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Merck

Assembly of hybrid bacteriophage Qbeta virus-like particles.

Biochemistry (2009-10-24)
Steven D Brown, Jason D Fiedler, M G Finn
摘要

Bacteriophage Qbeta coat protein forms uniform virus-like particles when expressed recombinantly in a variety of organisms. We have inserted the IgG-binding Z domain at the carboxy terminus of the coat protein and coexpressed this chimeric subunit with native coat protein to create hybrid, IgG-binding virus-like particles. Extracellular osmolytes were found to have an effect on the efficiency of incorporation of fusion proteins into VLPs in Escherichia coli when a carbenicillin, but not a kanamycin, selection marker was used. The addition of sucrose to the growth medium decreased the incorporation efficiency; the osmoprotectant glycine betaine eliminated this effect. The decrease in efficiency was not observed when carbenicillin was omitted from the final expression culture. The addition of sodium chloride instead of sucrose gave rise to particles with a larger number of fusion proteins than the standard conditions. These results illustrate that cellular conditions should be taken into account even in apparently simple systems when natural or engineered protein nanoparticles are made.

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Sigma-Aldrich
羧苄青霉素 二钠盐, BioReagent, suitable for plant cell culture
Sigma-Aldrich
羧苄青霉素 二钠盐, 89.0-100.5% anhydrous basis
Sigma-Aldrich
羧苄青霉素 二钠, meets USP testing specifications