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In vitro synthesis of a type A trichothecenes complete antigen from T-2 toxin

机译:从T-2毒素体外合成A型毛滴虫毒素完全抗原

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We report the artificial synthesis from T-2 toxin of a type A trichothecenes complete antigen. First, 3-Ac-T-2 was made from T-2 following acetylation. Then 3-Ac-NEOS as a T-2 skeleton structure was synthesized by enzymolysis and identified by liquid chromatography-tandem mass spectrometry and nuclear magnetic resonance. Next, a hapten (3-Ac-NEOS-HS) was formed by modifying the C8 position of 3-Ac-NEOS using succinic anhydride method. 3-Ac-NEOS-HS-BSA/-OVA were prepared by conjugating hapten with bovine serum albumin (BSA) or ovalbumin (OVA) by carbodiimide method and identified by UV spectroscopy and sodium dodecyl sulphate-polyacrylamide gel electrophoresis. Results showed that conjugation ratio of 3-Ac-NEOS-HS to BSA was 8.76: 1 and OVA 7.24: 1, indicating 3-Ac-NEOS-HS-BSA as a complete antigen was better. Next we used it to immunize rabbits and obtained a 1:64,000 antibody titre. In conclusion, a type A trichothecenes complete antigen was successfully synthesized, which was the foundation for antibody preparation and enzyme-linked immunosorbent assay kit development for all type A trichothecenes (parent?+?modified/masked type A trichothecenes).
机译:我们报告从人工合成的T-2毒素的A型毛滴虫病完全抗原。首先,乙酰化后由T-2制成3-Ac-T-2。然后通过酶解合成3-Ac-NEOS作为T-2骨架结构,并通过液相色谱-串联质谱和核磁共振法进行鉴定。接下来,通过使用琥珀酸酐法修饰3-Ac-NEOS的C8位置来形成半抗原(3-Ac-NEOS-HS)。通过碳二亚胺法将半抗原与牛血清白蛋白(BSA)或卵清蛋白(OVA)缀合制备3-Ac-NEOS-HS-BSA / -OVA,并通过紫外光谱和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳进行鉴定。结果表明3-Ac-NEOS-HS-BSA的结合率为8.76:1,OVA为7.24:1,表明3-Ac-NEOS-HS-BSA作为完全抗原的结合率更好。接下来,我们将其用于免疫兔,并获得1:64,000的抗体效价。总之,成功地合成了A型毛滴虫的完全抗原,这为所有A型毛滴虫(亲本+ +修饰的/掩蔽的A型毛滴虫)的抗体制备和酶联免疫吸附试剂盒的开发奠定了基础。

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