Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-Ku, Kyoto 615-8510 (Japan), Fax: (+81) 75-383-2759.
Chemistry. 2013 Sep 16;19(38):12875-83. doi: 10.1002/chem.201300817. Epub 2013 Aug 16.
Specific turn-on detection of enzyme activities is of fundamental importance in drug discovery research, as well as medical diagnostics. Although magnetic resonance imaging (MRI) is one of the most powerful techniques for noninvasive visualization of enzyme activity, both in vivo and ex vivo, promising strategies for imaging specific enzymes with high contrast have been very limited to date. We report herein a novel signal-amplifiable self-assembling (19) F NMR/MRI probe for turn-on detection and imaging of specific enzymatic activity. In NMR spectroscopy, these designed probes are "silent" when aggregated, but exhibit a disassembly driven turn-on signal change upon cleavage of the substrate part by the catalytic enzyme. Using these (19) F probes, nanomolar levels of two different target enzymes, nitroreductase (NTR) and matrix metalloproteinase (MMP), could be detected and visualized by (19) F NMR spectroscopy and MRI. Furthermore, we have succeeded in imaging the activity of endogenously secreted MMP in cultured media of tumor cells by (19) F MRI, depending on the cell lines and the cellular conditions. These results clearly demonstrate that our turn-on (19) F probes may serve as a screening platform for the activity of MMPs.
特定酶活性的开启检测在药物发现研究以及医学诊断中具有重要意义。尽管磁共振成像(MRI)是用于在体内和体外非侵入性可视化酶活性的最强大技术之一,但迄今为止,用于对特定酶进行高对比度成像的有前景的策略非常有限。我们在此报告了一种用于特定酶活性的开启检测和成像的新型信号放大自组装(19)F NMR/MRI 探针。在 NMR 光谱学中,这些设计的探针在聚集时是“沉默的”,但在被催化酶切割后,其底物部分的分解会导致开启信号发生变化。使用这些(19)F 探针,通过(19)F NMR 光谱和 MRI 可以检测和可视化两种不同靶酶,即硝基还原酶(NTR)和基质金属蛋白酶(MMP)的纳米摩尔水平。此外,我们已经成功地通过(19)F MRI 对肿瘤细胞培养介质中内源性分泌的 MMP 活性进行成像,这取决于细胞系和细胞状态。这些结果清楚地表明,我们的开启(19)F 探针可以作为 MMP 活性的筛选平台。