Functional coexpression of serine protein kinase SRPK1 and its substrate ASF/SF2 in Escherichia coli

Nucleic Acids Res. 2000 Mar 1;28(5):E14. doi: 10.1093/nar/28.5.e14.

Abstract

Mammalian proteins expressed in Escherichia coli are used in a variety of applications. A major drawback in producing eukaryotic proteins in E.coli is that the bacteria lack most eukaryotic post-translational modification systems, including serine/threonine protein kinase(s). Here we show that a eukaryotic protein can be phosphorylated in E.coli by simultaneous expression of a mammalian protein kinase and its substrate. We show that in bacteria expressing SRPK1, ASF/SF2 becomes phosphorylated to a degree resembling native ASF/SF2 present in interphase HeLa cell nuclei. The E.coli phosphorylated ASF/SF2 is functional in splicing and, contrary to the unphosphorylated protein, soluble under native conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cloning, Molecular
  • Escherichia coli
  • HeLa Cells
  • Humans
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / isolation & purification
  • Nuclear Proteins / metabolism
  • Phosphorylation
  • Protein Serine-Threonine Kinases / genetics*
  • Protein Serine-Threonine Kinases / metabolism
  • RNA Splicing*
  • RNA-Binding Proteins
  • Recombinant Proteins / genetics
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Serine-Arginine Splicing Factors
  • Solubility

Substances

  • Nuclear Proteins
  • RNA-Binding Proteins
  • Recombinant Proteins
  • Serine-Arginine Splicing Factors
  • SRPK1 protein, human
  • Protein Serine-Threonine Kinases