Aryl amide substituted fatty acids uncouple mitochondria in cancer cells, indicating potential for targeted therapy.
Aryl amide substituted fatty acids facilitate transmembrane proton transport and uncouple mitochondrial oxidative phosphorylation in cells, leading to cell death. Photocaging is a potential strategy to enable light-controlled activation of mitochondrial uncouplers with spatio-temporal control. In this work, aryl amide substituted fatty acid protonophores were photocaged with ortho-nitrobenzyl and 4,5-dimethoxy-2-nitrobenzyl groups. The caged protonophores could be activated by irradiation with UV light, demonstrated in vesicular transport assays and in vitro against MDA-MB-231 breast cancer cells.
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Rajasekar et al. (2025) studied this question.
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