8ULF
Crystal structure of Plasmodium vivax CelTOS in complex with antibody 7g7
8ULF の概要
| エントリーDOI | 10.2210/pdb8ulf/pdb |
| 分子名称 | Pv cell-traversal protein, 7g7 heavy chain, 7g7 light chain, ... (4 entities in total) |
| 機能のキーワード | cell-traversal protein, ookinetes, sporozoites, transmission-blocking, membrane disruption, cell invasion |
| 由来する生物種 | Plasmodium vivax (malaria parasite P. vivax) 詳細 |
| タンパク質・核酸の鎖数 | 12 |
| 化学式量合計 | 282498.76 |
| 構造登録者 | |
| 主引用文献 | Tang, W.K.,Salinas, N.D.,Kolli, S.K.,Xu, S.,Urusova, D.V.,Kumar, H.,Jimah, J.R.,Subramani, P.A.,Ogbondah, M.M.,Barnes, S.J.,Adams, J.H.,Tolia, N.H. Multistage protective anti-CelTOS monoclonal antibodies with cross-species sterile protection against malaria. Nat Commun, 15:7487-7487, 2024 Cited by PubMed Abstract: CelTOS is a malaria vaccine antigen that is conserved in Plasmodium and other apicomplexan parasites and plays a role in cell-traversal. The structural basis and mechanisms of CelTOS-induced protective immunity to parasites are unknown. Here, CelTOS-specific monoclonal antibodies (mAbs) 7g7 and 4h12 demonstrated multistage activity, protecting against liver infection and preventing parasite transmission to mosquitoes. Both mAbs demonstrated cross-species activity with sterile protection against in vivo challenge with transgenic parasites containing either P. falciparum or P. vivax CelTOS, and with transmission reducing activity against P. falciparum. The mAbs prevented CelTOS-mediated pore formation providing insight into the protective mechanisms. X-ray crystallography and mutant-library epitope mapping revealed two distinct broadly conserved neutralizing epitopes. 7g7 bound to a parallel dimer of CelTOS, while 4h12 bound to a novel antiparallel dimer architecture. These findings inform the design of antibody therapies and vaccines and raise the prospect of a single intervention to simultaneously combat P. falciparum and P. vivax malaria. PubMed: 39209843DOI: 10.1038/s41467-024-51701-2 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (3.2 Å) |
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