A divalent metal ion-dependent N(1)-methyl transfer to G37-tRNA

Chem Biol. 2014 Oct 23;21(10):1351-1360. doi: 10.1016/j.chembiol.2014.07.023. Epub 2014 Sep 11.

Abstract

The catalytic mechanism of the majority of S-adenosyl methionine (AdoMet)-dependent methyl transferases requires no divalent metal ions. Here we report that methyl transfer from AdoMet to N(1) of G37-tRNA, catalyzed by the bacterial TrmD enzyme, is strongly dependent on divalent metal ions and that Mg(2+) is the most physiologically relevant. Kinetic isotope analysis, metal rescue, and spectroscopic measurements indicate that Mg(2+) is not involved in substrate binding, but in promoting methyl transfer. On the basis of the pH-activity profile indicating one proton transfer during the TrmD reaction, we propose a catalytic mechanism in which the role of Mg(2+) is to help to increase the nucleophilicity of N(1) of G37 and stabilize the negative developing charge on O(6) during attack on the methyl sulfonium of AdoMet. This work demonstrates how Mg(2+) contributes to the catalysis of AdoMet-dependent methyl transfer in one of the most crucial posttranscriptional modifications to tRNA.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biocatalysis
  • Escherichia coli / metabolism
  • Escherichia coli Proteins / metabolism
  • Hydrogen-Ion Concentration
  • Ions / chemistry
  • Kinetics
  • Magnesium / chemistry
  • Magnesium / metabolism
  • Metals / chemistry
  • Metals / metabolism*
  • RNA, Transfer / chemistry
  • RNA, Transfer / metabolism*
  • S-Adenosylmethionine / chemistry
  • S-Adenosylmethionine / metabolism
  • tRNA Methyltransferases / metabolism

Substances

  • Escherichia coli Proteins
  • Ions
  • Metals
  • S-Adenosylmethionine
  • RNA, Transfer
  • TrmD protein, E coli
  • tRNA Methyltransferases
  • Magnesium