High affinity Grb2-SH3 domain ligand incorporating Cβ-substituted prolines in a Sos-derived decapeptide

Peptide ligands that disrupt MAPK pathways are of great interest for a better understanding of these signalling cascades and represent therefore an attractive target to control cell degenerative processes. In that context, selective disruption of the upstream Grb2/Sos complex in the Ras/MAPK cascade has focused extensive work. The Sos PPII decapeptide, which interacts with the Grb2-SH3 domains, has been modified in various positions and the best inhibitors designed so far are either dimeric ligands or peptoid analogues of the VPPPVPPRRR sequence. We report the synthesis of new Grb2 ligands in which the key Val5 residue has been replaced by a cis Cβ-substituted proline. Both fluorescence and ITC assays have been employed to measure the affinity of these substituted peptides for a recombinant Grb2 protein. Whereas proline in position 5 completely abolished the binding potency, a cis Cβ-methyl-L-proline restored the affinity. Other cis Cβ-proline substituents led to a complete loss of binding potency. Combining the best modifications: a cis Cβ-methylproline 5, N-acetylation, C-carboxamide and dimerization yielded a 560-fold affinity enhancement compared to the wild-type VPPPVPPRRR sequence. This study shows that Cβ-substituted prolines may constitute a new alternative for PPII ligands, combining entropy and enthalpy beneficial effects.

Sos-derived decapeptides incorporating Cβ-substituted prolines were synthesized and evaluated for their ability to bind recombinant Grb2. Affinities were increased up to 560 times compared to the wild-type peptide.Figure optionsDownload as PowerPoint slide