绿色荧光蛋白
细胞凋亡
细胞生物学
胞浆
化学
互补
斑马鱼
双分子荧光互补
荧光
线粒体
程序性细胞死亡
转染
多细胞生物
分子生物学
生物
细胞
生物化学
表型
基因
物理
酶
量子力学
作者
Yusuke Nasu,Yoshiyuki Asaoka,Misako Namae,Hiroshi Nishina,Hideyuki Yoshimura,Toshio Ozawa
标识
DOI:10.1021/acs.analchem.5b03367
摘要
Apoptosis plays a pivotal role in development and tissue homeostasis in multicellular organisms. Dysfunction of apoptosis is involved in many fatal diseases such as cancer. Visualization of apoptosis in living animals is necessary to understand the mechanism of apoptosis-related diseases. Here, we describe a genetically encoded fluorescent probe for imaging apoptosis in living multicellular organisms, based on spontaneous complementation of two fragments of a green fluorescent protein (GFP) variant (GFP OPT). The probe is designed for detection of mitochondria-mediated apoptosis during which a mitochondrial protein of Smac is released into cytosol. The Smac is connected with a carboxy-terminal fragment of GFP OPT (GFP11), whereas the remainder of GFP OPT (GFP(1-10)) is located in the cytosol. Under an apoptotic condition, the Smac is released from mitochondria into cytosol, allowing complementation of the GFP-OPT fragments and the emission of fluorescence. Live-cell imaging demonstrates that the probe enables detection of apoptosis in living cells with a high signal-to-background ratio. We applied the probe to living zebrafish, in which apoptotic cells were visualized with fluorescence. The technique provides a useful tool for the study of apoptosis in living animals, facilitating elucidation of the mechanisms of apoptosis-related diseases.
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