Investigation of the binding mode of a novel cruzain inhibitor by docking, molecular dynamics, ab initio and MM/PBSA calculations.

Chagas disease remains a major health problem in South America, and throughout the world. The two drugs clinically available for its treatment have limited efficacy and cause serious adverse effects. Cruzain is an established therapeutic target of <italic>Trypanosoma cruzi</italic>, the protozoan that causes Chagas disease. Our group recently identified a competitive cruzain inhibitor (compound <bold>1</bold>) with an IC₅₀ = 15 µM that is also more synthetically accessible than the previously reported lead, compound <bold>2</bold>. Prior studies, however, did not propose a binding mode for compound <bold>1</bold>, hindering understanding of the structure-activity relationship and optimization. Here, the cruzain binding mode of compound <bold>1</bold> was investigated using docking, molecular dynamics (MD) simulations with ab initio derived parameters, ab initio calculations, and MM/PBSA. Two ligand protonation states and four binding poses were evaluated. A careful ligand parameterization method was employed to derive more physically meaningful parameters than those obtained by automated tools. The poses of unprotonated <bold>1</bold> were unstable in MD, showing large conformational changes and diffusing away from the binding site, whereas the protonated form showed higher stability and interaction with negatively charged residues Asp161 and Cys25. MM/PBSA also suggested that these two residues contribute favorably to binding of compound <bold>1</bold>. By combining results from MD, ab initio calculations, and MM/PBSA, a binding mode of <bold>1</bold> is proposed. The results also provide insights for further optimization of <bold>1</bold>, an interesting lead compound for the development of new cruzain inhibitors. [ABSTRACT FROM AUTHOR]