Conversion of DNA methyltransferases into azidonucleosidyl transferases via synthetic cofactors

Nucleic Acids Res. 2005 Mar 18;33(5):1644-52. doi: 10.1093/nar/gki306. Print 2005.

Abstract

Aziridine-based cofactor mimics have been synthesized and are shown to undergo methyltransferase-dependent DNA alkylation. Notably, each cofactor mimic possesses an azide functionality, to which can be attached an assortment of unnatural groups following methyltransferase-dependent DNA delivery. DNA duplexes modified with these cofactor mimics are capable of undergoing the Staudinger ligation with phosphines tethered to biological functionalities following enzymatic modification. This methodology provides a new tool by which to selectively modify DNA in a methyltransferase-dependent way. The conversion of biological methyltransferases into azidonucleosidyl transferases demonstrated here also holds tremendous promise as a means of identifying, as yet, unknown substrates of methylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Azides / chemistry*
  • Aziridines / chemistry*
  • Biotinylation
  • Coenzymes / chemistry*
  • DNA / chemistry
  • DNA / metabolism*
  • Molecular Mimicry
  • Nucleosides / chemical synthesis
  • Nucleosides / chemistry
  • Nucleosides / metabolism*
  • Oligonucleotides / chemistry
  • Oligonucleotides / metabolism
  • Pentosyltransferases / metabolism*
  • Site-Specific DNA-Methyltransferase (Adenine-Specific) / metabolism*

Substances

  • Azides
  • Aziridines
  • Coenzymes
  • Nucleosides
  • Oligonucleotides
  • DNA
  • DNA modification methylase EcoRI
  • DNA modification methylase TaqI
  • Site-Specific DNA-Methyltransferase (Adenine-Specific)
  • Pentosyltransferases