首页> 外国专利> QUANTITATIVE METHOD FOR DETECTING YESSOTOXINS IN FISHERY PRODUCTS BASED ON THE ACTIVATION CAUSED BY THE TOXIN IN CELLULAR PHOSPHODIESTERASE

QUANTITATIVE METHOD FOR DETECTING YESSOTOXINS IN FISHERY PRODUCTS BASED ON THE ACTIVATION CAUSED BY THE TOXIN IN CELLULAR PHOSPHODIESTERASE

机译:基于纤维素磷酸酯酶中毒素引起的活化的水产品中毒素定量的定量方法

摘要

The present invention relates to a quantitative method for detecting yessotoxins in fishery products based on the activation the toxin produces on cellular phosphodiesterases and the therapeutic use of this activation. The cellular target of yessotoxin (YTX) and its analogs is the activation of phosphodiesterases (PDEs). The PDEs-YTX bond produces a measurable signal. The bond can be quantified by means of an affinity biosensor or by fluorescence. The biosensor detects biomolecular interactions and allows determining the presence of YTX due to its interaction with PDEs. The variations in the degradation rate of the fluorescent derivative anthraniloyl-cAMP are determined by means of plate fluorescence. The rate at which the PDEs degrade this molecule increases in the presence of YTX. YTX inhibits immunological activation of mastocytes in rats and induces a cytotoxic effect in human hepatocarcinoma cells, which implies two therapeutic uses of YTXs as an antiallergic and antitumor compound.
机译:本发明涉及基于毒素在细胞磷酸二酯酶上产生的活化作用和该活化作用的治疗用途,用于检测渔业产品中异毒素的定量方法。 Yessotoxin(YTX)及其类似物的细胞靶标是磷酸二酯酶(PDE)的激活。 PDEs-YTX键产生可测量的信号。可以通过亲和生物传感器或通过荧光定量键。生物传感器检测生物分子相互作用,并由于其与PDE的相互作用而允许确定YTX的存在。荧光衍生物蒽基-cAMP的降解速率的变化通过平板荧光来确定。在存在YTX的情况下,PDE降解该分子的速率增加。 YTX抑制大鼠肥大细胞的免疫学激活并诱导人肝癌细胞的细胞毒性作用,这意味着YTX作为抗过敏和抗肿瘤化合物的两种治疗用途。

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