Department of Chemistry, University of Sheffield, Sheffield, S3 7HF, UK.
Department of Biomedical Science, University of Sheffield, Sheffield, S10 2TN, UK.
Chemistry. 2023 Jun 19;29(34):e202300617. doi: 10.1002/chem.202300617. Epub 2023 May 2.
The synthesis of a new heterodinuclear Re Ru metallointercalator containing Ru (dppz) and Re (dppn) moieties is reported. Cell-free studies reveal that the complex has similar photophysical properties to its homoleptic M(dppz) analogue and it also binds to DNA with a similar affinity. However, the newly reported complex has very different in-cell properties to its parent. In complete contrast to the homoleptic system, the Ru (dppz)/Re (dppn) complex is not intrinsically cytotoxic but displays appreciable phototoxic, despite both complexes displaying very similar quantum yields for singlet oxygen sensitization. Optical microscopy suggests that the reason for these contrasting biological effects is that whereas the homoleptic complex localises in the nuclei of cells, the Ru (dppz)/Re (dppn) complex preferentially accumulates in mitochondria. These observations illustrate how even small structural changes in metal based therapeutic leads can modulate their mechanism of action.
报道了一种新的异双核 Re-Ru 金属嵌入剂的合成,其中含有 Ru(dppz)和 Re(dppn)部分。无细胞研究表明,该配合物具有与其同系物 M(dppz)类似的光物理性质,并且也以相似的亲和力与 DNA 结合。然而,新报道的配合物与其母体在细胞内的性质有很大的不同。与同系物系统完全相反,Ru(dppz)/Re(dppn)配合物本身没有细胞毒性,但具有明显的光毒性,尽管这两个配合物对单重态氧敏化的量子产率非常相似。光学显微镜表明,这些对比生物效应的原因是,同系物配合物定位于细胞的核内,而 Ru(dppz)/Re(dppn)配合物优先积聚在线粒体中。这些观察结果说明了即使是金属治疗先导物的微小结构变化也可以调节它们的作用机制。