State of the Surface of Antibacterial Copper in Phosphate Buffered Saline

The state was investigated of the copper surface in phosphate buffered saline (PBS; 140 mM Cl-, 10 mM phosphate; pH 7) by a combination of cyclic voltammetry (CV) and chronoamperometry (CA) with in situ spectroscopic ellipsometry and Raman spectroscopy. After polarization, samples were analyzed ex situ. In agreement with expectations on the basis of the Pourbaix diagram, Cu2O and Cu4O3 were observed when polarizing the system above approximate to-0.05 V vs. Ag vertical bar AgCl vertical bar 3M KCl. The formation of Cu2O did not lead to a passivation of the system. Rather, the system dissolved under formation of soluble square planar CuCl42-, identified by its strong Raman peak approximate to 300 cm(-1). During dissolution, spectroscopic ellipsometry showed a film with a stable steady state thickness. Energy electron loss spectroscopy (EELS) analysis of a cross section of the oxide after removal from the electrolyte showed that the oxide was Cu2O. It is suggested that Cl-replaces oxygen vacancies in the oxide layer. As soon as oxidation to Cu-II becomes dominant, the dissolution proceeds to soluble CuII species. The outer surface of copper under these conditions is hence a Cu2O-like surface, with CuII complexes present in solution. (C) The Author(s) 2017. Published by ECS. All rights reserved

State of the Surface of Antibacterial Copper in Phosphate Buffered Saline

The state was investigated of the copper surface in phosphate buffered saline (PBS; 140 mM Cl-, 10 mM phosphate; pH 7) by a combination of cyclic voltammetry (CV) and chronoamperometry (CA) with in situ spectroscopic ellipsometry and Raman spectroscopy. After polarization, samples were analyzed ex situ. In agreement with expectations on the basis of the Pourbaix diagram, Cu2O and Cu4O3 were observed when polarizing the system above approximate to-0.05 V vs. Ag vertical bar AgCl vertical bar 3M KCl. The formation of Cu2O did not lead to a passivation of the system. Rather, the system dissolved under formation of soluble square planar CuCl42-, identified by its strong Raman peak approximate to 300 cm(-1). During dissolution, spectroscopic ellipsometry showed a film with a stable steady state thickness. Energy electron loss spectroscopy (EELS) analysis of a cross section of the oxide after removal from the electrolyte showed that the oxide was Cu2O. It is suggested that Cl-replaces oxygen vacancies in the oxide layer. As soon as oxidation to Cu-II becomes dominant, the dissolution proceeds to soluble CuII species. The outer surface of copper under these conditions is hence a Cu2O-like surface, with CuII complexes present in solution. (C) The Author(s) 2017. Published by ECS. All rights reserved

Deubiquitinase inhibition by WP1130 leads to ULK1 aggregation and blockade of autophagy

<p>Autophagy represents an intracellular degradation process which is involved in both regular cell homeostasis and disease settings. In recent years, the molecular machinery governing this process has been elucidated. The ULK1 kinase complex consisting of the serine/threonine protein kinase ULK1 and the adapter proteins ATG13, RB1CC1, and ATG101, is centrally involved in the regulation of autophagy initiation. This complex is in turn regulated by the activity of different nutrient- or energy-sensing kinases, including MTOR, AMPK, and AKT. However, next to phosphorylation processes it has been suggested that ubiquitination of ULK1 positively influences ULK1 function. Here we report that the inhibition of deubiquitinases by the compound WP1130 leads to increased ULK1 ubiquitination, the transfer of ULK1 to aggresomes, and the inhibition of ULK1 activity. Additionally, WP1130 can block the autophagic flux. Thus, treatment with WP1130 might represent an efficient tool to inhibit the autophagy-initiating ULK1 complex and autophagy.</p