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Chemical Exchange at the Trinuclear Copper Center of Small Laccase from Streptomyces coelicolor

The trinuclear copper center (TNC) of laccase reduces oxygen to water with very little overpotential. The arrangement of the coppers and ligands in the TNC is known to be from many crystal structures, yet information about possible dynamics of the ligands is absent. Here, we report dynamics at the T...

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Detalles Bibliográficos
Autores principales: Dasgupta, Rubin, Gupta, Karthick B.S.S., Nami, Faezeh, de Groot, Huub J.M., Canters, Gerard W., Groenen, Edgar J.J., Ubbink, Marcellus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7335907/
https://www.ncbi.nlm.nih.gov/pubmed/32531206
http://dx.doi.org/10.1016/j.bpj.2020.05.022
Descripción
Sumario:The trinuclear copper center (TNC) of laccase reduces oxygen to water with very little overpotential. The arrangement of the coppers and ligands in the TNC is known to be from many crystal structures, yet information about possible dynamics of the ligands is absent. Here, we report dynamics at the TNC of small laccase from Streptomyces coelicolor using paramagnetic NMR and electron paramagnetic resonance spectroscopy. Fermi contact-shifted resonances tentatively assigned to histidine Hδ1 display a two-state chemical exchange with exchange rates in the order of 100 s(−1). In the electron paramagnetic resonance spectra, at least two forms are observed with different g(z)-values. It is proposed that the exchange processes reflect the rotational motion of histidine imidazole rings that coordinate the coppers in the TNC.