Journal article

Publication year: 2017

Pages: 104-117

Journal: Free Radical Biology and Medicine

Volume number: 104

DOI Link: https://doi.org/10.1016/j.freeradbiomed.2017.01.001

Publisher: Elsevier

Abstract: 

The malaria parasite Plasmodium falciparum is exposed to multiple sources of oxidative challenge during its complex life cycle in the Anopheles vector and its human host. In order to further elucidate redox-based parasite host cell interactions and mechanisms of drug action, we targeted the genetically encoded glutathione redox sensor roGFP2 coupled to human glutaredoxin 1 (roGFP2-hGrx1) as well as the ratiometric pH sensor pHluorin to the apicoplast and the mitochondrion of P. falciparum. Using live cell imaging, this allowed for the first time the determination of the pH values of the apicoplast (7.12±0.40) and mitochondrion (7.37±0.09) in the intraerythrocytic asexual stages of the parasite. Based on the roGFP2-hGrx1 signals, glutathione-dependent redox potentials of −267 mV and −328 mV, respectively, were obtained. Employing these novel tools, initial studies on the effects of redox-active agents and clinically employed antimalarial drugs were carried out on both organelles.

Harvard Citation style: Mohring, F., Rahbari, M., Zechmann, B., Rahlfs, S., Przyborski, J., Meyer, A., et al. (2017) Determination of glutathione redox potential and pH value in subcellular compartments of malaria parasites, Free Radical Biology and Medicine, 104, pp. 104-117. https://doi.org/10.1016/j.freeradbiomed.2017.01.001

APA Citation style: Mohring, F., Rahbari, M., Zechmann, B., Rahlfs, S., Przyborski, J., Meyer, A., & Becker, K. (2017). Determination of glutathione redox potential and pH value in subcellular compartments of malaria parasites. Free Radical Biology and Medicine. 104, 104-117. https://doi.org/10.1016/j.freeradbiomed.2017.01.001