化学
配体(生物化学)
反应性(心理学)
荧光
阳离子聚合
共焦显微镜
化学稳定性
X射线吸收光谱法
结晶学
立体化学
吸收光谱法
高分子化学
生物化学
有机化学
生物
受体
病理
物理
细胞生物学
替代医学
医学
量子力学
作者
Hester Blommaert,Clément Soep,Edwyn Remadna,Héloïse Dossmann,Murielle Salomé,Olivier Proux,Isabelle Kieffer,Jean‐Louis Hazemann,Sylvain Bohic,Michèle Salmain,Benoı̂t Bertrand
标识
DOI:10.1002/anie.202422763
摘要
We present a comprehensive study on the chemical reactivity in gas phase, with amino acids and peptides and in 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 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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