Stability and Mitochondrial Localization of a Highly Cytotoxic Organogold(III) Complex with Diphosphine Ancillary Ligand in Lung Cancer Cells

Abstract We present a comprehensive study on the chemical reactivity in the gas phase, with amino acids and peptides, and in the cell, the anticancer activity and localization of a series of seven cationic biphenyl gold(III) complexes with aryl, alkyl, and chiral diphosphine ancillary ligands. Despite some structural differences, all the complexes similarly featured high stability toward reduction or ligand exchange in cell‐free conditions. The biphenyl Au(III) complex including the 1,2‐diphenylphosphinoethane (dppe) ligand manifested the same high stability in a cellular setting, as attested by a combination of cryo‐Synchrotron Radiation‐X‐Ray Fluorescence (cryo‐SR‐XRF) nano‐imaging and cryo‐Synchrotron Radiation‐X‐ray Absorption Spectroscopy (cryo‐SR‐XAS) measurements. Tandem cryo‐SR‐XRF elemental mapping and confocal fluorescence microscopy demonstrated the selective accumulation of the dppe complex in mitochondria. This represents the first study of the speciation and distribution of an organogold(III) complex in cancer cells.

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Publication Details

Journal
Angewandte Chemie
Published
2025-03-14
DOI
https://doi.org/10.1002/ange.202422763
Primary Topic
Metal complexes synthesis and properties
Type
article
Field-Weighted Citation Impact
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article

Stability and Mitochondrial Localization of a Highly Cytotoxic Organogold(III) Complex with Diphosphine Ancillary Ligand in Lung Cancer Cells

Benoı̂t Bertrand, Edwyn Remadna, Sylvain Bohic, Héloïse Dossmann et al.
Angewandte Chemie
Metal complexes synthesis and properties
article

Stability and Mitochondrial Localization of a Highly Cytotoxic Organogold(III) Complex with Diphosphine Ancillary Ligand in Lung Cancer Cells

Benoı̂t Bertrand, Edwyn Remadna, Sylvain Bohic, Héloïse Dossmann, Jean‐Louis Hazemann, Michèle Salmain, Olivier Proux, Hester Blommaert, Clément Soep, Isabelle Kieffer, Murielle Salomé
article en

Abstract

Abstract We present a comprehensive study on the chemical reactivity in the gas phase, with amino acids and peptides, and in the cell, the anticancer activity and localization of a series of seven cationic biphenyl gold(III) complexes with aryl, alkyl, and chiral diphosphine ancillary ligands. Despite some structural differences, all the complexes similarly featured high stability toward reduction or ligand exchange in cell‐free conditions. The biphenyl Au(III) complex including the 1,2‐diphenylphosphinoethane (dppe) ligand manifested the same high stability in a cellular setting, as attested by a combination of cryo‐Synchrotron Radiation‐X‐Ray Fluorescence (cryo‐SR‐XRF) nano‐imaging and cryo‐Synchrotron Radiation‐X‐ray Absorption Spectroscopy (cryo‐SR‐XAS) measurements. Tandem cryo‐SR‐XRF elemental mapping and confocal fluorescence microscopy demonstrated the selective accumulation of the dppe complex in mitochondria. This represents the first study of the speciation and distribution of an organogold(III) complex in cancer cells.

Angewandte ChemieVol. 137(22)
Centre National de la Recherche Scientifique (FR), Inserm (FR), European Synchrotron Radiation Facility (FR), Sorbonne Université (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), Laboratoire Interdisciplinaire de Physique (FR), Institut Néel (FR), Unité d'Appui et de Recherche OSUPS (FR), Institut Parisien de Chimie Moléculaire (FR), Institut de Recherche pour le Développement (FR), Synchrotron Radiation for Biomedicine, Université Grenoble Alpes (FR)
Openalex Percentile: Top 93%
Metal complexes synthesis and properties
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