4WFX

Coxsackievirus B3 Polymerase - F232L Mutant - NaCl Crystal Form

Summary for 4WFX

• Entry DOI: 10.2210/pdb4wfx/pdb
• Related: 3ddk 4WFY 4WFZ
• Descriptor: RNA-directed RNA polymerase, SODIUM ION (3 entities in total)
• Functional Keywords: rna-dependent rna polymerase, transferase
• Biological source: Coxsackievirus B3
• Total number of polymer chains: 1
• Total formula weight: 52534.99

Authors

Peersen, O.B.,McDonald, S.M. (deposition date: 2014-09-17, release date: 2014-10-22, Last modification date: 2023-09-27)

Primary citation

Campagnola, G.,McDonald, S.,Beaucourt, S.,Vignuzzi, M.,Peersen, O.B.
Structure-Function Relationships Underlying the Replication Fidelity of Viral RNA-Dependent RNA Polymerases.
J.Virol., 89:275-286, 2015

PubMed Abstract: Viral RNA-dependent RNA polymerases are considered to be low-fidelity enzymes, providing high mutation rates that allow for the rapid adaptation of RNA viruses to different host cell environments. Fidelity is tuned to provide the proper balance of virus replication rates, pathogenesis, and tissue tropism needed for virus growth. Using our structures of picornaviral polymerase-RNA elongation complexes, we have previously engineered more than a dozen coxsackievirus B3 polymerase mutations that significantly altered virus replication rates and in vivo fidelity and also provided a set of secondary adaptation mutations after tissue culture passage. Here we report a biochemical analysis of these mutations based on rapid stopped-flow kinetics to determine elongation rates and nucleotide discrimination factors. The data show a spatial separation of fidelity and replication rate effects within the polymerase structure. Mutations in the palm domain have the greatest effects on in vitro nucleotide discrimination, and these effects are strongly correlated with elongation rates and in vivo mutation frequencies, with faster polymerases having lower fidelity. Mutations located at the top of the finger domain, on the other hand, primarily affect elongation rates and have relatively minor effects on fidelity. Similar modulation effects are seen in poliovirus polymerase, an inherently lower-fidelity enzyme where analogous mutations increase nucleotide discrimination. These findings further our understanding of viral RNA-dependent RNA polymerase structure-function relationships and suggest that positive-strand RNA viruses retain a unique palm domain-based active-site closure mechanism to fine-tune replication fidelity.

PubMed: 25320316
DOI: 10.1128/JVI.01574-14

Experimental method

X-RAY DIFFRACTION (1.808 Å)