3JBM

Electron cryo-microscopy of a virus-like particle of orange-spotted grouper nervous necrosis virus

3JBM の概要

• エントリーDOI: 10.2210/pdb3jbm/pdb
• EMDBエントリー: 6453
• 分子名称: virus-like particle of orange-spotted grouper nervous necrosis virus (1 entity in total)
• 機能のキーワード: virus-like particle, orange-spotted grouper nervous necrosis virus, betanodavirus, virus
• 由来する生物種: Orange-spotted grouper nervous necrosis virus (orange-spotted grouper)
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 111308.16

構造登録者

Xie, J.,Li, K.,Gao, Y.,Huang, R.,Lai, Y.,Shi, Y.,Yang, S.,Zhu, G.,Zhang, Q.,He, J. (登録日: 2015-09-06, 公開日: 2016-10-19, 最終更新日: 2024-03-20)

主引用文献

Xie, J.,Li, K.,Gao, Y.,Huang, R.,Lai, Y.,Shi, Y.,Yang, S.,Zhu, G.,Zhang, Q.,He, J.
Structural analysis and insertion study reveal the ideal sites for surface displaying foreign peptides on a betanodavirus-like particle
Vet. Res., 47:16-16, 2016

PubMed Abstract: Betanodavirus infection causes fatal disease of viral nervous necrosis in many cultured marine and freshwater fish worldwide and the virus-like particles (VLP) are effective vaccines against betanodavirus. But vaccine and viral vector designs of betanodavirus VLP based on their structures remain lacking. Here, the three-dimensional structure of orange-spotted grouper nervous necrosis virus (OGNNV) VLP (RBS) at 3.9 Å reveals the organization of capsid proteins (CP). Based on the structural results, seven putative important sites were selected to genetically insert a 6× histidine (His)-tag for VLP formation screen, resulting in four His-tagged VLP (HV) at positions N-terminus, Ala220, Pro292 and C-terminus. The His-tags of N-terminal HV (NHV) were concealed inside virions while those of 220HV and C-terminal HV (CHV) were displayed at the outer surface. NHV, 220HV and CHV maintained the same cell entry ability as RBS in the Asian sea bass (SB) cell line, indicating that their similar surface structures can be recognized by the cellular entry receptor(s). For application of vaccine design, chromatography-purified CHV could provoke NNV-specific antibody responses as strong as those of RBS in a sea bass immunization assay. Furthermore, in carrying capacity assays, N-terminus and Ala220 can only carry short peptides and C-terminus can even accommodate large protein such as GFP to generate fluorescent VLP (CGV). For application of a viral vector, CGV could be real-time visualized to enter SB cells in invasion study. All the results confirmed that the C-terminus of CP is a suitable site to accommodate foreign peptides for vaccine design and viral vector development.

PubMed: 26754256
DOI: 10.1186/s13567-015-0294-9

実験手法

ELECTRON MICROSCOPY (3.9 Å)