Specific Cell Surface Protein Imaging by Extended Self-Assembling Fluorescent Turn-on Nanoprobes

被引:151
作者
Mizusawa, Keigo [1 ]
Takaoka, Yousuke [1 ]
Hamachi, Itaru [1 ,2 ]
机构
[1] Kyoto Univ, Dept Synthet Chem & Biol Chem, Nishikyo Ku, Kyoto 6158510, Japan
[2] Japan Sci & Technol Agcy JST, CREST, Chiyoda Ku, Tokyo 1020075, Japan
基金
日本科学技术振兴机构;
关键词
CARBONIC-ANHYDRASE-IX; CANCER-CELLS; DIHYDROFOLATE-REDUCTASE; FOLATE RECEPTOR; DESIGN; INHIBITORS; EXPRESSION; PROBE; PH; NANOPARTICLES;
D O I
10.1021/ja304239g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Visualization of tumor-specific protein biomarkers on cell membranes has the potential to contribute greatly to basic biological research and therapeutic applications. We recently reported a unique supramolecular strategy for specific protein detection using self-assembling fluorescent nanoprobes consisting of a hydrophilic protein ligand and a hydrophobic BODIPY fluorophore in test tube settings. This method is based on recognition-driven disassembly of the nanoprobes, which induces a clear turn-on fluorescent signal. In the present study, we have successfully extended the range of applicable fluorophores to the more hydrophilic ones such as fluorescein or rhodamine by introducing a hydrophobic module near the fluorophore. Increasing the range of available fluorophores allowed selective imaging of membrane-bound proteins under live cell conditions. That is, overexpressed folate receptor (FR) or hypoxia-inducible membrane-bound carbonic anhydrases (CA) on live cell surfaces as cancer-specific biomarkers were fluorescently visualized using the designed supramolecular nanoprobes in the turn-on manner. Moreover, a cell-based inhibitor-assay platform for CA on a live cell surface was constructed, highlighting the potential applicability of the self-assembling turn-on probes.
引用
收藏
页码:13386 / 13395
页数:10
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