Issue 3, 2019

Organometallic ruthenium anticancer complexes inhibit human peroxiredoxin I activity by binding to and inducing oxidation of its catalytic cysteine residue

Abstract

Peroxiredoxins (Prxs) are a family of ubiquitous antioxidant proteins and the inhibition of Prxs would elevate the reactive oxygen species level so as to induce cancer cell death. The interactions of organometallic ruthenium arene anticancer complexes with proteins play important roles in their mechanisms of action. Herein, we demonstrate that Ru complexes [(η6-arene)Ru(en)Cl]+ (en = ethylenediamine, arene = p-cymene (1), biphenyl (2) and 9,10-dihydrophenanthrene (3)) can inhibit the enzymatic activity of human peroxiredoxin I (Prx-I) in an order of 1 > 3 > 2. Mass spectrometric (MS) analysis revealed that 1–3 coordinated to the catalytic site Cys173 of Prx-I, and partially induced the oxidation of the thiolate to sulfenate. Quantitative MS analysis demonstrated that the higher level of the ruthenation of Cys173 is correlated with the higher inhibitory potency of the Ru complexes against Prx-I, suggesting their binding to Cys173 accounts for their inhibition towards Prx-I.

Graphical abstract: Organometallic ruthenium anticancer complexes inhibit human peroxiredoxin I activity by binding to and inducing oxidation of its catalytic cysteine residue

Supplementary files

Article information

Article type
Paper
Submitted
06 dec 2018
Accepted
17 jan 2019
First published
17 jan 2019

Metallomics, 2019,11, 546-555

Spotlight

Advertisements