Structure-based drug design studies of the interactions ofent-kaurane diterpenes derived from Wedelia paludosa with the Plasmodium falciparumsarco/endoplasmic reticulum Ca2+-ATPase PfATP6

• Published in: Memórias do Instituto Oswaldo Cruz 2015-04, Vol.110 (2), p.255-258
• Main Authors: Guimarães, Daniel Silqueira Martins, Fonseca, Amanda Luisa da, Batista, Ronan, Comar Junior, Moacyr, Oliveira, Alaíde Braga de, Taranto, Alex Gutterres, Varotti, Fernando de Pilla
• Format: Article
• Language: English
• Subjects: PARASITOLOGY; TROPICAL MEDICINE
• ISSN: 0074-0276; 1678-8060; 0074-0276
• DOI: 10.1590/0074-02760140415

Malaria is responsible for more deaths around the world than any other parasitic disease. Due to the emergence of strains that are resistant to the current chemotherapeutic antimalarial arsenal, the search for new antimalarial drugs remains urgent though hampered by a lack of knowledge regarding the molecular mechanisms of artemisinin resistance. Semisynthetic compounds derived from diterpenes from the medicinal plant Wedelia paludosawere tested in silico against the Plasmodium falciparumCa2+-ATPase, PfATP6. This protein was constructed by comparative modelling using the three-dimensional structure of a homologous protein, 1IWO, as a scaffold. Compound 21 showed the best docking scores, indicating a better interaction with PfATP6 than that of thapsigargin, the natural inhibitor. Inhibition of PfATP6 by diterpene compounds could promote a change in calcium homeostasis, leading to parasite death. These data suggest PfATP6 as a potential target for the antimalarial ent-kaurane diterpenes.