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Electrochemical detection of endotoxin using recombinant factor C zymogen

机译:重组C因子酶原电化学检测内毒素

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We have developed a zymogen-based electrochemical sensor. Zymogen is an inactive enzyme precursor (proenzyme) and it is necessary to transform it biochemically (e.g., by hydrolysis and conformational change) to make it an active enzyme. In this study, we demonstrated the detection of endotoxin by using recombinant Factor C (rFC), which is a protease zymogen activated by endotoxin binding. The activated rFC hydrolyzes a synthetic substrate of Boc-Val-Pro-Arg-p-nitroanilnide to generate an electrochemical active compound, p-nitroaniline (pNA). The liberated pNA was detected by differential pulse voltammetry at -0.75 V. By using this electrochemical process, 5000 endotoxin units (EU) L~(-1) and 1000 EU L~(-1) were detected in a Tris-Ac buffer with a pH of 7.5 at 37 °C for reaction times of 1 h and 3 h, respectively. The concept of zymogen-based electrochemical sensors is expected to lead to the development of new biosensors.
机译:我们开发了一种基于酶原的电化学传感器。酶原是一种无活性的酶前体(原酶),有必要对其进行生化转化(例如,通过水解和构象变化)以使其成为活性酶。在这项研究中,我们证明了通过使用重组因子C(rFC)来检测内毒素,重组因子C是被内毒素结合激活的蛋白酶酶原。活化的rFC水解Boc-Val-Pro-Arg-对硝基苯胺的合成底物,生成电化学活性化合物对硝基苯胺(pNA)。在-0.75 V下通过差示脉冲伏安法检测到释放的pNA。通过这种电化学过程,在Tris-Ac缓冲液中,检测到5000内毒素单位(EU)L〜(-1)和1000 EU L〜(-1)。在37°C下pH值为7.5,反应时间分别为1 h和3 h。基于酶原的电化学传感器的概念有望导致新的生物传感器的发展。

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