Guzaeva T V, Komarov A M, Yurov S V, Chudinov A V, Afanasiev S S
Institute of Immunology, State Concern Biopreparation, Lyubuchany, Moscow Region, Russian Federation.
Immunol Lett. 1993 Mar;35(3):285-9. doi: 10.1016/0165-2478(93)90196-9.
The conditions of protein A labelling with Eu chelates were studied. The conjugates obtained were compared with those from horseradish peroxidase used conventionally in immunochemical practice. Protein A-Eu conjugates were obtained by a method applied previously for antibody labelling with indium and europium chelates using the bicyclic dianhydride of diethylenetriaminepenta-acetic acid (DADTPA) with some modifications. The Eu-labeled protein A ensured a sensitivity of the IgG determination at the level of 2 ng/ml and a dynamic range of the determination from 3 to 1000 ng/ml, which significantly exceed analogous values for the protein A-peroxidase conjugates. The Eu-labeled protein A was used for the determination of antibodies to Francisella tularensis in the sera of humans vaccinated against tularemia. The assay values exceeded by 10-40-fold the results of an ELISA in sensitivity. It was deduced that the Eu-labeled protein A can be effectively used for the determination of antibodies specific to a tularemia causative agent. In particular, this compound can be useful for the determination of specific antibodies in low immune sera.
研究了用铕螯合物标记蛋白A的条件。将得到的缀合物与免疫化学实践中常规使用的辣根过氧化物酶缀合物进行比较。蛋白A-铕缀合物是通过先前用于用铟和铕螯合物标记抗体的方法获得的,该方法使用二乙烯三胺五乙酸双环二酐(DADTPA)并做了一些修改。铕标记的蛋白A确保IgG测定的灵敏度为2 ng/ml,测定的动态范围为3至1000 ng/ml,这显著超过了蛋白A-过氧化物酶缀合物的类似值。铕标记的蛋白A用于测定接种兔热病疫苗的人血清中针对土拉弗朗西斯菌的抗体。该检测值在灵敏度上比ELISA结果高出10至40倍。推断铕标记的蛋白A可有效用于测定土拉菌病病原体特异性抗体。特别是,该化合物可用于测定低免疫血清中的特异性抗体。