Systematic investigation of protein kinase A substrate proteins using on-chip protein kinase kinetic profiling. Issue 12 (24th May 2017)

• Record Type: Journal Article
• Authors: Jung, Se-Hui; Kong, Deok-Hoon; Jeon, Hye-Yoon; Han, Eun-Taek; Park, Won Sun; Hong, Seok-Ho; Kim, Young-Myeong; Ha, Kwon-Soo
• Is Part Of: Analyst. Volume 142:Issue 12(2017)
• Page Start: 2239
• Page End: 2246
• Publication Date: 2017-05-24
• Subjects: Chemistry, Analytic -- Periodicals; 543
• DOI: 10.1039/c6an02682f
• Languages: English
• ISSNs: 0003-2654

Abstract

Abstract : An on-chip protein kinase assay for profiling kinase kinetic parameters by introducing the substrate affinity ( K m ) and the phosphorylation rate ( V p ) under physiological conditions. Abstract : Protein kinases play a critical role in a wide variety of cellular processes through post-translational protein phosphorylation and identification of their substrate proteins is important for understanding the enzymes' mechanism of action and elucidating their functions in physiological and disease processes. However, there have been few systematic investigations of protein kinase substrates due to a lack of high-throughput kinetic assays. Thus, we designed an on-chip protein kinase assay for profiling kinase kinetic parameters by introducing the phosphorylation rate ( V p ) under physiological conditions, instead of the maximal velocity ( V max ), in a high-throughput manner. We applied this method to the kinetic analysis of protein kinase A (PKA) for 28 nuclear, cytosolic, plasma membrane, and extracellular target proteins to determine the substrate affinity ( K m ), V p (FIATP10 /s), and substrate preference ( V p / K m ). We then constructed a map of PKA's kinetic parameters with respect to the 28 proteins based on subcellular localization. Thus, the on-chip protein kinase kinetic profiling is an ideal approach for systematically investigating substrate proteins of protein kinases and fully characterizing the enzymes' physiological functions.