Structure–activity based study of the Smac-binding pocket within the BIR3 domain of XIAP

A small series of peptide mimics was designed and synthesized to contain a heterocyclic ring in place of the potentially labile N-terminal peptide bond of the tetrapeptide containing the Smac-XIAP-binding motif. Two Smac mimics were shown to bind to the BIR3 domain of XIAP with moderate affinity and one displayed increased activity in cells relative to the Smac peptides. The structures of BIR3-XIAP in complex with a Smac peptide and a peptide mimic were solved and analyzed to elucidate the structure–activity relationship surrounding the Smac-binding domain within BIR3-XIAP.

A small series of peptide mimics was designed and synthesized to contain a heterocyclic ring in place of the potentially labile N-terminal peptide bond of the tetrapeptide containing the Smac-XIAP-binding motif. The structure–activity relationship between the peptide mimics and XIAP was analyzed in detail. Image shows a surface representation of one peptide mimic, ‘AoxSPW’, bound to the BIR3 domain of XIAP.Figure optionsDownload as PowerPoint slide