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携带肌苷酸表位内影像的单克隆抗体的研制及其在鱼粉竞争性酶联免疫吸附测定中的应用

Development of monoclonal antibodies bearing the internal image of the gizzerosine epitope and application in a competitive ELISA for fish meal.

作者信息

Manosalva Headdy, De Ioannes Alfredo E, Becker María Inés

机构信息

Laboratory of Immunology, Department of Research and Development, BIOSONDA Corp., Santiago, Chile.

出版信息

Hybrid Hybridomics. 2004 Feb;23(1):45-54. doi: 10.1089/153685904322772024.

Abstract

Gizzerosine (GZ), a derivative of histamine, is a biogenic amine found in fish meal, and one of the causative agents of black vomit, a poultry disease. We describe here the preparation of anti-idiotype antibodies to the anti-GZ monoclonal antibody (anti-GZ 3H4) and their possible application to an immunoassay. BALB-c mice were immunized with anti-GZ 3H4 antibody coupled to hemocyanin from Concholepas concholepas. Using somatic cell fusion between NSO/2 cells and splenic lymphocytes from the immunized mice, we obtained 34 potential anti-idiotype antibodies. They were characterized by passive agglutination with supernatants from hybridoma cultures and latex particles conjugated to the idiotype. Anti-idiotype antibodies were analyzed by a competitive RIA, to determine their ability to dissociate the interaction between (125)I-GZ and the anti-GZ 3H4-idiotype antibody. They were also characterized by GZ inhibition of latex passive agglutination assay. Three anti-idiotypes named 2D11, 2H6, and 3A12, all of the IgG isotype, were obtained. They were evaluated by a competitive ELISA, in which GZ competes with the tracer (HRP-idiotype). All presented sensitivity in the range of 0.1-10 microg/mL of GZ; and the 3A12 anti-idiotype antibody showed the best performance. An ELISA was developed using the idiotype bound to the solid phase and the anti-idiotype 3A12-HRP as the tracer. The assay showed a similar sensitivity and cross-reactivity with histamine was only observed at concentrations over 10 microg/mL. Lysine and histidine did not interfere with the assay up to 500 microg/mL. An experiment was conducted with fish meal contaminated with synthetic GZ. The results are promising, and showed that no other compounds of the fish meal interfere with the ELISA system; however the extraction procedure of the sample needs to be improved. From the results presented here, we conclude that the idiotype anti-idiotype ELISA would be an appropriate method to determine GZ in fish meal.

摘要

组胺衍生物吉泽罗辛(GZ)是一种存在于鱼粉中的生物胺,也是家禽疾病“黑吐病”的病原体之一。我们在此描述了抗吉泽罗辛单克隆抗体(抗-GZ 3H4)的抗独特型抗体的制备及其在免疫测定中的可能应用。用与海螺血蓝蛋白偶联的抗-GZ 3H4抗体免疫BALB-c小鼠。通过NSO/2细胞与免疫小鼠脾淋巴细胞之间的体细胞融合,我们获得了34种潜在的抗独特型抗体。通过用杂交瘤培养上清液和与独特型偶联的乳胶颗粒进行被动凝集来对它们进行表征。通过竞争性放射免疫分析对抗独特型抗体进行分析,以确定它们解离(125)I-GZ与抗-GZ 3H4独特型抗体之间相互作用的能力。它们还通过GZ抑制乳胶被动凝集试验进行表征。获得了三种抗独特型抗体,分别命名为2D11、2H6和3A12,均为IgG同种型。通过竞争性酶联免疫吸附测定(ELISA)对它们进行评估,其中GZ与示踪剂(辣根过氧化物酶-独特型)竞争。所有抗体对GZ的检测灵敏度范围为0.1-10微克/毫升;3A12抗独特型抗体表现最佳。使用结合到固相上的独特型和抗独特型3A12-辣根过氧化物酶作为示踪剂开发了一种ELISA。该测定显示出相似的灵敏度,并且仅在浓度超过10微克/毫升时才观察到与组胺的交叉反应。赖氨酸和组氨酸在浓度高达500微克/毫升时不干扰该测定。对受合成GZ污染的鱼粉进行了一项实验。结果很有前景,表明鱼粉中的其他化合物不会干扰ELISA系统;然而,样品的提取程序需要改进。根据此处给出的结果,我们得出结论,独特型-抗独特型ELISA将是测定鱼粉中GZ的合适方法。

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