Esaki Tsuyoshi, Masujima Tsutomu
Quantitative Biology Center (QBiC), RIKEN.
Anal Sci. 2015;31(12):1211-3. doi: 10.2116/analsci.31.1211.
Mitochondria in a live HepG2 cell were visualized with a fluorescent probe to specify their location and state in a living cell. Then, mitochondria were selectively captured with a nanospray tip under fluorescence microscope, and thousands of small molecular peaks were revealed and unique steroids specific to mitochondria were also found. This fluorescence imaging combined with live single-cell mass spectrometry opens the door to the analysis of site- and state-specific molecular detection to elucidate precise molecular mechanisms at the single-cell and organelle level.
使用荧光探针观察活的HepG2细胞中的线粒体,以确定它们在活细胞中的位置和状态。然后,在荧光显微镜下用纳米喷雾尖端选择性捕获线粒体,揭示了数千个小分子峰,还发现了线粒体特有的独特类固醇。这种荧光成像与活细胞单细胞质谱联用,为在单细胞和细胞器水平上分析位点和状态特异性分子检测以阐明精确的分子机制打开了大门。