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通过激酶导向底物筛选(KIOSS)对蛋白激酶底物进行体内鉴定。

In Vivo Identification of Protein Kinase Substrates by Kinase-Oriented Substrate Screening (KIOSS).

作者信息

Nishioka Tomoki, Amano Mutsuki, Funahashi Yasuhiro, Tsuboi Daisuke, Yamahashi Yukie, Kaibuchi Kozo

机构信息

Department of Cell Pharmacology, Graduate School of Medicine, Nagoya University, Nagoya, Japan.

出版信息

Curr Protoc Chem Biol. 2019 Mar;11(1):e60. doi: 10.1002/cpch.60. Epub 2019 Jan 7.

Abstract

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.

摘要

蛋白质磷酸化在细胞功能调控中起着关键作用。有关蛋白质磷酸化及相关激酶的信息对于理解细胞内信号传导至关重要。一种名为KIOSS(激酶导向底物筛选)的体内激酶底物筛选方法已被开发出来。本方案提供了一种利用诸如14-3-3蛋白、pin1-WW结构域和chek2-FHA结构域等磷蛋白结合模块作为生物过滤器的方法,以成功富集与细胞内信号传导相关的磷酸化蛋白,而非管家蛋白和/或结构蛋白。通过该方法已在HeLa细胞中鉴定出超过1000种PKA、PKC、MAPK和Rho激酶的底物候选物,以及在小鼠脑片培养物中D1R、NMDAR、腺苷A2a受体、PKA、PKC、MAPK和Rho激酶下游的磷酸化情况。一个名为KANPHOS(激酶相关神经磷酸信号)的在线数据库提供了这些研究鉴定出的磷酸化信号,以及文献中先前报道的信号。© 2019约翰威立国际出版公司。

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