Back to Search Start Over

Expression, purification and crystallization of the SARS-CoV macro domain.

Authors :
Malet H
Dalle K
Brémond N
Tocque F
Blangy S
Campanacci V
Coutard B
Grisel S
Lichière J
Lantez V
Cambillau C
Canard B
Egloff MP
Source :
Acta crystallographica. Section F, Structural biology and crystallization communications [Acta Crystallogr Sect F Struct Biol Cryst Commun] 2006 Apr 01; Vol. 62 (Pt 4), pp. 405-8. Date of Electronic Publication: 2006 Mar 25.
Publication Year :
2006

Abstract

Macro domains or X domains are found as modules of multidomain proteins, but can also constitute a protein on their own. Recently, biochemical and structural studies of cellular macro domains have been performed, showing that they are active as ADP-ribose-1''-phosphatases. Macro domains are also present in a number of positive-stranded RNA viruses, but their precise function in viral replication is still unknown. The major human pathogen severe acute respiratory syndrome coronavirus (SARS-CoV) encodes 16 non-structural proteins (nsps), one of which (nsp3) encompasses a macro domain. The SARS-CoV nsp3 gene region corresponding to amino acids 182-355 has been cloned, expressed in Escherichia coli, purified and crystallized. The crystals belong to space group P2(1), with unit-cell parameters a = 37.5, b = 55.6, c = 108.9 angstroms, beta = 91.4 degrees, and the asymmetric unit contains either two or three molecules. Both native and selenomethionine-labelled crystals diffract to 1.8 angstroms.

Details

Language :
English
ISSN :
1744-3091
Volume :
62
Issue :
Pt 4
Database :
MEDLINE
Journal :
Acta crystallographica. Section F, Structural biology and crystallization communications
Publication Type :
Academic Journal
Accession number :
16582497
Full Text :
https://doi.org/10.1107/S1744309106009274