Structure-based drug design, synthesis and biological assays of <italic>P. falciparum</italic> Atg3–Atg8 protein–protein interaction inhibitors.

Villa, Stefania; Legnani, Laura; Colombo, Diego; Gelain, Arianna; Lammi, Carmen; Bongiorno, Daniele; Ilboudo, Denise P.; McGee, Kellen E.; Bosch, Jürgen; Grazioso, Giovanni

The proteins involved in the autophagy (Atg) pathway have recently been considered promising targets for the development of new antimalarial drugs. In particular, inhibitors of the protein–protein interaction (PPI) between Atg3 and Atg8 of Plasmodium falciparum retarded the blood- and liver-stages of parasite growth. In this paper, we used computational techniques to design a new class of peptidomimetics mimicking the Atg3 interaction motif, which were then synthesized by click-chemistry. Surface plasmon resonance has been employed to measure the ability of these compounds to inhibit the Atg3–Atg8 reciprocal protein–protein interaction. Moreover, P. falciparum growth inhibition in red blood cell cultures was evaluated as well as the cyto-toxicity of the compounds.

DRUG design; PROTEIN-protein interactions; ANTIMALARIALS; AUTOPHAGY; PEPTIDOMIMETICS

Journal of Computer-Aided Molecular Design, 2018, Vol 32, Issue 3, p473

0920-654X

Academic Journal

10.1007/s10822-018-0102-5