| Literature DB >> 34270059 |
Jiahui Wang1, Xiaolin Yang2, Lin Xi1, Xu Na Wu3.
Abstract
Phosphorylation of a substrate by protein kinases leads to the activation or inactivation of numerous signaling pathways and metabolic processes. The assessment of kinase activity by using a specific or generic substrate plays a crucial role in characterization of kinase specificity and activity. Here we describe a protocol using either a synthetic peptide as a specific substrate or using myelin basic protein (MBP) as a generic substrate for the kinase activity assay. The kinase of interest is fused with a GFP (green fluorescent protein) tag and can be purified by GFP magnetic beads. Kinase-GFP complexes are then incubated with ATP, substrate, and coordinated reaction reagent for the kinase reaction. The assay is then quantified through mass spectrometry or enzymatic luminescence.Entities:
Keywords: Enzymatic luminescence; Kinase substrates; Magnetic Kinase-GFP purification; Mass spectrometry; Phosphorylation detection
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Year: 2021 PMID: 34270059 DOI: 10.1007/978-1-0716-1625-3_17
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745