Sato Moritoshi, Umezawa Yoshio
Graduate School of Arts and Sciences, The University of Tokyo, Komaba, Meguro-ku, Tokyo, 153-8902, Japan.
Department of Chemistry, School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Methods Mol Biol. 2016;1360:149-56. doi: 10.1007/978-1-4939-3073-9_11.
Protein phosphorylation by intracellular kinases plays one of the most pivotal roles in signaling pathways within cells. To reveal the biological processes related to the kinase proteins, electrophoresis, immunocytochemistry, and in vitro kinase assay have been used. However, these conventional methods do not provide enough information about spatial and temporal dynamics of the signal transduction based on protein phosphorylation and dephosphorylation in living cells. To overcome the limitation for investigating the kinase signaling, we developed genetically encoded fluorescent indicators for visualizing the protein phosphorylation in living cells. Using these indicators, we visualized under a fluorescence microscope when, where, and how the protein kinases are activated in single living cells.
细胞内激酶介导的蛋白质磷酸化在细胞信号通路中发挥着最为关键的作用之一。为了揭示与激酶蛋白相关的生物学过程,人们采用了电泳、免疫细胞化学和体外激酶测定等方法。然而,这些传统方法无法提供足够的信息,以了解活细胞中基于蛋白质磷酸化和去磷酸化的信号转导的时空动态。为了克服研究激酶信号传导的局限性,我们开发了基因编码荧光指示剂,用于在活细胞中可视化蛋白质磷酸化。利用这些指示剂,我们在荧光显微镜下观察到了单个活细胞中蛋白激酶何时、何地以及如何被激活。