Enhanced soluble production of biologically active recombinant human p38 mitogen-activated-protein kinase (MAPK) in Escherichia coli

Protein Pept Lett. 2007;14(8):756-60. doi: 10.2174/092986607781483660.

Abstract

The conditions were optimized for maximum soluble yield of biologically active recombinant p38alpha mitogen activated protein kinase (MAPK) vis-à-vis insoluble fraction (inclusion body formation). This study reports a rapid, economical and single step purification process for the overproduction of GST tagged p38alpha MAPK. A yield of 18 mg of highly purified and soluble protein per liter of bacterial culture within 6 h timeframe was achieved. The purified protein was found to be biologically suitable for phosphorylation by upstream kinases and was catalytically active. We further demonstrated that our in-house p38alpha MAPK is more potent (>30%) than a commercially available enzyme.

MeSH terms

  • Cloning, Molecular
  • Enzyme Activation
  • Escherichia coli / metabolism*
  • Humans
  • Kinetics
  • MAP Kinase Kinase 6 / biosynthesis
  • Mitogen-Activated Protein Kinase 14 / biosynthesis*
  • Mitogen-Activated Protein Kinase 14 / isolation & purification
  • Recombinant Proteins / biosynthesis
  • Solubility

Substances

  • Recombinant Proteins
  • Mitogen-Activated Protein Kinase 14
  • MAP Kinase Kinase 6
  • MAP2K6 protein, human