荧光团
碱性磷酸酶
原位
生物物理学
酶
化学
酶分析
荧光
共焦
斯托克斯位移
生物化学
分子探针
光学
生物
物理
有机化学
DNA
作者
Hong‐Wen Liu,Ké Li,Xiaoxiao Hu,Longmin Zhu,Qiming Rong,Yongchao Liu,Xiaobing Zhang,Jens Hasserodt,Fengli Qu,Weihong Tan
标识
DOI:10.1002/anie.201705747
摘要
Current enzyme-responsive, fluorogenic probes fail to provide in situ information because the released fluorophores tend to diffuse away from the reaction sites. The problem of diffusive signal dilution can be addressed by designing a probe that upon enzyme conversion releases a fluorophore that precipitates. An excited-state intramolecular proton transfer (ESIPT)-based solid-state fluorophore HTPQ was developed that is strictly insoluble in water and emits intense fluorescence in the solid state, with λex/em =410/550 nm, thus making it far better suited to use with a commercial confocal microscope. HTPQ was further utilized in the design of an enzyme-responsive, fluorogenic probe (HTPQA), targeting alkaline phosphatase (ALP) as a model enzyme. HTPQA makes possible diffusion-resistant in situ detection of endogenous ALP in live cells. It was also employed in the visualizing of different levels of ALP in osteosarcoma cells and tissue, thus demonstrating its interest for the diagnosis of this type of cancer.
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