When the strategies for cellular selectivity fail. Challenges and surprises in the design and application of fluorescent benzothiadiazole derivatives for mitochondrial staining
Literature Information
Jose R. Correa, Karen L. R. Paiva, Michele Baril, Daniel F. S. Machado, Jackson D. Scholten, Paulo E. N. de Souza, Fabiane H. Veiga-Souza, John Spencer
This work describes a series of fluorescent 2,1,3-benzothiadiazole derivatives (neutral, singly-charged and doubly-charged) to act as bioprobes for mitochondria. The results showed the flaws in the molecular architecture of this class of fluorophores and our attempts to direct the synthesized derivatives to the organelle. Unexpected results also showed a need for new strategies to predict the cellular selectivity of these derivatives. One of the singly-charged derivatives could stain mitochondria selectively whereas the doubly-charged stained the plasma membrane in an unexpected but highly selective manner. Co-staining experiments confirmed the cellular localization of the new derivatives. EPR experiments demonstrated the fluorescent marker that is selective for mitochondria does not interfere in the ROS production of the cells.
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Organic Chemistry Frontiers

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry














