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8VVL

CCHFV GP38 bound to c13G8 Fab

Summary for 8VVL
Entry DOI10.2210/pdb8vvl/pdb
DescriptorGP38, c13G8 Fab Heavy Chain, c13G8 Fab Light Chain, ... (9 entities in total)
Functional Keywordscchfv, gp38, antibody, immunology, viral protein, viral protein-immune system complex, viral protein/immune system
Biological sourceCrimean-Congo hemorrhagic fever virus
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Total number of polymer chains3
Total formula weight79077.43
Authors
Hjorth, C.K.,Mishra, A.K.,McLellan, J.S. (deposition date: 2024-01-31, release date: 2024-07-17, Last modification date: 2024-10-16)
Primary citationShin, O.S.,Monticelli, S.R.,Hjorth, C.K.,Hornet, V.,Doyle, M.,Abelson, D.,Kuehne, A.I.,Wang, A.,Bakken, R.R.,Mishra, A.K.,Middlecamp, M.,Champney, E.,Stuart, L.,Maurer, D.P.,Li, J.,Berrigan, J.,Barajas, J.,Balinandi, S.,Lutwama, J.J.,Lobel, L.,Zeitlin, L.,Walker, L.M.,Dye, J.M.,Chandran, K.,Herbert, A.S.,Pauli, N.T.,McLellan, J.S.
Crimean-Congo hemorrhagic fever survivors elicit protective non-neutralizing antibodies that target 11 overlapping regions on glycoprotein GP38.
Cell Rep, 43:114502-114502, 2024
Cited by
PubMed Abstract: Crimean-Congo hemorrhagic fever virus can cause lethal disease in humans yet there are no approved medical countermeasures. Viral glycoprotein GP38, exclusive to Nairoviridae, is a target of protective antibodies and is a key antigen in preclinical vaccine candidates. Here, we isolate 188 GP38-specific antibodies from human survivors of infection. Competition experiments show that these antibodies bind across 5 distinct antigenic sites, encompassing 11 overlapping regions. Additionally, we show structures of GP38 bound with 9 of these antibodies targeting different antigenic sites. Although these GP38-specific antibodies are non-neutralizing, several display protective efficacy equal to or better than murine antibody 13G8 in two highly stringent rodent models of infection. Together, these data expand our understanding regarding this important viral protein and may inform the development of broadly effective CCHFV antibody therapeutics.
PubMed: 39002130
DOI: 10.1016/j.celrep.2024.114502
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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PDB entries from 2024-11-06

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