Peptide stapling by late-stage Suzuki–Miyaura cross-coupling

Abstract

The development of peptide stapling techniques to stabilise α-helical secondary structure motifs of peptides led to the design of modulators of protein–protein interactions, which had been considered undruggable for a long time. We disclose a novel approach towards peptide stapling utilising macrocyclisation by late-stage Suzuki–Miyaura cross-coupling of bromotryptophan-containing peptides of the catenin-binding domain of axin. Optimisation of the linker length in order to find a compromise between both sufficient linker rigidity and flexibility resulted in a peptide with an increased α-helicity and enhanced binding affinity to its native binding partner β-catenin. An increased proteolytic stability against proteinase K has been demonstrated.

Keywords

• accelerated molecular dynamics
• halotryptophan
• intrinsically disordered peptides
• late-stage diversification
• macrocyclisation
• molecular dynamics
• stapled peptides
• suzuki–miyaura cross-coupling