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利用高斯荧光素酶对活的哺乳动物细胞中的蛋白质分泌途径进行实时生物发光成像。

Real-time bioluminescence imaging of a protein secretory pathway in living mammalian cells using Gaussia luciferase.

作者信息

Suzuki Takahiro, Usuda Shinsuke, Ichinose Hiroshi, Inouye Satoshi

机构信息

Faculty of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama 226-8501, Japan.

出版信息

FEBS Lett. 2007 Oct 2;581(24):4551-6. doi: 10.1016/j.febslet.2007.08.036. Epub 2007 Aug 27.

Abstract

Using photon counting and charge-coupled device (CCD) cameras, we have applied the method of real-time bioluminescence imaging to investigate protein trafficking in mammalian cells. In the living cells of Chinese hamster ovary and PC12D cells, exocytotic secretion of protein and protein targeting on the cell surface were visualized using the secreted Gaussia luciferase (GLase) as a reporter protein in a minute. After incubation of the cells with luciferin (coelenterazine) for 10min, luciferin was imported into the cells and the vesicle transport network in the cells could be shown by luminescence images of GLase activity. Further, we demonstrate that GLase with a heterologous signal peptide sequence is targeted to the cell surface in neuronally differentiated PC12D cells and luminescence signals could be detected in a few seconds.

摘要

我们使用光子计数和电荷耦合器件(CCD)相机,应用实时生物发光成像方法来研究哺乳动物细胞中的蛋白质运输。在中国仓鼠卵巢细胞和PC12D细胞的活细胞中,使用分泌型高斯荧光素酶(GLase)作为报告蛋白,在数分钟内就可观察到蛋白质的胞吐分泌以及蛋白质在细胞表面的靶向定位。在用荧光素(腔肠素)孵育细胞10分钟后,荧光素被导入细胞,通过GLase活性的发光图像可以显示细胞内的囊泡运输网络。此外,我们证明带有异源信号肽序列的GLase在神经分化的PC12D细胞中靶向细胞表面,并且在几秒钟内就可以检测到发光信号。

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