Intramolecular Interactions Enhance the Potency of Gallinamide A Analogues against Trypanosoma cruzi
journal contributionposted on 21.02.2022, 15:37 authored by Elany Barbosa Da Silva, Vandna Sharma, Lilian Hernandez-Alvarez, Arthur H. Tang, Alexander Stoye, Anthony J. O’Donoghue, William H. Gerwick, Richard J. Payne, James H. McKerrow, Larissa M. Podust
Gallinamide A, a metabolite of the marine cyanobacterium Schizothrix sp., selectively inhibits cathepsin L-like cysteine proteases. We evaluated the potency of gallinamide A and 23 synthetic analogues against intracellular Trypanosoma cruzi amastigotes and the cysteine protease, cruzain. We determined the co-crystal structures of cruzain with gallinamide A and two synthetic analogues at ∼2 Å. SAR data revealed that the N-terminal end of gallinamide A is loosely bound and weakly contributes in drug–target interactions. At the C-terminus, the intramolecular π–π stacking interactions between the aromatic substituents at P1′ and P1 restrict the bioactive conformation of the inhibitors, thus minimizing the entropic loss associated with target binding. Molecular dynamics simulations showed that in the absence of an aromatic group at P1, the substituent at P1′ interacts with tryptophan-184. The P1–P1′ interactions had no effect on anti-cruzain activity, whereas anti-T. cruzi potency increased by ∼fivefold, likely due to an increase in solubility/permeability of the analogues.
Read the peer-reviewed publication
sar data revealedintramolecular interactions enhanceentropic loss associated∼ 2 ålike cysteine proteasestwo synthetic analogues23 synthetic analoguestrypanosoma cruzi gallinamidecruzi potency increasedp1 ′ interacts∼ fivefoldp1 ′cysteine proteaseweakly contributesthus minimizingterminal endtarget bindingp1 restrictloosely boundlikely duecrystal structuresbioactive conformationaromatic substituentsaromatic group