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

Author:

Chu Wen-Ting1ORCID,Suo Zucai2ORCID,Wang Jin3ORCID

Affiliation:

1. State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences 1 , Changchun, Jilin 130022, China

2. Department of Biomedical Sciences, Florida State University College of Medicine 2 , Tallahassee, Florida 32306, USA

3. Department of Chemistry & Physics, State University of New York at Stony Brook 3 , Stony Brook, New York 11794, USA

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.

Funder

National Natural Science Foundation of China

Youth Innovation Promotion Association of the Chinese Academy of Sciences

Publisher

AIP Publishing

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