Key intermediate species reveal the Cu(II) exchange pathway in biorelevant ATCUN/NTS complexes.

The amino-terminal copper and nickel/N-terminal site (ATCUN/NTS) present in proteins and bioactive peptides exhibits high affinity towards Cu II ions and have been implicated in human copper physiology. Little is known, however, about the rate and exact mechanism of formation of such complexes. We used the stopped-flow and microsecond freeze-hyperquenching (MHQ) techniques supported by steady-state spectroscopic and electrochemical data to demonstrate the formation of partially coordinated intermediate Cu II complexes formed by glycyl-glycyl-histidine (GGH) peptide, the simplest ATCUN/NTS model. One of these novel intermediates, characterized by two-nitrogen coordination, t (1/2) approximately 100 ms at pH = 6.0 and the ability to maintain the Cu II /Cu I redox pair is the best candidate for the long-sought reactive species in extracellular copper transport.