8GQV
The Crystal Structures of a Swine SLA-2*HB01 Molecules Complexed with a CTL epitope from Asia1 serotype of Foot-and-mouth disease virus
8GQV の概要
| エントリーDOI | 10.2210/pdb8gqv/pdb |
| 分子名称 | MHC class I antigen, beta 2 microglobulin, As64, ... (4 entities in total) |
| 機能のキーワード | sla-2; foot-and-mouth disease virus; crystal; peptide; epitope; ctl; complex; peptide presentation; universal vaccine candidate, immune system, immune system-epitope complex, immune system/epitope |
| 由来する生物種 | Sus scrofa (pig) 詳細 |
| タンパク質・核酸の鎖数 | 6 |
| 化学式量合計 | 88472.29 |
| 構造登録者 | |
| 主引用文献 | Feng, L.,Gao, Y.Y.,Sun, M.,Li, Z.B.,Zhang, Q.,Yang, J.,Qiao, C.,Jin, H.,Feng, H.S.,Xian, Y.H.,Qi, J.,Gao, G.F.,Liu, W.J.,Gao, F.S. The Parallel Presentation of Two Functional CTL Epitopes Derived from the O and Asia 1 Serotypes of Foot-and-Mouth Disease Virus and Swine SLA-2*HB01: Implications for Universal Vaccine Development. Cells, 11:-, 2022 Cited by PubMed Abstract: Foot-and-mouth disease virus (FMDV) poses a significant threat to the livestock industry. Through their recognition of the conserved epitopes presented by the swine leukocyte antigen (SLA), T cells play a pivotal role in the antiviral immunity of pigs. Herein, based on the peptide binding motif of SLA-2*HB01, from an original SLA-2 allele, a series of functional T-cell epitopes derived from the dominant antigen VP1 of FMDV with high binding capacity to SLA-2 were identified. Two parallel peptides, Hu64 and As64, from the O and Asia I serotypes, respectively, were both crystallized with SLA-2*HB01. Compared to SLA-1 and SLA-3, the SLA-2 structures showed the flexibility of residues in the P4, P6, and P8 positions and in their potential interface with TCR. Notably, the peptides Hu64 and As64 adopted quite similar overall conformation when bound to SLA-2*HB01. Hu64 has two different conformations, a more stable 'chair' conformation and an unstable 'boat' conformation observed in the two molecules of one asymmetric unit, whereas only a single 'chair' conformation was observed for As64. Both Hu64 and As64 could induce similar dominant T-cell activities. Our interdisciplinary study establishes a basis for the in-depth interpretation of the peptide presentation of SLA-I, which can be used toward the development of universal vaccines. PubMed: 36552780DOI: 10.3390/cells11244017 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.4 Å) |
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