Three-metal ion mechanism of cross-linked and uncross-linked DNA polymerase β: A theoretical study

J Chem Phys. 2024 Apr 21;160(15):155101. doi: 10.1063/5.0200109.

Abstract

In our recent publication, we have proposed a revised base excision repair pathway in which DNA polymerase β (Polβ) catalyzes Schiff base formation prior to the gap-filling DNA synthesis followed by β-elimination. In addition, the polymerase activity of Polβ employs the "three-metal ion mechanism" instead of the long-standing "two-metal ion mechanism" to catalyze phosphodiester bond formation based on the fact derived from time-resolved x-ray crystallography that a third Mg2+ was captured in the polymerase active site after the chemical reaction was initiated. In this study, we develop the models of the uncross-linked and cross-linked Polβ complexes and investigate the "three-metal ion mechanism" vs the "two-metal ion mechanism" by using the quantum mechanics/molecular mechanics molecular dynamics simulations. Our results suggest that the presence of the third Mg2+ ion stabilizes the reaction-state structures, strengthens correct nucleotide binding, and accelerates phosphodiester bond formation. The improved understanding of Polβ's catalytic mechanism provides valuable insights into DNA replication and damage repair.

MeSH terms

  • Biocatalysis
  • Catalysis
  • DNA Polymerase beta*
  • DNA Replication
  • Magnesium
  • Molecular Dynamics Simulation

Substances

  • DNA Polymerase beta
  • Magnesium