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8FE4

Structure of dengue virus (DENV2) in complex with prM13, an anti-PrM monoclonal antibody

Summary for 8FE4
Entry DOI10.2210/pdb8fe4/pdb
EMDB information29021
DescriptorEnvelope protein E, prM protein, prM13 Fab Heavy Chain, ... (4 entities in total)
Functional Keywordsdenv, flavivirus, prm antibody, prm13, virus-immune system complex, virus/immune system
Biological sourceDengue virus type 2
More
Total number of polymer chains12
Total formula weight300531.50
Authors
Primary citationA Dowd, K.,Sirohi, D.,D Speer, S.,VanBlargan, L.A.,Chen, R.E.,Mukherjee, S.,Whitener, B.M.,Govero, J.,Aleshnick, M.,Larman, B.,Sukupolvi-Petty, S.,Sevvana, M.,Miller, A.S.,Klose, T.,Zheng, A.,Koenig, S.,Kielian, M.,Kuhn, R.J.,Diamond, M.S.,Pierson, T.C.
prM-reactive antibodies reveal a role for partially mature virions in dengue virus pathogenesis.
Proc.Natl.Acad.Sci.USA, 120:e2218899120-e2218899120, 2023
Cited by
PubMed Abstract: Cleavage of the flavivirus premembrane (prM) structural protein during maturation can be inefficient. The contribution of partially mature flavivirus virions that retain uncleaved prM to pathogenesis during primary infection is unknown. To investigate this question, we characterized the functional properties of newly-generated dengue virus (DENV) prM-reactive monoclonal antibodies (mAbs) in vitro and using a mouse model of DENV disease. Anti-prM mAbs neutralized DENV infection in a virion maturation state-dependent manner. Alanine scanning mutagenesis and cryoelectron microscopy of anti-prM mAbs in complex with immature DENV defined two modes of attachment to a single antigenic site. In vivo, passive transfer of intact anti-prM mAbs resulted in an antibody-dependent enhancement of disease. However, protection against DENV-induced lethality was observed when the transferred mAbs were genetically modified to inhibit their ability to interact with Fcγ receptors. These data establish that in addition to mature forms of the virus, partially mature infectious prM virions can also contribute to pathogenesis during primary DENV infections.
PubMed: 36638211
DOI: 10.1073/pnas.2218899120
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (9.8 Å)
Structure validation

226707

數據於2024-10-30公開中

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