化学
蛋白质标签
表位
细胞生物学
荧光
活体细胞成像
荧光寿命成像显微镜
绿色荧光蛋白
计算生物学
荧光蛋白
生物物理学
突变体
细胞内
蛋白质亚细胞定位预测
肽
荧光显微镜
亮度
线性表位
黄色荧光蛋白
分子成像
靶蛋白
表位定位
HEK 293细胞
蛋白质-蛋白质相互作用
蛋白质工程
内生
分子生物学
作者
Li‐Chun Tu,Hong Qin,Siyuan Luo,Xiaofei Liu,Ruikang Zhao,Xiangyan Ding,Shuyi Zhang,Ling Chu
摘要
Epitope tags, or peptide tags, are ideal genetically encodable labels for super-resolution imaging due to their compact size. However, their application in live-cell super-resolution imaging of intracellular proteins has been limited by low labeling specificity and efficiency. To address this limitation, we developed the ligand-induced self-complementing tag (LiSC-tag) as a novel epitope tag for live-cell super-resolution imaging and the functional manipulation of cellular proteins. The LiSC-tag utilizes a split FKBP mutant that self-complements upon the addition of small-molecule fluorescent probes. It integrates the compact size of epitope tags with the high brightness and photostability of small-molecule dyes, enabling multicolor nanoscopy imaging using STED, STORM, and SIM. The LiSC-tag exhibits improved brightness and photostability relative to split fluorescent proteins. It is compatible with endogenous protein imaging and can be engineered in tandem arrays to enhance fluorescence signals. Beyond imaging, the LiSC-tag also enables the manipulation of protein localization and targeted protein degradation.
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