CIC biomaGUNE, Paseo de Miramón 182, Donostia, 20014, Spain.
Ikerbasque, Basque Foundation for Science, Bilbao, 48011, Spain.
Angew Chem Int Ed Engl. 2018 Mar 12;57(12):3143-3147. doi: 10.1002/anie.201800288. Epub 2018 Feb 15.
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 and Ru complexes into potentially toxic Pt or Ru -OH 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 Pt prodrugs with bioorthogonal selectivity. In the presence of NADH, NOX catalyzes Pt activation in the dark as well, indicating for the first time that flavoenzymes may contribute to initiating the activity of Pt chemotherapeutic agents.
近年来,生物正交催化领域的进展有望为在复杂的生物环境中进行化学选择性转化提供新的化学工具。在此,我们报告了 FAD(黄素腺嘌呤二核苷酸)、FMN(黄素单核苷酸)和四种黄素蛋白如何作为非传统的光催化剂,将 Pt 和 Ru 配合物转化为潜在有毒的 Pt 或 Ru -OH 物种。在电子供体和低剂量可见光的存在下,黄素蛋白类迷你单线态氧发生器(miniSOG)和 NADH 氧化酶(NOX)以生物正交选择性催化激活 Pt 前药。在 NADH 的存在下,NOX 也可以在黑暗中催化 Pt 的激活,这表明首次发现黄素酶可能有助于启动 Pt 化疗药物的活性。