Protein-protein interactions (PPI) play crucial roles in various biological processes, which makes them attractive targets for therapeutic intervention. Despite growing interest in developing peptide mimetics as PPI inhibitors, a universal molecular framework remains elusive. Our research proposes the utilization of N-substituted peptides as a versatile framework for the design of self-standing peptide mimetics [1-5].
Oligo(N-methylalanine) (oligo-NMA) forms a distinctive extended shape in aqueous environments due to the pseudo-allylic strain per residue [1]. We employed oligo-NMA as a molecular scaffold to construct effective inhibitors of the MDM2-p53 interaction [1,3]. The MDM2-p53 interaction is mainly governed by three “hot spot” amino acid residues. By displaying these amino acids' side-chain structures on the oligo-NMA scaffold, we could design an inhibitor of the MDM2-p53 interaction rationally. Another advantage of the oligo-NMA scaffold is its high cell membrane permeability. Consequently, we also showed that the designed inhibitors function intracellularly [4]. Recently, we have demonstrated that by manipulating the L/D-chirality of alanine, the oligo-NMA, called heterochiral oligo-NMA, can adopt a wide array of structures beyond the aforementioned extended conformation [5]. Our research showcases the potential of oligo-NMA as a versatile platform for designing PPI inhibitors.
In this presentation, I will discuss the innovative use of oligo-NMA in developing PPI inhibitors. We are particularly excited to share the co-crystal structure of the oligo-NMA-based inhibitor with its target protein. This provides unprecedented insights into how the peptoid inhibitor interacts with the protein at the molecular level.
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