Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

9N6U

Crystal structure of 18F25 malarial antibody

Summary for 9N6U
Entry DOI10.2210/pdb9n6u/pdb
Descriptor18F25 Heavy Chain, 18F25 Kappa Chain, SULFATE ION, ... (4 entities in total)
Functional Keywordsantibody, malaria, immune system
Biological sourceMus musculus (mouse)
More
Total number of polymer chains2
Total formula weight47400.66
Authors
Yoo, R.,Julien, J.P. (deposition date: 2025-02-05, release date: 2025-10-15, Last modification date: 2025-11-19)
Primary citationBekkering, E.T.,Yoo, R.,Hailemariam, S.,Heide, F.,Ivanochko, D.,Jackman, M.,Proellochs, N.I.,Stoter, R.,van Gemert, G.J.,Maeda, A.,Yuguchi, T.,Wanders, O.T.,van Daalen, R.C.,Inklaar, M.R.,Andrade, C.M.,Jansen, P.W.T.C.,Vermeulen, M.,Bousema, T.,Takashima, E.,Rubinstein, J.L.,Kooij, T.W.A.,Jore, M.M.,Julien, J.P.
Cryo-EM structure of endogenous Pfs230:Pfs48/45 complex with six antibodies reveals mechanisms of malaria transmission-blocking activity.
Immunity, 58:2899-2916.e10, 2025
Cited by
PubMed Abstract: The Pfs230:Pfs48/45 complex forms the basis for leading malaria transmission-blocking vaccine candidates, yet little is known about its molecular assembly. Here, we used cryo-electron microscopy to elucidate the structure of the endogenous Pfs230:Pfs48/45 complex bound to six transmission-blocking antibodies. Our structure revealed that Pfs230 consists of multiple domain clusters rigidified by interactions mediated through insertion domains. Membrane-anchored Pfs48/45 formed a disk-like structure, interacting with a short C-terminal peptide on Pfs230 that was critical for Pfs230 membrane-retention in vivo. Membrane retention through this interaction was not essential for transmission to mosquitoes, suggesting that complex disruption is not a mode of action for transmission-blocking antibodies. Analyses of Pfs48/45- and Pfs230-targeted antibodies identified conserved epitopes on the Pfs230:Pfs48/45 complex and provided a structural paradigm for complement-dependent activity of Pfs230-targeting antibodies. Altogether, the antibody-bound Pfs230:Pfs48/45 structure improves our molecular understanding of this biological complex, informing the development of next-generation Plasmodium falciparum transmission-blocking interventions.
PubMed: 41072404
DOI: 10.1016/j.immuni.2025.09.014
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.6 Å)
Structure validation

250359

PDB entries from 2026-03-11

PDB statisticsPDBj update infoContact PDBjnumon