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7UI1

Pfs230 D1D2 domain in complex with 230AL-37

Summary for 7UI1
Entry DOI10.2210/pdb7ui1/pdb
DescriptorGametocyte surface protein P230, 230AL-37, SULFATE ION (3 entities in total)
Functional Keywordsantibody, plasmodium falciparum, pfs230, transmission blocking, cell invasion
Biological sourcePlasmodium falciparum (malaria parasite P. falciparum)
More
Total number of polymer chains8
Total formula weight273766.94
Authors
Tang, W.K.,Tolia, N.H. (deposition date: 2022-03-28, release date: 2023-02-15, Last modification date: 2023-10-25)
Primary citationTang, W.K.,Coelho, C.H.,Miura, K.,Nguemwo Tentokam, B.C.,Salinas, N.D.,Narum, D.L.,Healy, S.A.,Sagara, I.,Long, C.A.,Duffy, P.E.,Tolia, N.H.
A human antibody epitope map of Pfs230D1 derived from analysis of individuals vaccinated with a malaria transmission-blocking vaccine.
Immunity, 56:433-443.e5, 2023
Cited by
PubMed Abstract: Pfs230 domain 1 (Pfs230D1) is an advanced malaria transmission-blocking vaccine antigen demonstrating high functional activity in clinical trials. However, the structural and functional correlates of transmission-blocking activity are not defined. Here, we characterized a panel of human monoclonal antibodies (hmAbs) elicited in vaccinees immunized with Pfs230D1. These hmAbs exhibited diverse transmission-reducing activity, yet all bound to Pfs230D1 with nanomolar affinity. We compiled epitope-binning data for seventeen hmAbs and structures of nine hmAbs complexes to construct a high-resolution epitope map and revealed that potent transmission-reducing hmAbs bound to one face of Pfs230D1, while non-potent hmAbs bound to the opposing side. The structure of Pfs230D1D2 revealed that non-potent transmission-reducing epitopes were occluded by the second domain. The hmAb epitope map delineated binary hmAb combinations that synergized for extremely high-potency, transmission-reducing activity. This work provides a high-resolution guide for structure-based design of enhanced immunogens and informs diagnostics that measure the transmission-reducing response.
PubMed: 36792576
DOI: 10.1016/j.immuni.2023.01.012
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.3 Å)
Structure validation

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