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通过扩展自组装荧光开启纳米探针对特定细胞表面蛋白进行成像。

Specific cell surface protein imaging by extended self-assembling fluorescent turn-on nanoprobes.

机构信息

Department of Synthetic Chemistry and Biological Chemistry, Kyoto University, Katsura, Nishikyo-Ku, Kyoto 615-8510, Japan.

出版信息

J Am Chem Soc. 2012 Aug 15;134(32):13386-95. doi: 10.1021/ja304239g. Epub 2012 Aug 7.

Abstract

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.

摘要

细胞膜上肿瘤特异性蛋白生物标志物的可视化有可能对基础生物学研究和治疗应用做出重大贡献。我们最近报道了一种独特的超分子策略,用于使用由亲水蛋白配体和疏水 BODIPY 荧光团组成的自组装荧光纳米探针在试管环境中进行特定蛋白质检测。该方法基于纳米探针的识别驱动解组装,这会诱导明显的荧光信号开启。在本研究中,我们通过在荧光团附近引入疏模块,成功地将适用的荧光团范围扩展到更亲水的荧光团,如荧光素或罗丹明。增加可用荧光团的范围使得可以在活细胞条件下选择性地对膜结合蛋白进行成像。也就是说,使用设计的超分子纳米探针以开启方式对活细胞表面上过表达的叶酸受体 (FR) 或缺氧诱导的膜结合碳酸酐酶 (CA) 等作为癌症特异性生物标志物进行荧光可视化。此外,构建了用于活细胞表面上 CA 的基于细胞的抑制剂测定平台,突出了自组装开启探针的潜在适用性。

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