4ghl | pdb_00004ghl

Structural Basis for Marburg virus VP35 mediate immune evasion mechanisms

spinqualitylabelsall models 4ghl, resolution 2.02Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 4ghl is a 6 chain structure with sequence from Lake victoria marburg virus - popp. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Ligands: CL, EDO, MG Related: 3fke, 3l25, 3l26, 3l27, 3l28, 3l29 Gene: Polymerase cofactor VP35, VP35 (Lake Victoria marburg virus - Popp) Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function [VP35_MABVP] Acts as a polymerase cofactor in the RNA polymerase transcription and replication complex. Publication Abstract from PubMed Filoviruses, marburgvirus (MARV) and ebolavirus (EBOV), are causative agents of highly lethal hemorrhagic fever in humans. MARV and EBOV share a common genome organization but show important differences in replication complex formation, cell entry, host tropism, transcriptional regulation, and immune evasion. Multifunctional filoviral viral protein (VP) 35 proteins inhibit innate immune responses. Recent studies suggest double-stranded (ds)RNA sequestration is a potential mechanism that allows EBOV VP35 to antagonize retinoic-acid inducible gene-I (RIG-I) like receptors (RLRs) that are activated by viral pathogen-associated molecular patterns (PAMPs), such as double-strandedness and dsRNA blunt ends. Here, we show that MARV VP35 can inhibit IFN production at multiple steps in the signaling pathways downstream of RLRs. The crystal structure of MARV VP35 IID in complex with 18-bp dsRNA reveals that despite the similar protein fold as EBOV VP35 IID, MARV VP35 IID interacts with the dsRNA backbone and not with blunt ends. Functional studies show that MARV VP35 can inhibit dsRNA-dependent RLR activation and interferon (IFN) regulatory factor 3 (IRF3) phosphorylation by IFN kinases TRAF family member-associated NFkb activator (TANK) binding kinase-1 (TBK-1) and IFN kB kinase e (IKKe) in cell-based studies. We also show that MARV VP35 can only inhibit RIG-I and melanoma differentiation associated gene 5 (MDA5) activation by double strandedness of RNA PAMPs (coating backbone) but is unable to inhibit activation of RLRs by dsRNA blunt ends (end capping). In contrast, EBOV VP35 can inhibit activation by both PAMPs. Insights on differential PAMP recognition and inhibition of IFN induction by a similar filoviral VP35 fold, as shown here, reveal the structural and functional plasticity of a highly conserved virulence factor. Structural basis for Marburg virus VP35-mediated immune evasion mechanisms.,Ramanan P, Edwards MR, Shabman RS, Leung DW, Endlich-Frazier AC, Borek DM, Otwinowski Z, Liu G, Huh J, Basler CF, Amarasinghe GK Proc Natl Acad Sci U S A. 2012 Dec 11;109(50):20661-6. doi:, 10.1073/pnas.1213559109. Epub 2012 Nov 26. PMID:23185024 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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