6533b82afe1ef96bd128c40c

RESEARCH PRODUCT

Selenomethionine labeling of large biological macromolecular complexes: probing the structure of marine bacterial virus PM2.

Jonathan M. GrimesJaana K. H. BamfordDennis H. BamfordNicola G. A. AbresciaDavid I. StuartHanna M. Kivelä

subject

0303 health sciencesbiologyStrain (chemistry)030306 microbiologyAuxotrophyCorticoviridaechemistry.chemical_elementCrystallography X-Raybiology.organism_classificationVirusBacteriophage03 medical and health scienceschemistryBiochemistryStructural BiologyYield (chemistry)MethodsBacterial virusSelenomethionineSelenium030304 developmental biologyMacromolecule

description

There is a need for improved tools for labeling protein species within large macromolecular assemblies. Here we describe a method for the efficient selenomethionine labeling of the membrane-containing bacterial virus PM2 for structural studies. By examining potential host cells a strain was found which was auxotrophic for methionine, and by performing a multiparameter search of conditions it was possible to derive a robust protocol which simultaneously minimized the toxic effects of the selenomethionine, so that a reasonable virus yield was maintained, whilst still achieving essentially complete labeling. This has allowed us to fingerprint the protein constituents of the virus in a relatively low resolution electron density map. Such a technique can be adapted to other macromolecule complexes studied by X-ray crystallography.

10.1016/j.jsb.2007.10.013http://ora.ox.ac.uk/objects/uuid:851743d3-1b7e-4fa9-a41f-c2f38671fa03