7a57

La Crosse Virus Envelope Glycoprotein Gc W1066H Mutant Fusion Domains in Postfusion Conformation

spinqualitylabelsall models 7a57, resolution 3.15Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 7a57 is a 3 chain structure with sequence from La Crosse virus L78. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 3.155Å Ligands: FUC, NAG Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Publication Abstract from PubMed La Crosse virus, responsible for pediatric encephalitis in the United States, and Schmallenberg virus, a highly teratogenic veterinary virus in Europe, belong to the large Orthobunyavirus genus of zoonotic arthropod-borne pathogens distributed worldwide. Viruses in this under-studied genus cause CNS infections or fever with debilitating arthralgia/myalgia syndromes, with no effective treatment. The main surface antigen, glycoprotein Gc ( approximately 1,000 residues), has a variable N-terminal half (Gc(S)) targeted by the patients' antibody response and a conserved C-terminal moiety (Gc(F)) responsible for membrane fusion during cell entry. Here, we report the X-ray structure of post-fusion La Crosse and Schmallenberg virus Gc(F), revealing the molecular determinants for hairpin formation and trimerization required to drive membrane fusion. We further experimentally confirm the role of residues in the fusion loops and in a vestigial endoplasmic reticulum (ER) translocation sequence at the Gc(S)-Gc(F) junction. The resulting knowledge provides essential molecular underpinnings for future development of potential therapeutic treatments and vaccines. Structure, function, and evolution of the Orthobunyavirus membrane fusion glycoprotein.,Hellert J, Aebischer A, Haouz A, Guardado-Calvo P, Reiche S, Beer M, Rey FA Cell Rep. 2023 Mar 28;42(3):112142. doi: 10.1016/j.celrep.2023.112142. Epub 2023 , Feb 22. PMID:36827185 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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