Rationally designed an innovative proximity labeling near-infrared fluorogenic probe for imaging of peroxynitrite in acute lung injury

过氧亚硝酸盐 一氧化氮 氧化应激 活性氧 荧光寿命成像显微镜 生物物理学 荧光 发病机制 化学 细胞生物学 医学 病理 生物化学 生物 物理 量子力学 有机化学 超氧化物 体内 生物技术
作者
Dandan Tang,Ningge Xu,Yuyang Fu,Wei Peng,Jinsheng Wu,Heng Liu,Fabiao Yu
出处
期刊:Chinese Chemical Letters [Elsevier BV]
卷期号:36 (5): 110082-110082 被引量:18
标识
DOI:10.1016/j.cclet.2024.110082
摘要

Acute lung injury (ALI) is a serious clinical condition with a high mortality rate. Oxidative stress and inflammatory responses play pivotal roles in the pathogenesis of ALI. ONOO− is a key mediator that exacerbates oxidative damage and microvascular permeability in ALI. Accurate detection of ONOO− would facilitate early diagnosis and intervention in ALI. Near-infrared fluorescence (NIRF) probes offer new solutions due to their sensitivity, depth of tissue penetration, and imaging capabilities. However, the developed ONOO− fluorescent probes face problems such as interference from other reactive oxygen species and easy intracellular diffusion. To address these issues, we introduced an innovative self-immobilizing NIRF probe, DCI2F-OTf, which was capable of monitoring ONOO− in vitro and in vivo. Importantly, leveraging the high reactivity of the methylene quinone (QM) intermediate, DCI2F-OTf was able to covalently label proteins in the presence of ONOO−, enabling in situ imaging. In mice models of ALI, DCI2F-OTf enabled real-time imaging of ONOO− levels and found that ONOO− was tightly correlated with the progression of ALI. Our findings demonstrated that DCI2F-OTf was a promising chemical tool for the detection of ONOO−, which could help to gain insight into the pathogenesis of ALI and monitor treatment efficacy.
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