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

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 pre...

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Detalles Bibliográficos
Autores principales: Malet, Hélène, Dalle, Karen, Brémond, Nicolas, Tocque, Fabienne, Blangy, Stéphanie, Campanacci, Valérie, Coutard, Bruno, Grisel, Sacha, Lichière, Julie, Lantez, Violaine, Cambillau, Christian, Canard, Bruno, Egloff, Marie-Pierre
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222557/
https://www.ncbi.nlm.nih.gov/pubmed/16582497
http://dx.doi.org/10.1107/S1744309106009274
Descripción
Sumario: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 Å, β = 91.4°, and the asymmetric unit contains either two or three molecules. Both native and selenomethionine-labelled crystals diffract to 1.8 Å.