Inhibition of the 26S proteasome as a possible mechanism for toxicity of heavy metal species.

Inhibition of the 26S proteasome as a possible mechanism for toxicity of heavy metal species.
J Inorg Biochem. 2014 Jan 8;
Authors: Tomco D, Schmitt S, Heeg MJ, Dou QP, Verani CN
Abstract
In this paper we report on the synthesis of five metal complexes coordinated to the [NN'O] ligand HL(iodo) (2,4-diiodo-6-((pyridine-2-ylmethylamino)methyl)phenol), namely [Al(III)(L(iodo))2]ClO4 (1), [Cd(II)(L(iodo))Cl]·H2O (2), [Hg(II)(L(iodo))2]·4DMSO (3), [Pb(II)(L(iodo))NO3] (4), and [Sn(IV)(L(iodo))Cl3] (5). Species 1-5 are thoroughly characterized by spectroscopic and spectrometric methods, as well as by elemental analysis. X-ray crystallography results for complex 3 indicate the presence of Hg(II) ion hexacoordinated to two facially oriented [NN'O] ligands, whereas for complex 5 an Sn(IV) ion chelates to one deprotonated ligand and three chlorido coligands. The toxicity of species 1-5 is tested against transformed human prostate epithelial cells CRL2221 and we observe that the five complexes demonstrate high levels of cell growth inhibition in a dose-dependent manner. In order to evaluate the relationship between these species and the proteasome, we test 1-5 against purified 20S, CRL2221 cell extracts, and intact cells, followed by the measurement of the percent chymotrypsin-like activity inhibition levels. Results suggest a good correlation between the toxicity of [Hg(II)(L(iodo))2]·4DMSO (3) and proteasome inhibition.
PMID: 24452142 [PubMe...

Source: Journal of Inorganic Biochemistry - January 8, 2014 Category: Biochemistry Authors: Tomco D, Schmitt S, Heeg MJ, Dou QP, Verani CN Tags: J Inorg Biochem Source Type: research