In-solution antibody harvesting with a plant-produced hydrophobin-Protein A fusion

dc.contributorAalto-yliopistofi
dc.contributorAalto Universityen
dc.contributor.authorKurppa, Katri
dc.contributor.authorReuter, Lauri J.
dc.contributor.authorRitala, Anneli
dc.contributor.authorLinder, Markus B.
dc.contributor.authorJoensuu, Jussi J.
dc.contributor.departmentVTT Technical Research Centre of Finland
dc.contributor.departmentDepartment of Biotechnology and Chemical Technology
dc.contributor.departmentDepartment of Bioproducts and Biosystemsen
dc.date.accessioned2017-11-21T13:35:19Z
dc.date.available2017-11-21T13:35:19Z
dc.date.issued2018-02
dc.description.abstractPurification is a bottleneck and a major cost factor in the production of antibodies. We set out to engineer a bifunctional fusion protein from two building blocks, Protein A and a hydrophobin, aiming at low-cost and scalable antibody capturing in solutions. Immunoglobulin-binding Protein A is widely used in affinity-based purification. The hydrophobin fusion tag, on the other hand, has been shown to enable purification by two-phase separation. Protein A was fused to two different hydrophobin tags, HFBI or II, and expressed transiently in Nicotiana benthamiana. The hydrophobins enhanced accumulation up to 35-fold, yielding up to 25% of total soluble protein. Both fused and nonfused Protein A accumulated in protein bodies. Hence, the increased yield could not be attributed to HFB-induced protein body formation. We also demonstrated production of HFBI-Protein A fusion protein in tobacco BY-2 suspension cells in 30 l scale, with a yield of 35 mg/l. Efficient partitioning to the surfactant phase confirmed that the fusion proteins retained the amphipathic properties of the hydrophobin block. The reversible antibody-binding capacity of the Protein A block was similar to the nonfused Protein A. The best-performing fusion protein was tested in capturing antibodies from hybridoma culture supernatant with two-phase separation. The fusion protein was able to carry target antibodies to the surfactant phase and subsequently release them back to the aqueous phase after a change in pH. This report demonstrates the potential of hydrophobin fusion proteins for novel applications, such as harvesting antibodies in solutions.en
dc.description.versionPeer revieweden
dc.format.extent11
dc.format.mimetypeapplication/pdf
dc.identifier.citationKurppa , K , Reuter , L J , Ritala , A , Linder , M B & Joensuu , J J 2018 , ' In-solution antibody harvesting with a plant-produced hydrophobin-Protein A fusion ' , PLANT BIOTECHNOLOGY JOURNAL , vol. 16 , no. 2 , pp. 404-414 . https://doi.org/10.1111/pbi.12780en
dc.identifier.doi10.1111/pbi.12780
dc.identifier.issn1467-7644
dc.identifier.otherPURE UUID: 2c70db28-00c4-4af4-89b8-20527e207e08
dc.identifier.otherPURE ITEMURL: https://research.aalto.fi/en/publications/2c70db28-00c4-4af4-89b8-20527e207e08
dc.identifier.otherPURE LINK: http://www.scopus.com/inward/record.url?scp=85026506807&partnerID=8YFLogxK
dc.identifier.otherPURE FILEURL: https://research.aalto.fi/files/14697006/Kurppa_et_al_2017_Plant_Biotechnology_Journal.pdf
dc.identifier.urihttps://aaltodoc.aalto.fi/handle/123456789/28774
dc.identifier.urnURN:NBN:fi:aalto-201711217595
dc.language.isoenen
dc.relation.ispartofseriesPLANT BIOTECHNOLOGY JOURNALen
dc.rightsopenAccessen
dc.subject.keywordNicotiana benthamiana
dc.subject.keywordAntibody
dc.subject.keywordHydrophobin
dc.subject.keywordProtein A
dc.subject.keywordPurification
dc.subject.keywordTobacco BY-2 suspension cells
dc.titleIn-solution antibody harvesting with a plant-produced hydrophobin-Protein A fusionen
dc.typeA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessäfi
dc.type.versionpublishedVersion
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