草虾(Palaemonetes pugio)卵磷脂的纯化、单克隆抗体的生成及甲壳类动物脂质卵磷脂检测的验证

Eva Oberdörster, Charles D Rice, Lisa K Irwin
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引用次数: 40

摘要

为了研究潜在的雌激素或抗雌激素内分泌干扰物,人们已经投入了大量的精力来开发针对多种水生脊椎动物的卵黄蛋白原抗体。关于水生无脊椎动物内分泌紊乱的研究很少。虽然已经产生了一些针对蓝蟹和对虾脂卵磷脂的抗体,但它们与重要的河口草虾Palaemonetes pugio的交叉反应性很差。从卵中纯化卵黄蛋白,用标准技术制备单克隆抗体,用ELISA法筛选杂交瘤上清。用雄性和雌性草虾提取物进行Western blots检测单克隆抗体的特异性。发现了68 ~ 85 kD范围内的两条低分子质量带和190 ~ 221 kD范围内的两条高分子质量带。除草虾外,还筛选到蓝蟹(Callinectes sapidus)、泥蟹(Rhithropanopeus harrisii)、克氏原螯虾(Procambarus clarkii)、大水蚤(Daphnia magna)等几种甲壳类动物。为了进一步调查抗体的使用情况,我们进行了一项为期6周的慢性芘暴露研究。我们发现6周后卵磷脂在雌性中上调,这可能是对亲脂性外源性药物的保护措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Purification of vitellin from grass shrimp Palaemonetes pugio, generation of monoclonal antibodies, and validation for the detection of lipovitellin in Crustacea

Much effort has been put into developing vitellogenin antibodies against a wide variety of aquatic vertebrate species to study potential estrogen or anti-estrogen endocrine disrupters. Little work has been done on endocrine disruption in aquatic invertebrates. Although some antibodies have been produced against blue crab and penaeid shrimp lipovitellin, they have only poor cross-reactivity with the important estuarine grass shrimp, Palaemonetes pugio. Vitellin was purified from eggs, monoclonal antibodies were produced using standard techniques, and hybridoma supernatants were screened by ELISA. Western blots were done using extracts from male and female grass shrimp to verify specificity of the monoclonal antibodies. Two low molecular mass bands in the range of 68–85 kD and two high molecular mass bands in the range of 190–221 kD were found. In addition to grass shrimp, several other crustacean species were screened and cross-reactivity found, including blue crab (Callinectes sapidus), mud crab (Rhithropanopeus harrisii), red swamp crayfish (Procambarus clarkii) and Daphnia magna. To further investigate the use of the antibody, we performed a chronic 6-week pyrene exposure study. We found that vitellin was upregulated in females after 6 weeks and that this may be a protective measure against lipophilic xenobiotics.

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