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7RQQ

Structure of chimeric antibody F10heavy_L9light with PfCSP peptide NANPNVDP

Summary for 7RQQ
Entry DOI10.2210/pdb7rqq/pdb
Related7RQP
DescriptorF10 Heavy Chain, L9 Kappa Chain, PfCSP peptide NANPNVDP, ... (6 entities in total)
Functional Keywordsmalaria, antibody, immune system
Biological sourceHomo sapiens
More
Total number of polymer chains3
Total formula weight49193.68
Authors
Hurlburt, N.K.,Pancera, M. (deposition date: 2021-08-06, release date: 2022-03-02, Last modification date: 2024-10-30)
Primary citationWang, L.T.,Hurlburt, N.K.,Schon, A.,Flynn, B.J.,Flores-Garcia, Y.,Pereira, L.S.,Kiyuka, P.K.,Dillon, M.,Bonilla, B.,Zavala, F.,Idris, A.H.,Francica, J.R.,Pancera, M.,Seder, R.A.
The light chain of the L9 antibody is critical for binding circumsporozoite protein minor repeats and preventing malaria.
Cell Rep, 38:110367-110367, 2022
Cited by
PubMed Abstract: L9 is a potent human monoclonal antibody (mAb) that preferentially binds two adjacent NVDP minor repeats and cross-reacts with NANP major repeats of the Plasmodium falciparum circumsporozoite protein (PfCSP) on malaria-infective sporozoites. Understanding this mAb's ontogeny and mechanisms of binding PfCSP will facilitate vaccine development. Here, we isolate mAbs clonally related to L9 and show that this B cell lineage has baseline NVDP affinity and evolves to acquire NANP reactivity. Pairing the L9 kappa light chain (L9κ) with clonally related heavy chains results in chimeric mAbs that cross-link two NVDPs, cross-react with NANP, and more potently neutralize sporozoites in vivo compared with their original light chain. Structural analyses reveal that the chimeric mAbs bound minor repeats in a type-1 β-turn seen in other repeat-specific antibodies. These data highlight the importance of L9κ in binding NVDP on PfCSP to neutralize sporozoites and suggest that PfCSP-based immunogens might be improved by presenting ≥2 NVDPs.
PubMed: 35172158
DOI: 10.1016/j.celrep.2022.110367
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.89 Å)
Structure validation

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