In vivo phosphorylation of a peptide tag for protein purification

Biotechnol Lett. 2016 May;38(5):767-72. doi: 10.1007/s10529-016-2040-4. Epub 2016 Jan 12.

Abstract

Objectives: To design a new system for the in vivo phosphorylation of proteins in Escherichia coli using the co-expression of the α-subunit of casein kinase II (CKIIα) and a target protein, (Nanofitin) fused with a phosphorylatable tag.

Results: The level of the co-expressed CKIIα was controlled by the arabinose promoter and optimal phosphorylation was obtained with 2 % (w/v) arabinose as inductor. The effectiveness of the phosphorylation system was demonstrated by electrophoretic mobility shift assay (NUT-PAGE) and staining with a specific phosphoprotein-staining gel. The resulting phosphorylated tag was also used to purify the phosphoprotein by immobilized metal affinity chromatography, which relies on the specific interaction of phosphate moieties with Fe(III).

Conclusion: The use of a single tag for both the purification and protein array anchoring provides a simple and straightforward system for protein analysis.

Keywords: Casein kinase II; Nanofitin; Phosphorylated peptide tag; Phosphorylation; Protein purification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Casein Kinase II / genetics
  • Casein Kinase II / metabolism*
  • Electrophoretic Mobility Shift Assay
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Gene Expression
  • Phosphorylation
  • Protein Processing, Post-Translational*
  • Protein Subunits / genetics
  • Protein Subunits / metabolism
  • Proteins / isolation & purification*
  • Proteins / metabolism*
  • Recombinant Fusion Proteins / isolation & purification*
  • Recombinant Fusion Proteins / metabolism*

Substances

  • Protein Subunits
  • Proteins
  • Recombinant Fusion Proteins
  • Casein Kinase II