6SK6

Cryo-EM structure of rhinovirus-B5

6SK6 の概要

• エントリーDOI: 10.2210/pdb6sk6/pdb
• EMDBエントリー: 10221
• 分子名称: Rhinovirus B5 VP4, Rhinovirus B5 VP2, Rhinovirus B5 VP1, ... (4 entities in total)
• 機能のキーワード: rv-a89, hrv-b5, virus, capsid protein
• 由来する生物種: Human rhinovirus B5; 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 93215.45

構造登録者

Wald, J.,Goessweiner-Mohr, N.,Blaas, D.,Pasin, M. (登録日: 2019-08-14, 公開日: 2019-09-04, 最終更新日: 2024-05-22)

主引用文献

Wald, J.,Pasin, M.,Richter, M.,Walther, C.,Mathai, N.,Kirchmair, J.,Makarov, V.A.,Goessweiner-Mohr, N.,Marlovits, T.C.,Zanella, I.,Real-Hohn, A.,Verdaguer, N.,Blaas, D.,Schmidtke, M.
Cryo-EM structure of pleconaril-resistant rhinovirus-B5 complexed to the antiviral OBR-5-340 reveals unexpected binding site.
Proc.Natl.Acad.Sci.USA, 116:19109-19115, 2019

PubMed Abstract: Viral inhibitors, such as pleconaril and vapendavir, target conserved regions in the capsids of rhinoviruses (RVs) and enteroviruses (EVs) by binding to a hydrophobic pocket in viral capsid protein 1 (VP1). In resistant RVs and EVs, bulky residues in this pocket prevent their binding. However, recently developed pyrazolopyrimidines inhibit pleconaril-resistant RVs and EVs, and computational modeling has suggested that they also bind to the hydrophobic pocket in VP1. We studied the mechanism of inhibition of pleconaril-resistant RVs using RV-B5 (1 of the 7 naturally pleconaril-resistant rhinoviruses) and OBR-5-340, a bioavailable pyrazolopyrimidine with proven in vivo activity, and determined the 3D-structure of the protein-ligand complex to 3.6 Å with cryoelectron microscopy. Our data indicate that, similar to other capsid binders, OBR-5-340 induces thermostability and inhibits viral adsorption and uncoating. However, we found that OBR-5-340 attaches closer to the entrance of the pocket than most other capsid binders, whose viral complexes have been studied so far, showing only marginal overlaps of the attachment sites. Comparing the experimentally determined 3D structure with the control, RV-B5 incubated with solvent only and determined to 3.2 Å, revealed no gross conformational changes upon OBR-5-340 binding. The pocket of the naturally OBR-5-340-resistant RV-A89 likewise incubated with OBR-5-340 and solved to 2.9 Å was empty. Pyrazolopyrimidines have a rigid molecular scaffold and may thus be less affected by a loss of entropy upon binding. They interact with less-conserved regions than known capsid binders. Overall, pyrazolopyrimidines could be more suitable for the development of new, broadly active inhibitors.

PubMed: 31462495
DOI: 10.1073/pnas.1904732116

実験手法

ELECTRON MICROSCOPY (3.2 Å)