Molecular biophysics and inhibition mechanism of influenza virus A M2 viroporin by adamantane-based drugs – Challenges in designing antiviral agents

Journal article

The influenza A matrix 2 (AM2) protein is a prototype viroporin that conducts protons through an array of water molecules and sidechains of ionizable amino acid residues, with His37 being the most important. Amantadine is a prototype AM2 channel blocker and inhibitor of influenza A AM2 wild type (serine-31) replication. Amantadine received approval for prophylaxis against the influenza virus A in 1966. However, the characterization of the mechanism of action of amantadine targeting AM2 came 50 years after its approval as an anti-influenza A drug. We present results from experimental biophysical methods and molecular dynamics simulations for the complexes of the AM2 WT and amantadine-resistant mutant channels (V27A, L26F, S31N) in complex with adamantane-based ligands. Additionally, we describe critical experimental evidence from biochemical/functional and molecular biology experiments. Previous debates on the mechanism of drug binding and inhibition were due to the different membrane mimetic environment, the excess of the drug, and the method used, rather than the accuracy of the experiments. The collective knowledge acquired can inspire research for the development of new antivirals against influenza viruses and provide experience on the application of molecular biophysics to other viroporins

Authors: Georgiou, K; Kolokouris, D; Kolocouris, A

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Elsevier
• Journal: Journal of Structural Biology: X
• Volume: 11
• Pages: 100122-100122
• Publication date: 2025-02-04
• DOI: 10.1016/j.yjsbx.2025.100122
• EISSN: 2590-1524
• ISSN: 2590-1524
• Language: English
• Keywords: Antiviral drug; Potentiator; Drug; Drug discovery; Amantadine; Lead compound; Amino acid residue; Biophysics; Viral matrix protein; Rimantadine; Adamantane; Mechanism (biology); Biology; Virology; Mechanism of action; In vitro; Pharmacology; Biochemistry; Virus; Chemistry; Peptide sequence; Influenza A virus