» Articles » PMID: 20971490

Identification of Tolerated Insertion Sites in Poliovirus Non-structural Proteins

Overview
Journal Virology
Specialty Microbiology
Date 2010 Oct 26
PMID 20971490
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Insertion of nucleotide sequences encoding "tags" that can be expressed in specific viral proteins during an infection is a useful strategy for purifying viral proteins and their functional complexes from infected cells and/or for visualizing the dynamics of their subcellular location over time. To identify regions in the poliovirus polyprotein that could potentially accommodate insertion of tags, transposon-mediated insertion mutagenesis was applied to the entire nonstructural protein-coding region of the poliovirus genome, followed by selection of genomes capable of generating infectious, viable viruses. This procedure allowed us to identify at least one site in each viral nonstructural protein, except protein 2C, in which a minimum of five amino acids could be inserted. The distribution of these sites is analyzed from the perspective of their protein structural context and from the perspective of virus evolution.

Citing Articles

Deep mutation, insertion and deletion scanning across the Enterovirus A proteome reveals constraints shaping viral evolution.

Bakhache W, Symonds-Orr W, McCormick L, Dolan P Nat Microbiol. 2024; 10(1):158-168.

PMID: 39609576 PMC: 11726453. DOI: 10.1038/s41564-024-01871-y.


Uncovering Structural Plasticity of through Deep Insertional and Deletional Scanning.

Bakhache W, Orr W, McCormick L, Dolan P Res Sq. 2024; .

PMID: 38410474 PMC: 10896406. DOI: 10.21203/rs.3.rs-3835307/v1.


A Redundant Mechanism of Recruitment Underlies the Remarkable Plasticity of the Requirement of Poliovirus Replication for the Cellular ArfGEF GBF1.

Viktorova E, Gabaglio S, Meissner J, Lee E, Moghimi S, Sztul E J Virol. 2019; 93(21).

PMID: 31375590 PMC: 6803275. DOI: 10.1128/JVI.00856-19.


Random Insertional Mutagenesis of a Serotype 2 Dengue Virus Clone.

Perry J, Tai A Bio Protoc. 2018; 8(16).

PMID: 30214914 PMC: 6133299. DOI: 10.21769/BioProtoc.2975.


Emergency Services of Viral RNAs: Repair and Remodeling.

Agol V, Gmyl A Microbiol Mol Biol Rev. 2018; 82(2).

PMID: 29540453 PMC: 5968460. DOI: 10.1128/MMBR.00067-17.


References
1.
Mosimann S, Cherney M, Sia S, PLOTCH S, James M . Refined X-ray crystallographic structure of the poliovirus 3C gene product. J Mol Biol. 1998; 273(5):1032-47. DOI: 10.1006/jmbi.1997.1306. View

2.
Baxter N, Roetzer A, Liebig H, Sedelnikova S, Hounslow A, Skern T . Structure and dynamics of coxsackievirus B4 2A proteinase, an enyzme involved in the etiology of heart disease. J Virol. 2006; 80(3):1451-62. PMC: 1346940. DOI: 10.1128/JVI.80.3.1451-1462.2006. View

3.
Schein C, Oezguen N, Volk D, Garimella R, Paul A, Braun W . NMR structure of the viral peptide linked to the genome (VPg) of poliovirus. Peptides. 2006; 27(7):1676-84. PMC: 1629084. DOI: 10.1016/j.peptides.2006.01.018. View

4.
Grant B, Rodrigues A, ElSawy K, McCammon J, Caves L . Bio3d: an R package for the comparative analysis of protein structures. Bioinformatics. 2006; 22(21):2695-6. DOI: 10.1093/bioinformatics/btl461. View

5.
Egger D, Teterina N, EHRENFELD E, Bienz K . Formation of the poliovirus replication complex requires coupled viral translation, vesicle production, and viral RNA synthesis. J Virol. 2000; 74(14):6570-80. PMC: 112167. DOI: 10.1128/jvi.74.14.6570-6580.2000. View