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Development of interdigitated electrode based enzyme sensor for triglyceride monitoring using engineered oxygen insensitive glycerol 3-phosphate oxidase

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SENSORS AND ACTUATORS REPORTS
卷 5, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.snr.2023.100164

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Triglycerides; Glycerol 3 -phosphate oxidase; Oxidative half reaction; Dehydrogenase; Enzyme sensor; Disposable sensor; Interdigitated electrode

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In this study, researchers constructed a TG sensor using engineered glycerol 3-phosphate oxidase (GlpO) and electrochemical detection. By using disposable interdigitated electrode (IDE), a highly sensitive electrochemical sensor for TG was achieved, with a sensitivity of 0.4 μA/mM, 2.4 times higher than that of the conventional screen-printed carbon electrode (SPCE).
Triglycerides (TG) are an important biomarker of various diseases including hyper-lipidemia. Current emergent requirements for TG sensing include the development of electrochemical sensors for easy, cost-effective, disposable and single use triglyceride sensors. We propose a TG sensor using an engineered glycerol 3-phosphate oxidase (GlpO) and electrochemical detection. In this study, we aimed to develop an electrochemical TG sensor based on engineering the oxidative half reaction of GlpO to be oxygen insensitive, with the employment of an interdigitated electrode (IDE). To construct an oxygen insensitive mutant GlpO, we constructed a double mutant, Met104Phe/Asp169Glu, which revealed an engineered GlpO exhibiting repressed oxidase activity, while its dyemediated dehydrogenase activity enhanced. The electrochemical enzyme sensor was constructed for the measurement of TG based on engineered GlpO using disposable screen-printed carbon electrode (SPCE) or disposable IDE using Ru complex as the electron mediator. By using the disposable IDE sensor, a highly sensitive electrochemical sensor for Glp was achieved, with the sensitivity of 0.4 & mu;A/mM. The improved sensitivity was 2.4 times higher than that of SPCE (0.17 & mu;A/mM), with LOD of 0.022 mM. Furthermore, the dry sensor strip, where the double mutant GlpO and Ru complex were dropcasted and dried on the IDE, was prepared and the Glp concentration was successfully measured in the delipidized serum solution. Therefore, by the employment of the established pretreatment method for TG to release Glp, a highly sensitive, accurate, easy and rapid electrochemical measurement method for TG will be developed using constructed M104F/D169E mutant GlpO with the combination of IDE.

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