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-Structure paper
| タイトル | Nanobody-Mediated Neutralization Reveals an Achilles Heel for Norovirus. |
|---|---|
| ジャーナル・号・ページ | J Virol, Vol. 94, Issue 13, Year 2020 |
| 掲載日 | 2020年6月16日 |
 著者 | Anna D Koromyslova / Jessica M Devant / Turgay Kilic / Charles D Sabin / Virginie Malak / Grant S Hansman /  |
| PubMed 要旨 | Human norovirus frequently causes outbreaks of acute gastroenteritis. Although discovered more than five decades ago, antiviral development has, until recently, been hampered by the lack of a ...Human norovirus frequently causes outbreaks of acute gastroenteritis. Although discovered more than five decades ago, antiviral development has, until recently, been hampered by the lack of a reliable human norovirus cell culture system. Nevertheless, a lot of pathogenesis studies were accomplished using murine norovirus (MNV), which can be grown routinely in cell culture. In this study, we analyzed a sizeable library of nanobodies that were raised against the murine norovirus virion with the main purpose of developing nanobody-based inhibitors. We discovered two types of neutralizing nanobodies and analyzed the inhibition mechanisms using X-ray crystallography, cryo-electron microscopy (cryo-EM), and cell culture techniques. The first type bound on the top region of the protruding (P) domain. Interestingly, this nanobody binding region closely overlapped the MNV receptor-binding site and collectively shared numerous P domain-binding residues. In addition, we showed that these nanobodies competed with the soluble receptor, and this action blocked virion attachment to cultured cells. The second type bound at a dimeric interface on the lower side of the P dimer. We discovered that these nanobodies disrupted a structural change in the capsid associated with binding cofactors (i.e., metal cations/bile acid). Indeed, we found that capsids underwent major conformational changes following addition of Mg or Ca Ultimately, these nanobodies directly obstructed a structural modification reserved for a postreceptor attachment stage. Altogether, our new data show that nanobody-based inhibition could occur by blocking functional and structural capsid properties. This research discovered and analyzed two different types of MNV-neutralizing nanobodies. The top-binding nanobodies sterically inhibited the receptor-binding site, whereas the dimeric-binding nanobodies interfered with a structural modification associated with cofactor binding. Moreover, we found that the capsid contained a number of vulnerable regions that were essential for viral replication. In fact, the capsid appeared to be organized in a state of flux, which could be important for cofactor/receptor-binding functions. Blocking these capsid-binding events with nanobodies directly inhibited essential capsid functions. Moreover, a number of MNV-specific nanobody binding epitopes were comparable to human norovirus-specific nanobody inhibitors. Therefore, this additional structural and inhibition information could be further exploited in the development of human norovirus antivirals. |
 リンク | J Virol / PubMed:32321816 / PubMed Central |
| 手法 | EM (単粒子) / X線回折 |
| 解像度 | 1.72 - 4.7 Å |
| 構造データ |  EMDB-10596:  EMDB-10597:  EMDB-10598:  EMDB-10599:  EMDB-10600:  PDB-6xw4:  PDB-6xw5:  PDB-6xw6:  PDB-6xw7: |
| 化合物 |  ChemComp-EDO:  ChemComp-HOH:  ChemComp-TRS:  ChemComp-MG:  ChemComp-CHO: |
| 由来 |
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 キーワード |  VIRAL PROTEIN (ウイルスタンパク質) / MNV / neutralizing nanobody / VHH / norovirus (ノロウイルス) |
