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8ULF

Crystal structure of Plasmodium vivax CelTOS in complex with antibody 7g7

Summary for 8ULF
Entry DOI10.2210/pdb8ulf/pdb
DescriptorPv cell-traversal protein, 7g7 heavy chain, 7g7 light chain, ... (4 entities in total)
Functional Keywordscell-traversal protein, ookinetes, sporozoites, transmission-blocking, membrane disruption, cell invasion
Biological sourcePlasmodium vivax (malaria parasite P. vivax)
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Total number of polymer chains12
Total formula weight282498.76
Authors
Tang, W.K.,Tolia, N.H. (deposition date: 2023-10-16, release date: 2024-09-11, Last modification date: 2024-11-13)
Primary citationTang, 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: 39209843
DOI: 10.1038/s41467-024-51701-2
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.2 Å)
Structure validation

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