首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Detection of residual toxin in tissues of ricin-poisoned mice by sandwich enzyme-linked immunosorbent assay and immunoprecipitation
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Detection of residual toxin in tissues of ricin-poisoned mice by sandwich enzyme-linked immunosorbent assay and immunoprecipitation

机译:夹心酶联免疫吸附法和免疫沉淀法检测蓖麻毒素中毒小鼠组织中的残留毒素

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摘要

This work aimed to evaluate a method to detect the residual ricin in animal tissues. Immunoprecipitation and sandwich enzyme-linked immunosorbent assay (ELISA) were used to detect ricin in the tissues of intoxicated mice. The monoclonal antibodies (Mabs) 4C13 and 3D74 were used to assay the whole ricin molecules via sandwich ELISA. Mab 4C13 was conjugated with Sepharose 4B to capture ricin or ricin A chain by immunoprecipitation. Mice injected intravenously with ricin at the dosage of 5 μg/mouse were killed at different time points after intoxication. The serum, liver, kidney, lung, and intestine were harvested. High levels of ricin were found in serum and liver samples at each poisoning time point by sandwich ELISA, suggesting the possibility of determining ricin intoxication by detecting residual ricin in the serum. However, this method turned out to be ineffective for examining ricin in the kidney, lung, and intestine of poisoned mice. Although the same tissue samples of intoxicated mice were analyzed by immunoprecipitation, positive bands were found. This indicated that some components in the kidney, lung, and intestine could bind with ricin and interfere in its binding activity with the coated antibody. Immunoprecipitation could be used to measure the existence of ricin in these samples.
机译:这项工作旨在评估一种检测动物组织中残留蓖麻毒素的方法。免疫沉淀和三明治酶联免疫吸附试验(ELISA)用于检测中毒小鼠组织中的蓖麻毒蛋白。单克隆抗体(Mabs)4C13和3D74用于通过夹心ELISA分析整个蓖麻毒蛋白分子。将单克隆抗体4C13与琼脂糖凝胶4B偶联,通过免疫沉淀捕获蓖麻毒蛋白或蓖麻毒蛋白A链。在中毒后的不同时间点处以5μg/小鼠的剂量静脉注射蓖麻毒蛋白杀死小鼠。收集血清,肝,肾,肺和肠。通过夹心ELISA在每个中毒时间点在血清和肝脏样品中发现高水平的蓖麻毒蛋白,提示通过检测血清中残留的蓖麻毒蛋白来确定蓖麻毒蛋白中毒的可能性。但是,该方法对检查中毒小鼠的肾脏,肺和肠中的蓖麻毒蛋白无效。尽管通过免疫沉淀法分析了醉酒小鼠的相同组织样品,但发现了阳性条带。这表明肾,肺和肠中的某些成分可能与蓖麻毒蛋白结合并干扰其与被包被抗体的结合活性。免疫沉淀可用于测量这些样品中蓖麻毒素的存在。

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