Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/23752
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dc.contributor.authorSuleman, S-
dc.contributor.authorSchrubaji, K-
dc.contributor.authorFilippou, C-
dc.contributor.authorIgnatova, S-
dc.contributor.authorHewitson, P-
dc.contributor.authorHuddleston, J-
dc.contributor.authorKarda, R-
dc.contributor.authorWaddington, SN-
dc.contributor.authorThemis, M-
dc.date.accessioned2021-12-16T13:26:20Z-
dc.date.available2021-12-16T13:26:20Z-
dc.date.issued2021-10-06-
dc.identifier114305-
dc.identifier.citationSuleman, S., Schrubaji, K., Filippou, C., Ignatova, S., Hewitson, P., Huddleston, J., Karda, R., Waddington, S.N. and Themis, M. (2022) 'Rapid and inexpensive purification of adenovirus vectors using an optimised aqueous two-phase technology', Journal of Virological Methods, 299, 114305, pp. 1-9. doi: 10.1016/j.jviromet.2021.114305.en_US
dc.identifier.issn0166-0934-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/23752-
dc.description.abstractCopyright © 2021 The Author(s). Adenoviruses (AdVs) are used as gene therapy vectors to treat human diseases and as vaccines against COVID-19. AdVs are produced by transfecting human embryonic kidney 239 (HEK293) or PER.C6 virus producer cells with AdV plasmid vectors or infecting these cells withcell lysates containing replication-defective AdV. Cell lysates can be purified further by caesium chloride or chromatographic protocols to research virus seed stocks (RVSS) for characterisation to high quality master virus seed stocks (MVSS) and working virus seed stocks (WVSS) before downstream production of pure, high titre AdV. Lysates are poorly infectious, block filtration columns and have limited storage capability. Aqueous two-phase systems (ATPS) are an alternative method for AdV purification that rapidly generates cleaner RVSS for characterisation to MVSS. After testing multiple ATPS formulations, an aqueous mixture of 20 % PEG 600 and 20 % (NH4)2SO4 (w/w) was found most effective for AdV partitioning, producing up to 97+3% yield of high-titre virus that was devoid of aggregates both effective in vitro and in vivo with no observable cytotoxicity. Importantly, AdV preparations stored at −20 °C or 4 °C show negligible loss of titre and are suitable for downstream processing to clinical grade to support the need for AdV vaccines.en_US
dc.description.sponsorshipBrunel University London Brief award.en_US
dc.format.extent1 - 9-
dc.format.mediumPrint-Electronic-
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.rightsCopyright © 2021 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/).-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectadenovirus type 5en_US
dc.subjectaqueous two-phase partitioning systemen_US
dc.subjectcaesium chlorideen_US
dc.subjectvaccineen_US
dc.subjectviral vector purificationen_US
dc.titleRapid and inexpensive purification of adenovirus vectors using an optimised aqueous two-phase technologyen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1016/j.jviromet.2021.114305-
dc.relation.isPartOfJournal of Virological Methods-
pubs.publication-statusPublished-
pubs.volume299-
dc.identifier.eissn1879-0984-
Appears in Collections:Dept of Life Sciences Research Papers

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