激酶导向底物筛选(KIOSS)在体内鉴定蛋白激酶底物

Q3 Biochemistry, Genetics and Molecular Biology
Tomoki Nishioka, Mutsuki Amano, Yasuhiro Funahashi, Daisuke Tsuboi, Yukie Yamahashi, Kozo Kaibuchi
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引用次数: 10

摘要

蛋白磷酸化在细胞功能调控中起着至关重要的作用。蛋白质磷酸化和相关激酶的信息对于理解细胞内信号传导是重要的。一种名为KIOSS(激酶导向底物筛选)的激酶底物体内筛选方法已经被开发出来。该方案提供了一种方法,利用磷酸化蛋白结合模块,如14-3-3蛋白、pin1-WW结构域和chek2-FHA结构域作为生物过滤器,成功地富集与细胞内信号相关的磷酸化蛋白,而不是家政和/或结构蛋白。该方法鉴定了HeLa细胞中超过1000个PKA、PKC、MAPK和rho激酶候选底物,以及小鼠脑切片培养中D1R、NMDAR、腺苷A2a受体、PKA、PKC、MAPK和rho激酶的下游磷酸化。一个名为KANPHOS(激酶相关神经磷酸化信号)的在线数据库提供了这些研究鉴定的磷酸化信号,以及先前在文献中报道的磷酸化信号。©2019 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Vivo Identification of Protein Kinase Substrates by Kinase-Oriented Substrate Screening (KIOSS)

Protein phosphorylation plays a critical role in the regulation of cellular function. Information on protein phosphorylation and the responsible kinases is important for understanding intracellular signaling. A method for in vivo screening of kinase substrates named KIOSS (kinase-oriented substrate screening) has been developed. This protocol provides a method that utilizes phosphoprotein-binding modules such as 14-3-3 protein, the pin1-WW domain, and the chek2-FHA domain as biological filters to successfully enrich phosphorylated proteins related to intracellular signaling rather than housekeeping and/or structural proteins. More than 1000 substrate candidates for PKA, PKC, MAPK, and Rho-kinase in HeLa cells, as well as phosphorylation downstream of D1R, NMDAR, adenosine A2a receptor, PKA, PKC, MAPK, and Rho-kinase in mouse brain slice cultures have been identified by this method. An online database named KANPHOS (Kinase-Associated Neural Phospho-Signaling) provides the phosphorylation signals identified by these studies, as well as those previously reported in the literature. © 2019 by John Wiley & Sons, Inc.

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来源期刊
Current protocols in chemical biology
Current protocols in chemical biology Biochemistry, Genetics and Molecular Biology-Biophysics
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