Reaction Mechanism of Histone Demethylation in αKG-dependent Non-Heme Iron Enzymes

J Phys Chem B. 2019 Sep 19;123(37):7801-7811. doi: 10.1021/acs.jpcb.9b06064. Epub 2019 Sep 10.

Abstract

Histone demethylases (KDMs) catalyze histone lysine demethylation, an important epigenetic process that controls gene expression in eukaryotes, and represent important cancer drug targets for cancer treatment. Demethylation of histone is comprised of sequential reaction steps including oxygen activation, decarboxylation, and demethylation. The initial oxygen binding and activation steps have been studied. However, the information on the complete catalytic reaction cycle is limited, which has impeded the structure-based design of inhibitors targeting KDMs. Here we report the mechanism of the complete reaction steps catalyzed by a representative nonheme iron αKG-dependent KDM, PHF8 using QM/MM approaches. The atomic-level understanding on the complete reaction mechanism of PHF8 would shed light on the structure-based design of selective inhibitors targeting KDMs to intervene in cancer epigenetics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biocatalysis
  • Demethylation
  • Enzyme Inhibitors / pharmacology
  • Histone Demethylases / antagonists & inhibitors
  • Histone Demethylases / chemistry
  • Histone Demethylases / metabolism*
  • Histones / chemistry
  • Histones / metabolism*
  • Humans
  • Oxygen / chemistry
  • Oxygen / metabolism
  • Quantum Theory
  • Transcription Factors / antagonists & inhibitors
  • Transcription Factors / chemistry
  • Transcription Factors / metabolism*

Substances

  • Enzyme Inhibitors
  • Histones
  • Transcription Factors
  • Histone Demethylases
  • PHF8 protein, human
  • Oxygen