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Expression, purification and molecular modeling of the NIa protease of Cardamom mosaic virus.

Authors :
Jebasingh T
Pandaranayaka EP
Mahalakshmi A
Kasin Yadunandam A
Krishnaswamy S
Usha R
Source :
Journal of biomolecular structure & dynamics [J Biomol Struct Dyn] 2013; Vol. 31 (6), pp. 602-11. Date of Electronic Publication: 2012 Aug 13.
Publication Year :
2013

Abstract

The NIa protease of Potyviridae is the major viral protease that processes potyviral polyproteins. The NIa protease coding region of Cardamom mosaic virus (CdMV) is amplified from the viral cDNA, cloned and expressed in Escherichia coli. NIa protease forms inclusion bodies in E.coli. The inclusion bodies are solubilized with 8 M urea, refolded and purified by Nickel-Nitrilotriacetic acid affinity chromatography. Three-dimensional modeling of the CdMV NIa protease is achieved by threading approach using the homologous X-ray crystallographic structure of Tobacco etch mosaic virus NIa protease. The model gave an insight in to the substrate specificities of the NIa proteases and predicted the complementation of nearby residues in the catalytic triad (H42, D74 and C141) mutants in the cis protease activity of CdMV NIa protease.

Details

Language :
English
ISSN :
1538-0254
Volume :
31
Issue :
6
Database :
MEDLINE
Journal :
Journal of biomolecular structure & dynamics
Publication Type :
Academic Journal
Accession number :
22888800
Full Text :
https://doi.org/10.1080/07391102.2012.706078