Baculovirus-mediated high level expression of a mammalian DNA methyltransferase

Biochem Biophys Res Commun. 1994 Nov 15;204(3):1003-8. doi: 10.1006/bbrc.1994.2562.

Abstract

The murine C-5 cytosine DNA methyltransferase (MTase, E.C.2.1.1.37) containing a hexahistidine affinity leader peptide has been expressed at levels which are at least 50-fold higher than previously reported. The recombinant enzyme has activity levels similar to the wild-type enzyme. The recombinant polypeptide binds to and elutes from a nickel affinity resin (IMAC resin). No dramatic differences in post-translational modification between the wild-type and recombinant enzyme were observed. The recombinant system will be useful in performing site-directed mutagenesis and will facilitate enzymological and biological investigations of this enzyme.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Baculoviridae*
  • Blotting, Western
  • Cell Line
  • Chromatography, Affinity
  • DNA (Cytosine-5-)-Methyltransferases / biosynthesis*
  • DNA (Cytosine-5-)-Methyltransferases / isolation & purification
  • DNA (Cytosine-5-)-Methyltransferases / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Mice
  • Protein Processing, Post-Translational
  • Recombinant Proteins / biosynthesis*
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Spodoptera
  • Transfection / methods

Substances

  • Recombinant Proteins
  • DNA (Cytosine-5-)-Methyltransferases