Development of optical probes with excellent intracellular retention

  • Kawatani Minoru
    Department of Life Science and Technology, Tokyo institution of Technology Graduate School of Medicine, The University of Tokyo
  • Kamiya Mako
    Department of Life Science and Technology, Tokyo institution of Technology
  • Urano Yasuteru
    Graduate School of Medicine, The University of Tokyo Graduate School of Pharmaceutical Science, The University of Tokyo

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  • 高い細胞内滞留性を有する光機能性プローブ群の開発
  • タカイ サイボウ ナイ タイリュウセイ オ ユウスル ヒカリ キノウセイ プローブグン ノ カイハツ

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Abstract

<p>Small-molecule based activatable fluorescence probes for detecting specific enzyme activity with high sensitivity can visualize the expression site of marker genes and cancers where the enzyme is highly expressed. However, the enzyme-catalyzed fluorescent hydrolysis product easily leaks out and diffuses from the reaction site, making it difficult to perform long-term tracking and immunohistochemical analysis which needs washing/fixation procedure. Our group have focused on quinone methide chemistry and developed series of activatable fluorescence probes with excellent intracellular retention that are converted to quinone-methide or aza-quinone-methide intermediates upon reaction with enzymes, which are then react with intracellular nucleophiles such as proteins and glutathione to be retained in cells and to exhibit significant increase in fluorescence. Based on this molecular design, we have developed fluorescence probes targeting β-galactosidase and γ-glutamyltranspeptidase with different colors. We also developed photo-functional probes such as activatable photosensitizers and caged fluorophores. These probes can visualize or kill target enzyme-expressing cells with high selectivity by suppressing the leakage of hydrolysis products from target cells, and fluorescence imaging in combination with immunostaining was possible due to the high tolerance of the obtained fluorescence signal even after washing and fixation.</p>

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