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Identification of potent and selective mechanism-based inhibitors of the cysteine protease cruzain using solid-phase
Lily Huang1, Alice Lee, Jonathan A Ellman
1Department of Chemistry, University of California, Berkeley, California 94720, USA.
Abstract:
Targeted libraries of ketone-based cysteine protease inhibitors were synthesized and screened against cruzain, a cysteine protease implicated in Chagas' disease. A number of single digit nanomolar, low molecular weight inhibitors were identified and optimized for solubility and potency. Specifically, the best inhibitors identified have K(i) values of 0.9-10 nM and molecular weights between 499 and 609 Da. The most effective inhibitor was also found to be greater than 1000-fold selective for cruzain relative to cathepsin B and 100-fold selective for cruzain relative to cathepsin L.
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