Two-Photon Cellular and Intravital Imaging of Hypochlorous Acid by Fluorescent Probes That Exhibit a Synergistic Excited-State Intramolecular Proton Transfer–Intramolecular Charge Transfer Mechanism Enabling Near-Infrared Emission with a Large Stokes Shift

化学 分子内力 次氯酸 荧光 光化学 质子 激发态 双光子激发显微术 电荷(物理) 红外线的 原子物理学 立体化学 光学 有机化学 物理 量子力学
作者
Ying Long,Junru Liu,Zhenghua Ju,Fujian Qi,Wei Tang,Shuai Yan,Fang Dai,Shengxiang Zhang,Bo Zhou
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:96 (45): 18104-18112 被引量:12
标识
DOI:10.1021/acs.analchem.4c04075
摘要

To develop highly effective molecular tools for intravital imaging of hypochlorous acid (HOCl), in this study, we initially designed two-photon hybrid fluorophores, SDP and P-SDP, by conjugating the classical dye 2-(2′-hydroxyphenyl)benzothiazole with the two-photon hydroxylphenyl-butadienylpyridinium fluorophore. The designed fluorophores exhibit a synergistic interaction between excited-state intramolecular proton transfer and intramolecular charge transfer mechanisms, enabling near-infrared (NIR) emission and significant Stokes shifts. Subsequently, using these fluorophores, we developed two HOCl fluorescent probes, SDP-SN and P-SDP-SN, by further incorporating N,N-dimethylthiocarbamate as a specific recognition group for HOCl. Toward HOCl, both SDP-SN and P-SDP-SN demonstrate an ultrafast response (less than 3 s), NIR emission at wavelengths of 714 and 682 nm, and remarkable Stokes shifts of 303 and 271 nm, respectively. Leveraging these advantages in conjunction with their ability to cross the blood–brain barrier, the probes find successful application in two-photon cellular and intravital imaging of HOCl. This includes visualizing endogenous generation of HOCl in cellular models related to inflammation, hyperglycemia, and ferroptosis, as well as mapping in vivo generation of HOCl within the brain and abdominal cavity using a murine model of systemic inflammation.
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