Department of Chemistry , The University of Hong Kong , Pokfulam Road , Hong Kong , China.
ACS Sens. 2019 May 24;4(5):1190-1196. doi: 10.1021/acssensors.8b01128. Epub 2019 May 6.
Small molecule-based fluorescent probes offer great opportunities for specifically tracking proteins in living systems with minimal perturbation on the protein function and localization. Herein, we report a small green fluorescent probe (Ni- NTA-AF) consisting of a Ni-NTA moiety, a fluorescein, and an arylazide group, that binds specifically to His-tagged proteins with fluorescence enhancement in vitro upon photoactivation of the arylazide group. Importantly, the probe can cross the cell membranes and stoichiometrically label His-tagged proteins rapidly (∼15 min) in living prokaryotic and eukaryotic cells exemplified by a DNA repair protein Xeroderma pigmentosum group A (XPA). Using the probe, we successfully visualized Sirtuin 5, which is localized to the mitochondria. This probe exhibits high quantum yields and improved solubility, offering a new opportunity for imaging intracellular His-tagged proteins inside living cells with better contrast.
基于小分子的荧光探针为在最小程度干扰蛋白质功能和定位的情况下特异性追踪活系统中的蛋白质提供了极好的机会。在此,我们报告了一种小分子绿色荧光探针(Ni-NTA-AF),它由 Ni-NTA 部分、荧光素和芳基叠氮基团组成,可特异性结合 His 标记的蛋白质,在芳基叠氮基团光激活后体外荧光增强。重要的是,该探针可以穿过细胞膜,并以化学计量比快速标记活原核和真核细胞中的 His 标记蛋白(以 DNA 修复蛋白 Xeroderma pigmentosum group A (XPA) 为例)。使用该探针,我们成功地可视化了定位于线粒体的 Sirtuin 5。该探针具有较高的量子产率和改善的溶解性,为在活细胞内对细胞内 His 标记蛋白进行成像提供了新的机会,对比度更好。