8VMB
The crystal structure of rhinovirus C15 RNA replication element sB-loop mutant in complex with Fab BL3-6
Summary for 8VMB
| Entry DOI | 10.2210/pdb8vmb/pdb |
| Descriptor | RNA (83-MER), Heavy Chain of Fab BL3-6, Light Chain of Fab BL3-6 (3 entities in total) |
| Functional Keywords | enteroviral rna, cloverleaf-like rna, rvc15 rna replication element, enterovirus replication platform, rna-fab complex, rna, rna-immune system complex, rna/immune system |
| Biological source | Homo sapiens More |
| Total number of polymer chains | 3 |
| Total formula weight | 75374.63 |
| Authors | Das, N.K.,Koirala, D. (deposition date: 2024-01-13, release date: 2024-07-24, Last modification date: 2024-10-30) |
| Primary citation | Das, N.K.,Vogt, J.,Patel, A.,Banna, H.A.,Koirala, D. Structural basis for a highly conserved RNA-mediated enteroviral genome replication. Nucleic Acids Res., 52:11218-11233, 2024 Cited by PubMed Abstract: Enteroviruses contain conserved RNA structures at the extreme 5' end of their genomes that recruit essential proteins 3CD and PCBP2 to promote genome replication. However, the high-resolution structures and mechanisms of these replication-linked RNAs (REPLRs) are limited. Here, we determined the crystal structures of the coxsackievirus B3 and rhinoviruses B14 and C15 REPLRs at 1.54, 2.2 and 2.54 Å resolution, revealing a highly conserved H-type four-way junction fold with co-axially stacked sA-sD and sB-sC helices that are stabilized by a long-range A•C•U base-triple. Such conserved features observed in the crystal structures also allowed us to predict the models of several other enteroviral REPLRs using homology modeling, which generated models almost identical to the experimentally determined structures. Moreover, our structure-guided binding studies with recombinantly purified full-length human PCBP2 showed that two previously proposed binding sites, the sB-loop and 3' spacer, reside proximally and bind a single PCBP2. Additionally, the DNA oligos complementary to the 3' spacer, the high-affinity PCBP2 binding site, abrogated its interactions with enteroviral REPLRs, suggesting the critical roles of this single-stranded region in recruiting PCBP2 for enteroviral genome replication and illuminating the promising prospects of developing therapeutics against enteroviral infections targeting this replication platform. PubMed: 39036953DOI: 10.1093/nar/gkae627 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.97 Å) |
Structure validation
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