体内
荧光
荧光团
化学
连接器
荧光寿命成像显微镜
生物物理学
酶
临床前影像学
生物标志物
生物化学
癌症研究
生物
生物技术
物理
操作系统
量子力学
计算机科学
作者
Zhiliang Luo,Liandong Feng,Ruibing An,Guanfu Duan,Runqi Yan,Hua Shi,Jian He,Zhengyang Zhou,Changge Ji,Hong‐Yuan Chen,Deju Ye
标识
DOI:10.1002/chem.201702210
摘要
Abstract γ‐Glutamyl transpeptidase (GGT) is a cell‐membrane‐bound enzyme that is involved in various physiological and pathological processes and is regarded as a potential biomarker for many malignant tumors, precise detection of which is useful for early cancer diagnosis. Herein, a new GGT‐activatable near‐infrared (NIR) fluorescence imaging probe (GANP) by linking of a GGT‐recognitive substrate γ‐glutamate (γ‐Glu) and a NIR merocyanine fluorophore (mCy‐Cl) with a self‐immolative linker p ‐aminobenzyl alcohol (PABA) is reported. GANP was stable under physiological conditions, but could be efficiently activated by GGT to generate ≈100‐fold enhanced fluorescence, enabling high sensitivity (detection limit of ≈3.6 mU L −1 ) and specificity for the real‐time imaging of GGT activity as well as rapid evaluation of the inhibition efficacy of GGT inhibitors in living tumor cells. Notably, the deep tissue penetration ability of NIR fluorescence could further allow GANP to image GGT in frozen tumor tissue slices with large penetration depth (>100 μm) and in xenograft tumors in living mice. This GGT activatable NIR fluorescence imaging probe could facilitate the study and diagnosis of other GGT‐correlated diseases in vivo.
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