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8XSE

SARS-CoV-2 RBD + IMCAS-123 + IMCAS-72 Fab

Summary for 8XSE
Entry DOI10.2210/pdb8xse/pdb
EMDB information38617
DescriptorSpike protein S1, IMCAS-123 H chain, IMCAS-123 L chain, ... (6 entities in total)
Functional Keywordssars-cov-2, broadly neutralizing antibodies, virus, viral protein/immune system, viral protein-immune system complex
Biological sourceSevere acute respiratory syndrome coronavirus 2 (2019-nCoV, SARS-CoV-2)
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Total number of polymer chains5
Total formula weight118404.88
Authors
Tong, Z.,Cui, Y.,Xie, Y.,Tong, J.,Gao, G.F.,Qi, J. (deposition date: 2024-01-09, release date: 2024-07-17, Last modification date: 2024-10-23)
Primary citationTong, Z.,Tong, J.,Lei, W.,Xie, Y.,Cui, Y.,Jia, G.,Li, S.,Zhang, Z.,Cheng, Z.,Xing, X.,Ma, H.,Deng, L.,Zhang, R.,Zhao, X.,Liu, K.,Wang, Q.,Qi, J.,Huang, H.,Song, R.,Su, Z.,Wu, G.,Lou, J.,Gao, G.F.
Deciphering a reliable synergistic bispecific strategy of rescuing antibodies for SARS-CoV-2 escape variants, including BA.2.86, EG.5.1, and JN.1.
Cell Rep, 43:114338-114338, 2024
Cited by
PubMed Abstract: The game between therapeutic monoclonal antibodies (mAbs) and continuously emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants has favored the virus, as most therapeutic mAbs have been evaded. Addressing this challenge, we systematically explored a reproducible bispecific antibody (bsAb)-dependent synergistic effect in this study. It could effectively restore the neutralizing activity of the bsAb when any of its single mAbs is escaped by variants. This synergy is primarily attributed to the binding angle of receptor-binding domain (RBD)-5, facilitating inter-spike cross-linking and promoting cryptic epitope exposure that classical antibody cocktails cannot achieve. Furthermore, RBD-5 with RBD-2, RBD-6, and RBD-7, alongside RBD-8, also exhibit significantly enhanced effects. This study not only shifts the paradigm in understanding antibody interactions but paves the way for developing more effective therapeutic antibodies against rapidly mutating SARS-CoV-2, with Dia-19 already showing promise against emerging variants like BA.2.86, EG.5.1, and JN.1.
PubMed: 38850530
DOI: 10.1016/j.celrep.2024.114338
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.5 Å)
Structure validation

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