Fukano Takashi, Sawano Asako, Ohba Yusuke, Matsuda Michiyuki, Miyawaki Atsushi
Laboratory for Cell Function and Dynamics, Advanced Technology Development Center, Brain Science Institute, RIKEN.
Cell Struct Funct. 2007;32(1):9-15. doi: 10.1247/csf.06019. Epub 2007 Feb 21.
Although the consequences of Ras activation have been studied extensively in the context of oncogenesis, its regulation in physiological modes of signal transduction is not well understood. A fluorescent indicator, Raichu-Ras, was fused to the C-terminal hypervariable regions of H-Ras and K-Ras to create indicators for Ras activation within caveolae/rafts (Raichu-tH) and non-raft domains (Raichu-tK) of the plasma membrane, respectively. Raichu-tH was also found abundantly in endomembranes. To monitor Ras activation with high spatial resolution, it is imperative to observe sectioned images of the signals. We have developed a wide-field fluorescence microscope equipped with a digital micromirror device (DMD) to acquire optically sectioned images using fringe projection. This system provides reliable signals from fluorescence resonance energy transfer (FRET) between cyan and yellow mutants of green fluorescent protein. We have used this system to demonstrate that, upon stimulation with growth factors, the two indicators are activated in spatially and temporally unique patterns.
尽管在肿瘤发生的背景下,Ras激活的后果已得到广泛研究,但其在生理信号转导模式中的调控仍未得到充分理解。一种荧光指示剂Raichu-Ras与H-Ras和K-Ras的C端高变区融合,分别创建了用于检测质膜小窝/脂筏(Raichu-tH)和非脂筏结构域(Raichu-tK)内Ras激活的指示剂。Raichu-tH在内膜中也大量存在。为了以高空间分辨率监测Ras激活,观察信号的切片图像至关重要。我们开发了一种配备数字微镜器件(DMD)的宽场荧光显微镜,以利用条纹投影获取光学切片图像。该系统提供了来自绿色荧光蛋白青色和黄色突变体之间荧光共振能量转移(FRET)的可靠信号。我们使用该系统证明,在用生长因子刺激后,这两种指示剂以空间和时间上独特的模式被激活。