2026/01/01 by Kazuya Kobayashi, Yuki Yamaguchi, Mizuki Itahara +6 · 1 voice
Biochemistry, Genetics and Molecular Biology · Medicine · #Respiratory viral infections research #Virology and Viral Diseases #vaccines and immunoinformatics approaches
paper · doi:10.1039/d6md00211k
openalex publication_date 2026/01/01 · openalex created_date 2026/05/14 · openalex updated_date 2026/07/30
Although measles has been effectively controlled by vaccination, sporadic outbreaks still occur worldwide, highlighting the need for antiviral agents as complementary measures to achieve sustained elimination. Previously, we reported an anti-measles virus (MV) peptide derived from the HR2 region of MV fusion (F) protein that inhibits viral membrane fusion by disrupting the interaction between HR1 and HR2 regions. Here, we aimed to optimize this peptide by minimizing its sequence and interaction characteristics, thereby identifying a short derivative that retains potent antiviral activity. Structure-activity relationship analyses revealed that both hydrophobic and polar residues in HR2-derived peptides are crucial for efficient interaction with HR1. Thermal stability analysis of potential six-helical bundles using HR1-40, a 40-residue peptide of the HR1 region, showed no clear correlation with antiviral activity. To address this, we designed HR1Y, a C-terminally extended HR1 variant, which allowed a more accurate assessment of complex stability. Furthermore, molecular modeling of the HR2-derived peptide-HR1Y complex reproduced several experimental trends and provided structural insight into the HR1-HR2 interface. These findings clarify the structural determinants of fusion inhibitors against MV and support the rational optimization of HR2-derived antiviral peptides.