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Key Intermediate Species Reveal the Copper(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...

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Detalles Bibliográficos
Autores principales: Kotuniak, Radosław, Strampraad, Marc J. F., Bossak‐Ahmad, Karolina, Wawrzyniak, Urszula E., Ufnalska, Iwona, Hagedoorn, Peter‐Leon, Bal, Wojciech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383912/
https://www.ncbi.nlm.nih.gov/pubmed/32267054
http://dx.doi.org/10.1002/anie.202004264
Descripción
Sumario: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)≈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.