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Fluorometric Method for Inorganic Pyrophosphatase Activity Detection and Inhibitor Screening Based on Click Chemistry

机译:基于点击化学的无机焦磷酸酶活性的荧光测定和抑制剂筛选

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摘要

A fluorometric method for pyrophosphatase (PPase) activity detection was developed based on click chemistry. Cu(II) can coordinate with pyrophosphate (PPi), the addition of pyrophosphatase (PPase) into the above system can destroy the coordinate compound because PPase catalyzes the hydrolysis of PPi into inorganic phosphate and produces free Cu(II), and free Cu(II) can be reduced by sodium ascorbate (SA) to form Cu(I), which in turn initiates the ligating reaction between nonfluorescent 3-azidocoumarins and terminal alkynes to produce a highly fluorescent triazole complex, based on which, a simple and sensitive turn on fluorometric method for PPase can be developed. The fluorescence intensity of the system has a linear relationship with the logarithm of the PPase concentration in the range of 0.5 and 10 mU with a detection limit down to 0.2 mU (S/N = 3). This method is cost-effective and convenient without any labels or complicated operations. The proposed system was applied to screen the potential PPase inhibitor with high efficiency. The proposed method can be applied to diagnosis of PPase-related diseases.
机译:基于点击化学,开发了一种荧光检测焦磷酸酶(PPase)活性的方法。 Cu(II)可以与焦磷酸盐(PPi)配位,在上述系统中添加焦磷酸酶(PPase)可以破坏配位化合物,因为PPase催化PPi水解为无机磷酸盐并生成游离的Cu(II)和游离的Cu( II)可以被抗坏血酸钠(SA)还原形成Cu(I),而Cu(I)则引发无荧光的3-azidocoumarins与末端炔烃之间的连接反应,产生高荧光的三唑配合物,在此基础上,简单而灵敏的转变可以开发用于PPase的荧光法。系统的荧光强度与PPase浓度的对数在0.5和10 mU之间呈线性关系,检出限低至0.2 mU(S / N = 3)。此方法经济高效且方便,无需任何标签或复杂的操作。拟议的系统应用于高效筛选潜在的PPase抑制剂。该方法可用于PPase相关疾病的诊断。

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