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8TYC

Lassa GPC (strain Josiah) bound to rabbit polyclonal base-targeting antibody Base-1

Summary for 8TYC
Entry DOI10.2210/pdb8tyc/pdb
EMDB information41713
DescriptorGlycoprotein G1, 2-acetamido-2-deoxy-beta-D-glucopyranose, Polyclonal antibody Base-1 heavy chain, ... (10 entities in total)
Functional Keywordslassa virus glycoprotein complex, gpc, immune complex, antibody, polyclonal antibody, base antibody, viral protein, viral protein-immune system complex, viral protein/immune system
Biological sourceLassa virus
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Total number of polymer chains8
Total formula weight255615.62
Authors
Perrett, H.R.,Brouwer, P.J.M.,Ward, A.B. (deposition date: 2023-08-24, release date: 2024-09-11, Last modification date: 2025-04-09)
Primary citationBrouwer, P.J.M.,Perrett, H.R.,Beaumont, T.,Nijhuis, H.,Kruijer, S.,Burger, J.A.,Bontjer, I.,Lee, W.H.,Ferguson, J.A.,Schauflinger, M.,Muller-Krauter, H.,Sanders, R.W.,Strecker, T.,van Gils, M.J.,Ward, A.B.
Defining bottlenecks and opportunities for Lassa virus neutralization by structural profiling of vaccine-induced polyclonal antibody responses.
Cell Rep, 43:114708-114708, 2024
Cited by
PubMed Abstract: Lassa fever continues to be a major public health burden in West Africa, yet effective therapies or vaccines are lacking. The isolation of protective neutralizing antibodies against the Lassa virus glycoprotein complex (GPC) justifies the development of vaccines that can elicit strong neutralizing antibody responses. However, Lassa vaccine candidates have generally been unsuccessful at doing so, and the associated antibody responses to these vaccines remain poorly characterized. Here, we establish an electron microscopy-based epitope mapping workflow that enables high-resolution structural characterization of polyclonal antibodies to the GPC. By applying this method to rabbits vaccinated with a recombinant GPC vaccine and a GPC-derived virus-like particle, we reveal determinants of neutralization that involve epitopes of the GPC-A competition cluster. Furthermore, by identifying undescribed immunogenic off-target epitopes, we expose the challenges that recombinant GPC vaccines face. By enabling detailed polyclonal antibody characterization, our work ushers in a next generation of more rational Lassa vaccine design.
PubMed: 39243373
DOI: 10.1016/j.celrep.2024.114708
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.3 Å)
Structure validation

237735

數據於2025-06-18公開中

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