4uce

N-terminal globular domain of the RSV Nucleoprotein in complex with the Nucleoprotein Phosphoprotein interaction inhibitor M72

spinqualitylabelsall models 4uce, resolution 2.95Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 4uce is a 2 chain structure with sequence from Hrsva. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Ligands: MZS, SO4 Related: 4uc6, 4uc7, 4uc8, 4uc9, 4uca, 4ucb, 4ucc, 4ucd Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function [NCAP_HRSVA] Encapsidates the genome, protecting it from nucleases. The nucleocapsid (NC) has a helical structure. The encapsidated genomic RNA is termed the NC and serves as template for transcription and replication. During replication, encapsidation by protein N is coupled to RNA synthesis and all replicative products are resistant to nucleases. Publication Abstract from PubMed Presently, respiratory syncytial virus (RSV), the main cause of severe respiratory infections in infants, cannot be treated efficiently by antivirals. However, its RNA dependent polymerase complex offers potential targets for RSV specific drugs. This includes the recognition of its template, the ribonucleoprotein complex (RNP), consisting of genomic RNA encapsidated by the RSV nucleoprotein N. This recognition proceeds via interaction between the phosphoprotein P, that is the main polymerase co-factor, and N. The determinant role of the C-terminus of P and more particularly of the last residue, F241, in RNP binding and viral RNA synthesis has been assessed previously. Here we provide a detailed structural insight into this crucial interaction for RSV polymerase activity. We solved the crystallographic structure of complexes between the N-terminal domain of N (N-NTD) and C-terminal peptides of P and characterized binding by biophysical approaches. Our results provide a rationale for the pivotal role of F241, which inserts into a well-defined N-NTD pocket. This primary binding site is completed by transient contacts with upstream P residues outside of the pocket. Based on the structural information of the N-NTD:P complex we identified inhibitors of this interaction, selected by in silico screening of small compounds, that efficiently bind to N and compete with P in vitro. One of the compounds displayed inhibitory activity on RSV replication, thereby strengthening the relevance of N-NTD for structure-based design of RSV specific antivirals. IMPORTANCE: Respiratory Syncytial Virus (RSV) is a widespread pathogen that is a leading cause of acute lower respiratory infections in infants worldwide. RSV cannot be treated efficiently by antivirals and no vaccine is presently available, the development of pediatric vaccines being particularly challenging. Therefore there is a need for new therapeutic strategies that specifically target RSV. The interaction between the RSV phosphoprotein P and the ribonucleoprotein complex is critical for viral replication. In this study we identified the main structural determinants of this interaction, and we used them to in silico screen potential inhibitors. We found a family of molecules that were efficient competitors of P in vitro and showed inhibitory activity on RSV replication in cellular assays. These compounds provide a base for a pharmacophore model that must be improved, but holds promises for the design of new RSV specific antivirals. A druggable pocket at the nucleocapsid/phosphoprotein interaction site of the human respiratory syncytial virus.,Ouizougun-Oubari M, Pereira N, Tarus B, Galloux M, Lassoued S, Fix J, Tortorici MA, Hoos S, Baron B, England P, Desmaele D, Couvreur P, Bontems F, Rey FA, Eleouet JF, Sizun C, Slama-Schwok A, Duquerroy S J Virol. 2015 Aug 5. pii: JVI.01612-15. PMID:26246564 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See Also Nucleoprotein

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