化学
无机焦磷酸酶
己糖激酶
焦磷酸酶
焦磷酸盐
检出限
色谱法
线性范围
三磷酸腺苷
基质(水族馆)
二磷酸腺苷
生物化学
酶
糖酵解
海洋学
血小板
血小板聚集
免疫学
生物
地质学
作者
Junhyun Park,Hyogu Han,Chihyun Park,Jun Ki Ahn
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2022-08-15
卷期号:94 (33): 11508-11513
被引量:11
标识
DOI:10.1021/acs.analchem.2c01412
摘要
In this study, we demonstrated a personal glucose meter-based method for washing-free and label-free inorganic pyrophosphatase (PPase) detection, which relies on the cascade enzymatic reaction (CER) promoted by hexokinase and pyruvate kinase. In principle, the absence of target PPase enables adenosine triphosphate sulfurylase to catalyze the conversion of pyrophosphate (PPi) to ATP, a substrate of CER, which results in the significant reduction of glucose levels by the effective CER process. In contrast, the PPi cleavage activity works in the presence of target PPase by decomposing PPi to orthophosphate (Pi). Therefore, the CER process cannot be effectively executed, leading to the maintenance of the initial high glucose level that may be measured by a portable personal glucose meter. Based on this novel strategy, a quantitative evaluation of the PPase activity may be achieved in a dynamic linear range of 1.5–25 mU/mL with a detection limit of 1.18 mU/mL. Compared with the previous PPase detection methods, this method eliminates the demand for expensive and bulky analysis equipment as well as a complex washing step. More importantly, the diagnostic capability of this method was also successfully verified by reliably detecting PPase present in an undiluted human serum sample with an excellent recovery ratio of 100 ± 2%.
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