Feng Bin, Chu Feiyi, Fang Yanpeng, Liu Min, Feng Xueping, Dong Jie, Chen Fei, Zeng Wenbin
Xiangya School of Pharmaceutical Sciences, Central South University Changsha 410013 China
Hunan Key Laboratory of Diagnostic and Therapeutic Drug Research for Chronic Diseases Changsha 410013 China.
Chem Sci. 2024 Apr 16;15(19):7324-7331. doi: 10.1039/d4sc00487f. eCollection 2024 May 15.
To facilitate the understanding of the dynamic distribution and activity of lysosomal enzymes, it is highly desirable to develop high-fidelity near-infrared (NIR) activatable fluorescent probes. Here, we propose a general acceptor engineering strategy to construct NIR probes with lysosome-targeting capability. Upon isosteric replacement and additional functionalization, the β-gal-activatable probe OELyso-Gal exhibited excellent lysosome-targeting capability and favorable responsive performance to the enzyme of interest. Notably, the steric hindrance effect from acceptor engineering is modest, which renders the probe unprecedented affinity to enzymes. Upon the introduction of acceptor engineering, the lysosome-targeting probe became more sensitive to β-gal in cells and tissues, boosting the discrimination of high β-gal-expressing ovarian cancer tumours from low β-gal-expressing tissues. Furthermore, the superiority of OELyso-Gal was validated in real-time visualization of ovarian cancer in tumour-bearing mice. This elegant acceptor engineering strategy provides inspirational insights into the development of customized fluorescent probes for monitoring disease-associated biomarkers within subcellular organelles.
为了便于理解溶酶体酶的动态分布和活性,开发高保真近红外(NIR)可激活荧光探针是非常必要的。在此,我们提出一种通用的受体工程策略来构建具有溶酶体靶向能力的近红外探针。通过等排取代和额外的功能化修饰,β-半乳糖苷酶可激活探针OELyso-Gal表现出优异的溶酶体靶向能力以及对目标酶良好的响应性能。值得注意的是,受体工程产生的空间位阻效应适中,这使得该探针对酶具有前所未有的亲和力。引入受体工程后,溶酶体靶向探针在细胞和组织中对β-半乳糖苷酶变得更加敏感,增强了高表达β-半乳糖苷酶的卵巢癌肿瘤与低表达β-半乳糖苷酶组织之间的区分度。此外,OELyso-Gal的优势在荷瘤小鼠卵巢癌的实时可视化中得到了验证。这种精妙的受体工程策略为开发定制荧光探针以监测亚细胞器内疾病相关生物标志物提供了启发性见解。