Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan.
J Am Chem Soc. 2013 Aug 21;135(33):12360-5. doi: 10.1021/ja405745v. Epub 2013 Aug 8.
We developed novel fluorogenic probes for no-wash live-cell imaging of proteins fused to PYP-tag, which is a small protein tag recently reported by our group. Through the design of a new PYP-tag ligand, specific intracellular protein labeling with rapid kinetics and fluorogenic response was accomplished. The probes crossed the cell membrane, and cytosolic and nuclear localizations of PYP-tagged proteins without cell washing were visualized within a 6-min reaction time. The fluorogenic response was due to the environmental effect of fluorophore upon binding to PYP-tag. Furthermore, the PYP-tag-based method was applied to the imaging of methyl-CpG-binding domain localization. This rapid protein-labeling system combined with the small protein tag and designed fluorogenic probes offers a powerful method to study the localization, movement, and function of cellular proteins.
我们开发了新型荧光探针,可用于无洗涤活细胞中融合了 PYP 标签的蛋白质成像,PYP 标签是我们小组最近报道的一种小蛋白标签。通过设计新的 PYP 标签配体,实现了具有快速动力学和荧光响应的特异性细胞内蛋白质标记。探针穿过细胞膜,在 6 分钟的反应时间内无需洗涤即可可视化 PYP 标记蛋白的细胞质和核定位。荧光响应是由于荧光团与 PYP 标签结合时的环境效应。此外,基于 PYP 标签的方法还应用于甲基-CpG 结合域定位的成像。这种快速的蛋白质标记系统结合了小蛋白标签和设计的荧光探针,为研究细胞蛋白质的定位、运动和功能提供了一种强大的方法。