Departamento de Química Orgânica e Inorgânica, Universidade Federal do Ceará, Campus do Pici s/n, Cx. Postal 12200, Fortaleza, CE, 60440-900, Brazil.
Laboratório Integrado de Biomoléculas, Departamento de Patologia e Medicina Legal, Universidade Federal do Ceará, Fortaleza, CE, 60430-270, Brazil.
J Biol Inorg Chem. 2020 May;25(3):419-428. doi: 10.1007/s00775-020-01772-5. Epub 2020 Mar 14.
The cis-Ru(bpy)(Met) complex, where Met = L-methionine and bpy = 2,2'-bipyridine, was prepared and fully characterized. This complex was subjected to blue and green light photolysis (453 and 505 nm, respectively) in aqueous solution, leading to the release of methionine and formation of the cis-[Ru(bpy)(HO)] ion. This latter photoproduct was shown to subsequently interact with DNA, while DNA photocleavage was noticed. In agreement with these reactivities, this compound exhibited an exciting antibacterial action, particularly against Gram-positive bacteria Staphylococcus aureus and Staphylococcus epidermidis, which was enhanced upon blue light irradiation. Altogether, these results showed that our strategy was successful in producing light-triggered DNA-binding agents with pharmacological potential and a likely blocking reagent for efficient peptide chemistry formation.
顺式-[Ru(bpy)(Met)]配合物(其中 Met= L-蛋氨酸,bpy=2,2'-联吡啶)被制备并进行了全面的表征。该配合物在水溶液中分别进行蓝光(453nm)和绿光(505nm)光解,导致蛋氨酸的释放和 cis-[Ru(bpy)(HO)]离子的形成。随后,该光产物被证明与 DNA 相互作用,并观察到 DNA 光裂解。与这些反应性一致,该化合物表现出令人兴奋的抗菌作用,特别是对革兰氏阳性菌金黄色葡萄球菌和表皮葡萄球菌,在蓝光照射下增强。总之,这些结果表明,我们的策略成功地生产出具有药理潜力的光触发 DNA 结合剂和一种可能的有效阻断试剂,用于高效肽化学形成。