Based on ESI-MS measurements, we show here that some representative cytotoxic gold(iii) compounds produce stable adducts upon reaction with the copper chaperone Atox-1; notably, such adducts contain gold in the oxidation state +1. These findings are of interest to understand the intracellular metabolism of medicinal gold species and to develop new potent inhibitors of the copper trafficking system.

Medicinal gold compounds form tight adducts with the copper chaperone Atox-1: Biological and pharmacological implications

Michelucci E;
2012

Abstract

Based on ESI-MS measurements, we show here that some representative cytotoxic gold(iii) compounds produce stable adducts upon reaction with the copper chaperone Atox-1; notably, such adducts contain gold in the oxidation state +1. These findings are of interest to understand the intracellular metabolism of medicinal gold species and to develop new potent inhibitors of the copper trafficking system.
2012
Inglese
48
95
11623
11625
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84869014485&doi=10.1039%2fc2cc36610j&partnerID=40&md5=2c9d5fd34c0baaf31c256329ee95f3e7
auranofin
chaperone; copper; gold derivative; protein Atox 1; unclassified drug
article; binding site; chemical reaction; complex formation; cytotoxicity; density functional theory; drug protein binding; drug stability; drug structure; electrospray mass spectrometry; oxidation
cited By 26
1
info:eu-repo/semantics/article
262
Gabbiani C;Scaletti F;Massai L;Michelucci E;Cinellu; M A;Messori; L
01 Contributo su Rivista::01.01 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/415831
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