酶
细胞
肾
细胞内
氨肽酶
血管生成
细胞膜
细胞生物学
化学
生物化学
荧光
生物
生物物理学
病理
癌症研究
医学
氨基酸
亮氨酸
内分泌学
物理
量子力学
作者
Yun Jae Yang,Mingchong Dai,Kyo Han Ahn
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2023-07-05
卷期号:8 (7): 2791-2798
被引量:15
标识
DOI:10.1021/acssensors.3c00730
摘要
Aminopeptidase N (APN), a transmembrane ectoenzyme, plays multifunctional roles in cell survival and migration, angiogenesis, blood pressure regulation, and viral uptake. Abnormally high levels of the enzyme can be found in some tumors and injured liver and kidney. Therefore, noninvasive detection methods for APN are in demand for diagnosing and studying the associated diseases, leading to two dozen activatable small-molecule probes reported up to date. All of the known probes, however, analyze the enzyme activity by monitoring fluorescent molecules inside cells, despite the enzymatic reaction taking place on the outer cell membrane. In this case, different cell permeability and enzyme kinetics can cause false signal data. To address this critical issue, we have developed two cell-membrane-localizing APN probes whose enzymatic products also localize the outer cell membrane. The probes selectively respond to APN with ratiometric fluorescence signal changes. A selected probe, which has two-photon imaging capability, allowed us to determine the relative APN levels in various organ tissues for the first time: 4.3 (intestine), 2.1 (kidney), 2.7 (liver), 3.2 (lung), and 1.0 (stomach). Also, a higher APN level was observed from a HepG2-xenograft mouse tissue in comparison with the normal tissue. Furthermore, we observed a significant APN level increase in the mouse liver of a drug (acetaminophen)-induced liver injury model. The probe thus offers a reliable means for studying APN-associated biology including drug-induced hepatotoxicity simply by ratiometric imaging.
科研通智能强力驱动
Strongly Powered by AbleSci AI