首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Characterization of 9H-(1,3-dichlor-9,9-dimethylacridin-2-ona-7-yl)-phosphate (DDAO) as substrate of PP-2A in a fluorimetric microplate assay for diarrhetic shellfish toxins (DSP)
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Characterization of 9H-(1,3-dichlor-9,9-dimethylacridin-2-ona-7-yl)-phosphate (DDAO) as substrate of PP-2A in a fluorimetric microplate assay for diarrhetic shellfish toxins (DSP)

机译:用于腹泻性贝类毒素(DSP)的荧光微板测定法表征9H-(1,3-二氯-9,9-二甲基ac啶-2--2-7-7-基)磷酸酯(DDAO)作为PP-2A的底物

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摘要

Specific inhibition of protein-phosphatases by diarrhetic shellfish toxins (DSP) of the okadaic acid group, has led to the development of a fluorescent enzyme inhibition assay for these toxins using protein-phosphatase 2A (PP-2A) and fluorogenic substrates of the enzyme. Two different substrates of PP-2A have been previously used in this microplate assay: 4-methylumbelliferyl phosphate and fluorescein diphosphate (FDP). In this report, we present the results obtained using a new fluorogenic substrate of PP-2A, the compound dimethylacridinone phosphate (DDAO). A linear relationship between PP-2A concentration and DDAO-induced fluorescence was observed, Okadaic acid (0.0157-9.43 nhl)-dependent inhibition of phosphatase activity showed similar results using FDP and DDAO. Recovery percentages obtained with FDP and DDAO in spiked mussel samples (both raw and canned) were very similar and reproducible. Comparative analysis of DSP-contaminated mussel samples by HPLC and FDP/DDAO-PP-2A showed a good correlation among all methods, thus demonstrating that DDAO can be used as a fluorogenic substrate to quantify okadaic acid and related toxins in bivalve molluscs with optimum reliability. (C) 2000 Elsevier Science Ltd. All rights reserved. [References: 10]
机译:冈田酸类的腹泻性贝类毒素(DSP)对蛋白磷酸酶的特异性抑制,导致开发了使用蛋白磷酸酶2A(PP-2A)和该酶的荧光底物对这些毒素进行荧光酶抑制测定的方法。在该微孔板测定中先前已使用了两种不同的PP-2A底物:4-甲基伞形磷酸酯和二磷酸荧光素(FDP)。在本报告中,我们介绍了使用新的PP-2A荧光底物即化合物二甲基ac啶酮磷酸酯(DDAO)获得的结果。观察到PP-2A浓度与DDAO诱导的荧光之间存在线性关系,冈田酸(0.0157-9.43 nhl)依赖性的磷酸酶活性抑制作用使用FDP和DDAO表现出相似的结果。用FDP和DDAO获得的加标贻贝样品(原始和罐装)的回收率非常相似且可重复。通过HPLC和FDP / DDAO-PP-2A对被DSP污染的贻贝样品进行的比较分析表明,所有方法之间都具有良好的相关性,从而证明DDAO可以用作荧光底物,定量分析双壳贝类中的冈田酸和相关毒素,具有最佳的可靠性。 (C)2000 Elsevier ScienceLtd。保留所有权利。 [参考:10]

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