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Bioorthogonal Catalytic Activation of Platinum and Ruthenium Anticancer Complexes by FAD and Flavoproteins.


ABSTRACT: Recent advances in bioorthogonal catalysis promise to deliver new chemical tools for performing chemoselective transformations in complex biological environments. Herein, we report how FAD (flavin adenine dinucleotide), FMN (flavin mononucleotide), and four flavoproteins act as unconventional photocatalysts capable of converting PtIV and RuII complexes into potentially toxic PtII or RuII -OH2 species. In the presence of electron donors and low doses of visible light, the flavoproteins mini singlet oxygen generator (miniSOG) and NADH oxidase (NOX) catalytically activate PtIV prodrugs with bioorthogonal selectivity. In the presence of NADH, NOX catalyzes PtIV activation in the dark as well, indicating for the first time that flavoenzymes may contribute to initiating the activity of PtIV chemotherapeutic agents.

SUBMITTER: Alonso-de Castro S 

PROVIDER: S-EPMC5887934 | biostudies-literature | 2018 Mar

REPOSITORIES: biostudies-literature

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Bioorthogonal Catalytic Activation of Platinum and Ruthenium Anticancer Complexes by FAD and Flavoproteins.

Alonso-de Castro Silvia S   Cortajarena Aitziber L AL   López-Gallego Fernando F   Salassa Luca L  

Angewandte Chemie (International ed. in English) 20180215 12


Recent advances in bioorthogonal catalysis promise to deliver new chemical tools for performing chemoselective transformations in complex biological environments. Herein, we report how FAD (flavin adenine dinucleotide), FMN (flavin mononucleotide), and four flavoproteins act as unconventional photocatalysts capable of converting Pt<sup>IV</sup> and Ru<sup>II</sup> complexes into potentially toxic Pt<sup>II</sup> or Ru<sup>II</sup> -OH<sub>2</sub> species. In the presence of electron donors and l  ...[more]

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