Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA 94143, USA; Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94143, USA.
Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94143, USA.
Mol Cell. 2018 Jan 18;69(2):334-346.e4. doi: 10.1016/j.molcel.2017.12.008. Epub 2018 Jan 4.
Visualizing dynamics of kinase activity in living animals is essential for mechanistic understanding of cell and developmental biology. We describe GFP-based kinase reporters that phase-separate upon kinase activation via multivalent protein-protein interactions, forming intensively fluorescent droplets. Called SPARK (separation of phases-based activity reporter of kinase), these reporters have large dynamic range (fluorescence change), high brightness, fast kinetics, and are reversible. The SPARK-based protein kinase A (PKA) reporter reveals oscillatory dynamics of PKA activities upon G protein-coupled receptor activation. The SPARK-based extracellular signal-regulated kinase (ERK) reporter unveils transient dynamics of ERK activity during tracheal metamorphosis in live Drosophila. Because of intensive brightness and simple signal pattern, SPARKs allow easy examination of kinase signaling in living animals in a qualitative way. The modular design of SPARK will facilitate development of reporters of other kinases.
在活生物体中可视化激酶活性的动态对于理解细胞和发育生物学的机制至关重要。我们描述了基于 GFP 的激酶报告子,它们通过多价蛋白质-蛋白质相互作用在激酶激活时相分离,形成密集荧光的液滴。这些报告子称为 SPARK(基于相分离的激酶活性报告子),具有大的动态范围(荧光变化)、高亮度、快速动力学和可逆性。基于 SPARK 的蛋白激酶 A(PKA)报告子揭示了 G 蛋白偶联受体激活时 PKA 活性的振荡动力学。基于 SPARK 的细胞外信号调节激酶(ERK)报告子揭示了活体果蝇气管变态过程中 ERK 活性的短暂动力学。由于亮度高且信号模式简单,SPARK 允许以定性方式轻松检查活生物体中的激酶信号。SPARK 的模块化设计将有助于开发其他激酶的报告子。