TY - JOUR
T1 - In Vivo Identification of Protein Kinase Substrates by Kinase-Oriented Substrate Screening (KIOSS)
AU - Nishioka, Tomoki
AU - Amano, Mutsuki
AU - Funahashi, Yasuhiro
AU - Tsuboi, Daisuke
AU - Yamahashi, Yukie
AU - Kaibuchi, Kozo
N1 - Publisher Copyright:
© 2019 John Wiley & Sons, Inc.
PY - 2019/3/1
Y1 - 2019/3/1
N2 - 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.
AB - 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.
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U2 - 10.1002/cpch.60
DO - 10.1002/cpch.60
M3 - Article
C2 - 30615307
AN - SCOPUS:85061996566
SN - 2160-4762
VL - 11
SP - e60
JO - Current protocols in chemical biology
JF - Current protocols in chemical biology
IS - 1
ER -