Structure-based design of a SARS-CoV-2 Omicron-specific inhibitor

التفاصيل البيبلوغرافية
العنوان: Structure-based design of a SARS-CoV-2 Omicron-specific inhibitor
المؤلفون: Kailu Yang, Chuchu Wang, Alex J. B. Kreutzberger, K. Ian White, Richard A. Pfuetzner, Luis Esquivies, Tomas Kirchhausen, Axel T. Brunger
المصدر: Proceedings of the National Academy of Sciences. 120
بيانات النشر: Proceedings of the National Academy of Sciences, 2023.
سنة النشر: 2023
مصطلحات موضوعية: Multidisciplinary
الوصف: The Omicron variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) introduced a relatively large number of mutations, including three mutations in the highly conserved heptad repeat 1 (HR1) region of the spike glycoprotein (S) critical for its membrane fusion activity. We show that one of these mutations, N969K induces a substantial displacement in the structure of the heptad repeat 2 (HR2) backbone in the HR1HR2 postfusion bundle. Due to this mutation, fusion-entry peptide inhibitors based on the Wuhan strain sequence are less efficacious. Here, we report an Omicron-specific peptide inhibitor designed based on the structure of the Omicron HR1HR2 postfusion bundle. Specifically, we inserted an additional residue in HR2 near the Omicron HR1 K969 residue to better accommodate the N969K mutation and relieve the distortion in the structure of the HR1HR2 postfusion bundle it introduced. The designed inhibitor recovers the loss of inhibition activity of the original longHR2_42 peptide with the Wuhan strain sequence against the Omicron variant in both a cell–cell fusion assay and a vesicular stomatitis virus (VSV)-SARS-CoV-2 chimera infection assay, suggesting that a similar approach could be used to combat future variants. From a mechanistic perspective, our work suggests the interactions in the extended region of HR2 may mediate the initial landing of HR2 onto HR1 during the transition of the S protein from the prehairpin intermediate to the postfusion state.
تدمد: 1091-6490
0027-8424
DOI: 10.1073/pnas.2300360120
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::45c4883d159c4a7d1431cf4a96acb4e6
https://doi.org/10.1073/pnas.2300360120
Rights: OPEN
رقم الانضمام: edsair.doi...........45c4883d159c4a7d1431cf4a96acb4e6
قاعدة البيانات: OpenAIRE
الوصف
تدمد:10916490
00278424
DOI:10.1073/pnas.2300360120