8AYY
Poliovirus type 3 (strain Saukett) stabilised virus-like particle (PV3 SC8) in complex with GSH and Pleconaril
8AYY の概要
| エントリーDOI | 10.2210/pdb8ayy/pdb |
| 関連するPDBエントリー | 8AYX 8AYZ |
| EMDBエントリー | 15725 15726 15727 |
| 分子名称 | Capsid protein, VP1, Capsid protein, VP0, Capsid protein, VP3, ... (5 entities in total) |
| 機能のキーワード | capsid protein, virus like particle, glutathione, inhibitor, complex |
| 由来する生物種 | Human poliovirus 3 詳細 |
| タンパク質・核酸の鎖数 | 3 |
| 化学式量合計 | 98189.58 |
| 構造登録者 | |
| 主引用文献 | Bahar, M.W.,Nasta, V.,Fox, H.,Sherry, L.,Grehan, K.,Porta, C.,Macadam, A.J.,Stonehouse, N.J.,Rowlands, D.J.,Fry, E.E.,Stuart, D.I. A conserved glutathione binding site in poliovirus is a target for antivirals and vaccine stabilisation. Commun Biol, 5:1293-1293, 2022 Cited by PubMed Abstract: Strategies to prevent the recurrence of poliovirus (PV) after eradication may utilise non-infectious, recombinant virus-like particle (VLP) vaccines. Despite clear advantages over inactivated or attenuated virus vaccines, instability of VLPs can compromise their immunogenicity. Glutathione (GSH), an important cellular reducing agent, is a crucial co-factor for the morphogenesis of enteroviruses, including PV. We report cryo-EM structures of GSH bound to PV serotype 3 VLPs showing that it can enhance particle stability. GSH binds the positively charged pocket at the interprotomer interface shown recently to bind GSH in enterovirus F3 and putative antiviral benzene sulphonamide compounds in other enteroviruses. We show, using high-resolution cryo-EM, the binding of a benzene sulphonamide compound with a PV serotype 2 VLP, consistent with antiviral activity through over-stabilizing the interprotomer pocket, preventing the capsid rearrangements necessary for viral infection. Collectively, these results suggest GSH or an analogous tight-binding antiviral offers the potential for stabilizing VLP vaccines. PubMed: 36434067DOI: 10.1038/s42003-022-04252-5 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (2.6 Å) |
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