7ZPY

Influenza polymerase A C-terminal domain of PA subunit with optimized small peptide inhibitor

7ZPY の概要

• エントリーDOI: 10.2210/pdb7zpy/pdb
• 分子名称: Polymerase acidic protein, Peptide inhibitor (ASP-TYR-ASN-PRO-TYR-LEU-LEU-TYR-LEU-LYS), METHOXY-ETHOXYL, ... (4 entities in total)
• 機能のキーワード: antiviral peptides, influenza a polymerase, protein-protein interaction, viral protein
• 由来する生物種: Influenza A virus (A/California/07/2009(H1N1)); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 54317.22

構造登録者

Radilova, K.,Brynda, J. (登録日: 2022-04-29, 公開日: 2022-10-26, 最終更新日: 2024-01-31)

主引用文献

Radilova, K.,Zima, V.,Kral, M.,Machara, A.,Majer, P.,Hodek, J.,Weber, J.,Brynda, J.,Strmen, T.,Konvalinka, J.,Kozisek, M.
Thermodynamic and structural characterization of an optimized peptide-based inhibitor of the influenza polymerase PA-PB1 subunit interaction.
Antiviral Res., 208:105449-105449, 2022

PubMed Abstract: Influenza virus causes severe respiratory infection in humans. Current antivirotics target three key proteins in the viral life cycle: neuraminidase, the M2 channel and the endonuclease domain of RNA-dependent-RNA polymerase. Due to the development of novel pandemic strains, additional antiviral drugs targetting different viral proteins are still needed. The protein-protein interaction between polymerase subunits PA and PB1 is one such possible target. We recently identified a modified decapeptide derived from the N-terminus of the PB1 subunit with high affinity for the C-terminal part of the PA subunit. Here, we optimized its amino acid hotspots to maintain the inhibitory potency and greatly increase peptide solubility. This allowed thermodynamic characterization of peptide binding to PA. Solving the X-ray structure of the peptide-PA complex provided structural insights into the interaction. Additionally, we optimized intracellular delivery of the peptide using a bicyclic strategy that led to improved inhibition in cell-based assays.

PubMed: 36265804
DOI: 10.1016/j.antiviral.2022.105449

実験手法

X-RAY DIFFRACTION (1.9 Å)