Immunoabsorbent Nanoparticles Based on a Tobamovirus Displaying Protein A

Earlier attempts to express peptides longer than 20 aa on the surface of tobamoviruses such as tobacco mosaic virus have failed. Surprisingly, we found that a functional fragment of protein A (133 aa) can be displayed on the surface of a tobamovirus as a C-terminal fusion to the coat protein via a 1...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2006-11, Vol.103 (47), p.17678-17683
Hauptverfasser: Werner, Stefan, Marillonnet, Sylvestre, Hause, Gerd, Klimyuk, Victor, Gleba, Yuri
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Sprache:eng
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Zusammenfassung:Earlier attempts to express peptides longer than 20 aa on the surface of tobamoviruses such as tobacco mosaic virus have failed. Surprisingly, we found that a functional fragment of protein A (133 aa) can be displayed on the surface of a tobamovirus as a C-terminal fusion to the coat protein via a 15-aa linker. The macromolecular nature of these nanoparticles allowed the design of a simple protocol for purification of mAbs with a recovery yield of 50% and >90% product purity. The extremely dense packing of protein A on the nanoparticles (>2,100 copies per viral particle) results in an immunoadsorbent with a binding capacity of 2 g mAb per g. This characteristic, combined with the high level of expression of the nanoparticles (>3 g adsorbent per kg of leaf biomass), provides a very inexpensive self-assembling matrix that could meet the criteria for a single-use industrial immunoadsorbent for antibody purification.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.0608869103