生物正交化学
荧光
化学
四嗪
叠氮化物
生物物理学
光化学
纳米技术
点击化学
组合化学
材料科学
有机化学
量子力学
生物
物理
作者
Youyong Yuan,Shidang Xu,Xiamin Cheng,Xiaolei Cai,Bin Liu
标识
DOI:10.1002/anie.201601744
摘要
Abstract Bioorthogonal turn‐on probes have been widely utilized in visualizing various biological processes. Most of the currently available bioorthogonal turn‐on probes are blue or green emissive fluorophores with azide or tetrazine as functional groups. Herein, we present an alternative strategy of designing bioorthogonal turn‐on probes based on red‐emissive fluorogens with aggregation‐induced emission characteristics (AIEgens). The probe is water soluble and non‐fluorescent due to the dissipation of energy through free molecular motion of the AIEgen, but the fluorescence is immediately turned on upon click reaction with azide‐functionalized glycans on cancer cell surface. The fluorescence turn‐on is ascribed to the restriction of molecular motion of AIEgen, which populates the radiative decay channel. Moreover, the AIEgen can generate reactive oxygen species (ROS) upon visible light ( λ =400–700 nm) irradiation, demonstrating its dual role as an imaging and phototherapeutic agent.
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