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9N5K

Endogenous Pfs230D9-14 in complex with Pfs48/45

Summary for 9N5K
Entry DOI10.2210/pdb9n5k/pdb
Related9N5H 9N5I
EMDB information48921 48922 48924
DescriptorGametocyte surface protein P230, Gametocyte surface protein P45/48 (2 entities in total)
Functional Keywords6-cys, cell adhesion
Biological sourcePlasmodium falciparum 3D7
More
Total number of polymer chains2
Total formula weight415247.64
Authors
Heide, F.,Ivanochko, D.,Bekkering, E.,Yoo, R.,Hailemariam, S.,Julien, J.P. (deposition date: 2025-02-04, release date: 2025-10-15, Last modification date: 2025-10-22)
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.
Structure of endogenous Pfs230:Pfs48/45 in complex with potent malaria transmission-blocking antibodies.
Biorxiv, 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 cryogenic electron microscopy to elucidate the structure of the endogenous Pfs230:Pfs48/45 complex bound to six potent transmission-blocking antibodies. Pfs230 consists of multiple domain clusters rigidified by interactions mediated through insertion domains. Membrane-anchored Pfs48/45 forms a disc-like structure and interacts with a short C-terminal peptide on Pfs230 that is critical for Pfs230 membrane-retention . Interestingly, membrane retention through this interaction is 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 identify conserved epitopes on the Pfs230:Pfs48/45 complex and provides a structural paradigm for complement-dependent activity of Pfs230-targeting antibodies. Altogether, the antibody-bound Pfs230:Pfs48/45 structure presented improves our molecular understanding of this biological complex, informing the development of next-generation transmission-blocking interventions.
PubMed: 39990443
DOI: 10.1101/2025.02.14.638310
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (4.7 Å)
Structure validation

245663

数据于2025-12-03公开中

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