Melis Diana R, Hsiao Chiao-Yu, Combrinck Jill M, Wiesner Lubbe, Smith Gregory S
Department of Chemistry, University of Cape Town, PD Hahn, Chemistry Mall, Rondebosch, 7701, Cape Town, South Africa.
Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, Observatory, 7925, Cape Town, South Africa.
Chembiochem. 2021 May 4;22(9):1568-1572. doi: 10.1002/cbic.202000847. Epub 2021 Feb 4.
A fluorescent analogue of a previously synthesised N,N-chelated Ir complex was prepared by coordination of the organic ligand to an extrinsic bis(2-phenylpyridine)iridium(III) fluorophore. This cyclometallated Ir complex in itself displays good, micromolar activity against the chloroquine-sensitive NF54 strain of Plasmodium falciparum. Live-cell confocal microscopy found negligible localisation of the fluorescent complex within the digestive vacuole of the parasite. This eliminated the haem detoxification pathway as a potential mechanism of action. Similarly, no localisation of the complex within the parasitic nucleus was found, thus suggesting that this complex probably does not interfere with the DNA replication process. A substantial saturation of fluorescence from the complex was found near phospholipid structures such as the plasma and nuclear membranes but not in neutral lipid bodies. This indicates that an association with these membranes, or organelles such as the endoplasmic reticulum or branched mitochondrion, could be essential to the efficacies of these types of antimalarial compounds.
通过将有机配体与外在的双(2-苯基吡啶)铱(III)荧光团配位,制备了先前合成的N,N-螯合铱配合物的荧光类似物。这种环金属化铱配合物本身对氯喹敏感的恶性疟原虫NF54菌株显示出良好的微摩尔活性。活细胞共聚焦显微镜检查发现荧光复合物在寄生虫消化泡内的定位可忽略不计。这排除了血红素解毒途径作为潜在的作用机制。同样,未发现复合物在寄生细胞核内的定位,因此表明该复合物可能不会干扰DNA复制过程。在磷脂结构(如质膜和核膜)附近发现复合物荧光大量饱和,但在中性脂质体中未发现。这表明与这些膜或细胞器(如内质网或分支线粒体)的结合可能对这些类型抗疟化合物的疗效至关重要。