来霉素、丝裂霉素C、放线菌素D和5-氟尿嘧啶)。使用类似地用间位ABS制备的DM-人血清白蛋白(DM-HSA)缀合物作为固相抗原,辣根过氧化物酶缀合的山羊抗兔IgG作为标记的二抗,开发了一种用于抗DM IgG的酶联免疫吸附测定(ELISA)。这种ELISA使我们能够使用从抗DM血清中使用以DM-HSA作为配体的琼脂糖4B亲和柱纯化的标准抗DM IgG,准确测量低至每毫升50 ng的抗DM IgG。使用这种ELISA以及用于总IgG的夹心酶免疫测定(SEIA),在用DM-BSA免疫后的兔中可以轻松监测抗DM IgG的血清水平和总IgG水平。这些结果表明,使用DBS提供了一种制备半抗原-蛋白质缀合物的新方法,这在生物化学和免疫化学中将是有用的。

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