Issue 24, 2022

Evidence for H-bonding interactions to the μ-η22-peroxide of oxy-tyrosinase that activate its coupled binuclear copper site

Abstract

The factors that control the diverse reactivity of the μ-η22-peroxo dicopper(II) oxy-intermediates in the coupled binuclear copper proteins remain elusive. Here, spectroscopic and computational methods reveal H-bonding interactions between active-site waters and the μ-η22-peroxide of oxy-tyrosinase, and define their effects on the Cu(II)2O2 electronic structure and O2 activation.

Graphical abstract: Evidence for H-bonding interactions to the μ-η2:η2-peroxide of oxy-tyrosinase that activate its coupled binuclear copper site

Supplementary files

Article information

Article type
Communication
Submitted
06 Feb 2022
Accepted
22 Feb 2022
First published
23 Feb 2022

Chem. Commun., 2022,58, 3913-3916

Evidence for H-bonding interactions to the μ-η22-peroxide of oxy-tyrosinase that activate its coupled binuclear copper site

I. Kipouros, A. Stańczak, M. Culka, E. Andris, T. R. Machonkin, L. Rulíšek and E. I. Solomon, Chem. Commun., 2022, 58, 3913 DOI: 10.1039/D2CC00750A

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