Literature DB >> 34270059

Kinase Activity Assay Using Unspecific Substrate or Specific Synthetic Peptides.

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.
© 2021. Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Enzymatic luminescence; Kinase substrates; Magnetic Kinase-GFP purification; Mass spectrometry; Phosphorylation detection

Mesh:

Substances:

Year:  2021        PMID: 34270059     DOI: 10.1007/978-1-0716-1625-3_17

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Comparison of SPA, FRET, and FP for kinase assays.

Authors:  Jinzi J Wu
Journal:  Methods Mol Biol       Date:  2002

Review 2.  Conveying endogenous and exogenous signals: MAPK cascades in plant growth and defense.

Authors:  Mengmeng Zhang; Jianbin Su; Yan Zhang; Juan Xu; Shuqun Zhang
Journal:  Curr Opin Plant Biol       Date:  2018-05-10       Impact factor: 7.834

  2 in total

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