Spectroscopic and computational studies of a bifunctional iron- and 2-oxoglutarate dependent enzyme, AsqJ

Methods Enzymol. 2024:704:199-232. doi: 10.1016/bs.mie.2024.05.023. Epub 2024 Jun 29.

Abstract

Iron and 2-oxoglutarate dependent (Fe/2OG) enzymes exhibit an exceedingly broad reaction repertoire. The most prevalent reactivity is hydroxylation, but many other reactivities have also been discovered in recent years, including halogenation, desaturation, epoxidation, endoperoxidation, epimerization, and cyclization. To fully explore the reaction mechanisms that support such a diverse reactivities in Fe/2OG enzyme, it is necessary to utilize a multi-faceted research methodology, consisting of molecular probe design and synthesis, in vitro enzyme assay development, enzyme kinetics, spectroscopy, protein crystallography, and theoretical calculations. By using such a multi-faceted research approach, we have explored reaction mechanisms of desaturation and epoxidation catalyzed by a bi-functional Fe/2OG enzyme, AsqJ. Herein, we describe the experimental protocols and computational workflows used in our studies.

Keywords: Desaturation; Epoxidation; Ferryl; Iron and 2-oxoglutarate dependent enzymes; Molecular dynamics; Mössbauer; Oxyferryl; Protein crystallography; Reaction mechanism; Transient kinetics.

MeSH terms

  • Crystallography, X-Ray / methods
  • Enzyme Assays / methods
  • Hydroxylation
  • Iron* / chemistry
  • Iron* / metabolism
  • Ketoglutaric Acids* / chemistry
  • Ketoglutaric Acids* / metabolism
  • Kinetics
  • Models, Molecular

Substances

  • Ketoglutaric Acids
  • Iron