Dupouy Baptiste, Cotos Leandro, Binder Annika, Slavikova Lucie, Rottmann Matthias, Mäser Pascal, Jacquemin Denis, Ganter Markus, Davioud-Charvet Elisabeth, Elhabiri Mourad
Laboratoire d'Innovation Moléculaire et Applications, UMR 7042, CNRS-Unistra-UHA, ECPM, 25 Rue Becquerel, 67200, Strasbourg, France.
Heidelberg University, Medical Faculty, Centre for Infectious Diseases, Im Neuenheimer Feld 324/344, 69120, Heidelberg, Germany.
Chemistry. 2025 Jan 27;31(6):e202403691. doi: 10.1002/chem.202403691. Epub 2024 Dec 16.
The development of redox-sensitive molecular fluorescent probes for the detection of redox changes in Plasmodium falciparum-parasitized red blood cells remains of interest due to the limitations of current genetically encoded biosensors. This study describes the design, screening and synthesis of new pro-fluorophores based on flavylium azido dyes coupled by CuAAC click chemistry to alkynyl analogues of plasmodione oxide, the key metabolite of the potent redox-active antimalarial plasmodione. The photophysical and electrochemical properties of these probes were evaluated, focusing on their fluorogenic responses. The influence of both the redox status of the quinone and the length of the PEG chain separating the fluorophore from the electrophore on the photophysical properties was investigated. The fluorescence quenching by photoinduced electron transfer is reversible and of high amplitude for probes in oxidized quinone forms and fluorescence is reinstated for reduced hydroquinone forms. Our results demonstrate that shortening the PEG chain has the effect of enhancing the fluorogenic response, likely due to non-covalent interactions between the two chromophores. All these systems were evaluated for their antiparasitic activities and fluorescence imaging suggests the efficacy of the fluorescent flavylium dyes in P. falciparum-parasitized red blood cells, paving the way for future parasite imaging studies to monitor cellular redox processes.
由于当前基因编码生物传感器存在局限性,开发用于检测恶性疟原虫寄生红细胞中氧化还原变化的氧化还原敏感分子荧光探针仍备受关注。本研究描述了基于黄酮叠氮染料的新型前体荧光团的设计、筛选和合成,这些染料通过铜催化的叠氮化物-炔烃环加成(CuAAC)点击化学与氧化疟原酮的炔基类似物偶联,氧化疟原酮是强效氧化还原活性抗疟药物疟原酮的关键代谢产物。评估了这些探针的光物理和电化学性质,重点关注它们的荧光生成响应。研究了醌的氧化还原状态以及将荧光团与电子受体分开的聚乙二醇(PEG)链长度对光物理性质的影响。对于氧化醌形式的探针,光致电子转移引起的荧光猝灭是可逆的且幅度很大,而对于还原的对苯二酚形式,荧光得以恢复。我们的结果表明,缩短PEG链具有增强荧光生成响应的作用,这可能是由于两个发色团之间的非共价相互作用。评估了所有这些体系的抗寄生虫活性,荧光成像表明荧光黄酮染料在恶性疟原虫寄生的红细胞中具有有效性,为未来监测细胞氧化还原过程的寄生虫成像研究铺平了道路。