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Specific Detection and Imaging of Enzyme Activity by Signal‐Amplifiable Self‐Assembling 19F MRI Probes
Authors:Kazuya Matsuo  Dr Rui Kamada  Dr Keigo Mizusawa  Dr Hirohiko Imai  Dr Yuki Takayama  Dr Michiko Narazaki  Prof Dr Tetsuya Matsuda  Dr Yousuke Takaoka  Prof Dr Itaru Hamachi
Institution:1. 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;2. Department of System Science, Graduate School of Informatics, Kyoto University, 361‐1 Yoshida‐Honmachi, Sakyo‐ku, Kyoto 606‐8501 (Japan);3. Japan Science and Technology Agency (JST), CREST, 5 Sanbancho, Chiyoda‐ku, Tokyo 102‐0075 (Japan)
Abstract: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 19F 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 19F probes, nanomolar levels of two different target enzymes, nitroreductase (NTR) and matrix metalloproteinase (MMP), could be detected and visualized by 19F NMR spectroscopy and MRI. Furthermore, we have succeeded in imaging the activity of endogenously secreted MMP in cultured media of tumor cells by 19F MRI, depending on the cell lines and the cellular conditions. These results clearly demonstrate that our turn‐on 19F probes may serve as a screening platform for the activity of MMPs.
Keywords:enzyme activity  imaging agents  magnetic resonance imaging  NMR spectroscopy  self‐assembly  signal amplification
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