生物结合
荧光
深铬移
荧光寿命成像显微镜
纳米技术
生物成像
化学
荧光显微镜
显微镜
材料科学
吸收(声学)
量子点
生物物理学
组合化学
斯托克斯位移
分子成像
显像剂
体内分布
生物分子
作者
Diego Abad-Montero,Manel Bosch,Rodrigo Garcés‐Castellanos,Michael Q. Schottenhamel,Sergio Pedraza‐Arévalo,Alejandro Ibáñez‐Costa,Justo P. Castaño,Tania Garcia‐Becerra,Elena Rebollo,Marta E. Alberto,Antonio Francés‐Monerris,Vicente Marchán
摘要
Fluorescent probes operating in the near-infrared (NIR) region offer deep-tissue visualization with minimal background interference, reduced phototoxicity, and enhanced signal-to-noise ratios. However, most conventional NIR fluorophores exhibit poor photostability, low fluorescence quantum yields, and limited chemical versatility, which constrain their use in demanding biological environments. Here, we report a new family of π-extended COUPY dyes (3-7), rationally engineered to deliver efficient far-red/NIR performance through vinylogation of the exocyclic double bond of the coumarin scaffold. This single structural modification induces a bathochromic shift exceeding 100 nm in both absorption and emission spectra while preserving the compact architecture and synthetic accessibility of the parent coumarin. The resulting dyes combine high molar absorptivity, moderate-to-high quantum yields, and exceptional photostability under biologically-relevant conditions. Their performance was validated in live-cell imaging using both intensity-based and fluorescence lifetime imaging microscopy (FLIM), demonstrating compatibility with advanced imaging techniques. Furthermore, site-specific bioconjugation to a clinically relevant peptide confirmed their suitability for targeted imaging. Collectively, π-extended COUPY dyes represent a promising class of synthetically modular, chemically robust, and biologically compatible far-red/NIR fluorophores for high-resolution imaging, targeted strategies, and advanced bioimaging modalities, and provide a foundation for future studies aimed at evaluating their performance in more complex biological models.
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