A Chemically Programmed Proximal Ligand Enhances the Catalytic Properties of a Heme Enzyme

Research output: Research - peer-reviewArticle

  • Authors:
  • Anthony Green
  • Takahiro Hayashi
  • Peer R. E. Mittl
  • Donald Hilvert


Enzymes rely on complex interactions between precisely positioned active site residues as a mechanism to compensate for the limited functionality contained within the genetic code. Heme enzymes provide a striking example of this complexity, whereby the electronic properties of reactive ferryl intermediates are finely tuned through hydrogen bonding interactions between proximal ligands and neighboring amino acids. Here, we show that introduction of a chemically programmed proximal Nδ-methylhistidine (NMH) ligand into an engineered ascorbate peroxidase (APX2) overcomes the reliance on the conserved Asp-His hydrogen bonding interaction, leading to a catalytically modified enzyme (APX2 NMH) which is able to achieve a significantly higher
number of turnovers compared with APX2 without compromising catalytic efficiency. Structural, spectroscopic and kinetic characterization
of APX2 NMH and several active site variants reveals significant insights into the role of the Asp-His-Fe triad of heme peroxidases. More significantly, simplification of catalytic mechanisms through the incorporation of chemically optimized ligands may facilitate efforts to create and evolve new active site heme environments within proteins.

Bibliographical metadata

Original languageEnglish
Pages (from-to)11344-11352
Number of pages9
JournalJournal of the American Chemical Society
Issue number35
Early online date8 Aug 2016
StatePublished - 2016