化学
碱性磷酸酶
模块化设计
胺气处理
萘
鉴定(生物学)
色谱法
生物化学
有机化学
酶
程序设计语言
植物
计算机科学
生物
作者
Yifan Ma,Kai Wang,Hui‐Jing Li,Xilin Wang,Rongmei Kong,Yan Zhao,Weiheng Kong,Fengli Qu
标识
DOI:10.1021/acs.analchem.5c05007
摘要
Accurate detection of alkaline phosphatase (ALP) is critical for clinical diagnosis and mechanistic studies across diverse tissues. Here, we present a modular "off-on" fluorescent probe platform based on 1-naphthol phosphate sodium (1-NPP) and ethylenediamine (EDA), enabling precise, rapid, and cost-effective quantification of ALP activity from serum to whole organs. The probe's mechanism relies on the ALP-catalyzed hydrolysis of 1-NPP to liberate 1-naphthol, which subsequently reacts with EDA to generate a robust fluorescent signal. This system demonstrates high sensitivity, with a detection limit of 0.068 mU/mL, and maintains excellent linearity and stability across complex biological matrices including serum, cell lysates, and tissue homogenates. Application in various cell lines and mice organs revealed organ- and disease-specific ALP activity distributions, highlighting its utility for distinguishing physiological and pathological states. The probe's low cytotoxicity and straightforward preparation offer significant advantages over nanoparticle-based sensors. Overall, this work establishes a versatile and scalable platform for ALP analysis, whose remarkable ability to distinguish ALP activity across cells and organs underpins its broad potential for early disease surveillance, mechanistic exploration, and high-throughput screening.
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