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. Kiveläsubject
0303 health sciencesbiologyStrain (chemistry)030306 microbiologyAuxotrophyCorticoviridaechemistry.chemical_elementCrystallography X-Raybiology.organism_classificationVirusBacteriophage03 medical and health scienceschemistryBiochemistryStructural BiologyYield (chemistry)MethodsBacterial virusSelenomethionineSelenium030304 developmental biologyMacromoleculedescription
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.
year | journal | country | edition | language |
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2008-02-01 | Journal of structural biology |