系统间交叉
荧光
吡啶
分子内力
光化学
化学
聚集诱导发射
接受者
费斯特共振能量转移
生物物理学
分析化学(期刊)
色谱法
光学
激发态
立体化学
物理
凝聚态物理
生物
单重态
核物理学
药物化学
作者
Hanchen Shen,Lidong Du,Changhuo Xu,Bingzhe Wang,Qingqing Zhou,Ruquan Ye,Ryan T. K. Kwok,Jacky W. Y. Lam,Guichuan Xing,Jianwei Sun,Tzu‐Ming Liu,Ben Zhong Tang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-07-26
卷期号:18 (31): 20268-20282
标识
DOI:10.1021/acsnano.4c03963
摘要
Activity-based detection of γ-Glutamyltranspeptidase (GGT) using near-infrared (NIR) fluorescent probes is a promising strategy for early cancer diagnosis. Although NIR pyridinium probes show high performance in biochemical analysis, the aggregation of both the probes and parental fluorochromes in biological environments is prone to result in a low signal-to-noise ratio (SBR), thus affecting their clinical applications. Here, we develop a GGT-activatable aggregate probe called OTBP-G for two-photon fluorescence imaging in various biological environments under 1040 nm excitation. By rationally tunning the hydrophilicity and donor-acceptor strength, we enable a synergistic effect between twisted intramolecular charge transfer and intersystem crossing processes and realize a perfect dark state for OTBP-G before activation. After the enzymatic reaction, the parental fluorochrome exhibits bright aggregation-induced emission peaking at 670 nm. The fluorochrome-to-probe transformation can induce 1000-fold fluorescence ON/OFF ratio, realizing
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