(F)uridylylated Peptides Linked to VPg1 of Foot-and- Mouth Disease Virus (FMDV): Design, Synthesis and X-Ray Crystallography of the Complexes with FMDV RNA-Dependent RNA Polymerase

• Main Authors: Sonia de Castro, Cristina Ferrer-Orta, Alberto Mills, Gloria Fernández-Cureses, Federico Gago, Nuria Verdaguer, María-José Camarasa
• Format: Article
• Language: English
• Published: MDPI AG 2019-06-01
• Series: Molecules
• Subjects: foot-and-mouth disease virus; RNA-dependent RNA polymerase; 5-fluorouracil; uridylylation inhibition; VPg
• Online Access: https://www.mdpi.com/1420-3049/24/13/2360

Foot-and-mouth disease virus (FMDV) is an RNA virus belonging to the <i>Picornaviridae</i> family that contains three small viral proteins (VPgs), named VPg1, VPg2 and VPg3, linked to the 5&#8242;-end of the viral genome. These VPg proteins act as primers for RNA replication, which is initiated by the consecutive binding of two UMP molecules to the hydroxyl group of Tyr3 in VPg. This process, termed uridylylation, is catalyzed by the viral RNA-dependent RNA polymerase named 3D^pol. 5-Fluorouridine triphosphate (FUTP) is a potent competitive inhibitor of VPg uridylylation. Peptide analysis showed FUMP covalently linked to the Tyr3 of VPg. This fluorouridylylation prevents further incorporation of the second UMP residue. The molecular basis of how the incorporated FUMP blocks the incorporation of the second UMP is still unknown. To investigate the mechanism of inhibition of VPg uridylylation by FUMP, we have prepared a simplified 15-mer model of VPg1 containing FUMP and studied its x-ray crystal structure in complex with 3D^pol. Unfortunately, the fluorouridylylated VPg1 was disordered and not visible in the electron density maps; however, the structure of 3D^pol in the presence of VPg1-FUMP showed an 8 &#197; movement of the &#946;9-&#945;11 loop of the polymerase towards the active site cavity relative to the complex of 3D^pol with VPg1-UMP. The conformational rearrangement of this loop preceding the 3D^pol B motif seems to block the access of the template nucleotide to the catalytic cavity. This result may be useful in the design of new antivirals against not only FMDV but also other picornaviruses, since all members of this family require the uridylylation of their VPg proteins to initiate the viral RNA synthesis.