9IGA

Beta-hairpin macrocyclic peptide in complex with STAT1

Summary for 9IGA

• Entry DOI: 10.2210/pdb9iga/pdb
• Descriptor: Isoform Alpha of Signal transducer and activator of transcription 1-alpha/beta, OPG024 protein, ORTHO-XYLENE (3 entities in total)
• Functional Keywords: stat1, 018, poxvirus, transcription
• Biological source: Homo sapiens (human); More
• Total number of polymer chains: 2
• Total formula weight: 66540.43

Authors

Pantelejevs, T. (deposition date: 2025-02-19, release date: 2026-02-18)

Primary citation

Bula, A.L.,Bobrovs, R.,Arsenyan, P.,Pantelejevs, T.
Consequences of Peptide Macrocyclization Revealed by Virus-Inspired beta-Hairpin Mimetics.
Acs Chem.Biol., 21:160-169, 2026

PubMed Abstract: Mimicry of protein secondary structure elements, such as α-helices and β-sheets, using conformationally constrained peptide macrocycles, can be utilized to disrupt native protein-protein and protein-nucleic acid interactions. Although α-helical stapled peptides have been extensively studied as pharmacological probes, the application of β-sheet and β-hairpin mimetics remains comparatively limited. Less is known about the structural and biophysical consequences of β-hairpin macrocyclization in the context of target binding. In this work, we use a poxvirus immune antagonist protein 018 as a template for the structure-based design of β-hairpin mimetic macrocyclic peptides targeting the STAT1 transcription factor. We demonstrate that successive orthogonal cyclizations have additive effects on the thermodynamic and kinetic properties of peptide binding, most notably slowing the dissociation from the target. We elucidate the structural and dynamic consequences of interstrand and head-to-tail cross-linking and propose a kinetic model explaining the gains in target residence. Finally, we highlight the pharmacological potential of these peptides by competitive inhibition of STAT1 binding to its cognate interferon receptor docking site. These data suggest that β-hairpin macrocyclization may represent a general strategy to extend target engagement, with implications for peptidic probe design.

PubMed: 41427528
DOI: 10.1021/acschembio.5c00834

Experimental method

X-RAY DIFFRACTION (2.8 Å)