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Detection and Quantification of Ricin in Beverages Using Isotope Dilution Tandem Mass Spectrometry

机译:同位素稀释串联质谱法检测和定量分析饮料中蓖麻毒素

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摘要

The toxic plant protein ricin has gained notoriety due to wide availability and potential use as a bioterrorism agent, with particular concern for food supply contamination. We have developed a sensitive and selective mass spectrometry-based method to detect ricin in tap water, 2percent milk, apple juice, and orange juice. Ricin added to beverage matrices was extracted using antibody-bound magnetic beads and digested with trypsin. Absolute quantification was performed using isotope dilution mass spectrometry with a linear ion trap operating in product-ion-monitoring mode. The method allows for identification of ricin A chain and B chain and for distinction of ricin from ricin agglutinin within a single analytical run. Ricin-bound beads were also tested for deadenylase activity by incubation with a synthetic ssDNA oligomer. Depurination of the substrate by ricin was confirmed by matrix-assisted laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOFMS). This method was used successfully to extract ricin from each beverage matrix. The activity of recovered ricin was assessed, and quantification was achieved, with a limit of detection of 10 fmol/mL (0.64 ng/mL).
机译:有毒的植物蛋白蓖麻毒蛋白因其广泛的可获得性和作为生物恐怖剂的潜在用途而臭名昭著,尤其是对食品供应的污染。我们已经开发了一种基于灵敏和选择性质谱的方法来检测自来水,2%牛奶,苹果汁和橙汁中的蓖麻毒蛋白。使用结合抗体的磁珠提取添加到饮料基质中的蓖麻毒素,并用胰蛋白酶消化。使用同位素稀释质谱法以在产物离子监测模式下运行的线性离子阱进行绝对定量。该方法可在一次分析过程中鉴定蓖麻毒蛋白A链和B链,并区分蓖麻毒蛋白与蓖麻毒蛋白凝集素。还通过与合成的ssDNA寡聚物孵育,测试了与蓖麻毒素结合的珠的去甲腺苷酸酶活性。基质辅助激光解吸电离飞行时间质谱(MALDI-TOFMS)证实了蓖麻毒素对底物的提纯。该方法已成功用于从每种饮料基质中提取蓖麻毒蛋白。评估回收的蓖麻毒蛋白的活性,并达到定量,检测极限为10 fmol / mL(0.64 ng / mL)。

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