| Literature DB >> 30615307 |
Tomoki Nishioka1, Mutsuki Amano1, Yasuhiro Funahashi1, Daisuke Tsuboi1, Yukie Yamahashi1, Kozo Kaibuchi1.
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.Entities:
Keywords: interactome; kinase; mass spectrometry; phosphoproteomics; phosphorylation
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Year: 2019 PMID: 30615307 DOI: 10.1002/cpch.60
Source DB: PubMed Journal: Curr Protoc Chem Biol ISSN: 2160-4762