体内
荧光
荧光寿命成像显微镜
化学
磁共振成像
共价键
生物物理学
原位
融合蛋白
酶
临床前影像学
生物化学
重组DNA
生物
光学
物理
放射科
生物技术
有机化学
基因
医学
作者
Yu Qiao,Lei Zhang,Mou Jiang,Long Xiao,Yunhui Xiang,Ruifang Wang,Zhao‐Qing Liu,Rui Zhou,Minghui Yang,Conggang Li,Maili Liu,Xin Zhou,Shizhen Chen
标识
DOI:10.1002/anie.202313137
摘要
To realize sensing and labeling biomarkers is quite challenging in terms of designing multimodal imaging probes. In this study, we developed a novel β-galactosidase (β-gal) activated bimodal imaging probe that combines near-infrared (NIR) fluorescence and magnetic resonance imaging (MRI) to enable real-time visualization of activity in living organisms. Upon β-gal activation, Gal-Cy-Gd-1 exhibits a remarkable 42-fold increase in NIR fluorescence intensity at 717 nm, allowing covalent labeling of adjacent target enzymes or proteins and avoiding molecular escape to promote probe accumulation at the tumor site. This fluorescence reaction enhances the longitudinal relaxivity by approximately 1.9 times, facilitating high-resolution MRI. The unique features of Gal-Cy-Gd-1 enable real-time and precise visualization of β-gal activity in live tumor cells and mice. The probe's utilization aids in identifying in situ ovarian tumors, offering valuable assistance in the precise removal of tumor tissue during surgical procedures in mice. The fusion of NIR fluorescence and MRI activation through self-immobilizing target enzymes or proteins provides a robust approach for visualizing β-gal activity. Moreover, this approach sets the groundwork for developing other activatable bimodal probes, allowing real-time in vivo imaging of enzyme activity and localization.
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