Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16227
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dc.contributor.authorEarnest-Silveira, Linda-
dc.contributor.authorChristiansen, Dale-
dc.contributor.authorHerrmann, S-
dc.contributor.authorRalph, SA-
dc.contributor.authorDas, S-
dc.contributor.authorGowans, EJ-
dc.contributor.authorTorresi, Joseph-
dc.date2016-06-29-
dc.date.accessioned2016-09-12T06:03:04Z-
dc.date.available2016-09-12T06:03:04Z-
dc.date.issued2016-10-
dc.identifier.citationJournal of Virological Methods 2016; 236: 87-92en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16227-
dc.description.abstractA method for the large-scale production of a quadrivalent mammalian cell derived hepatitis C virus-like particles (HCV VLPs) is described. The HCV core E1 and E2 coding sequences of genotype 1a, 1b, 2a or 3a were co-expressed in Huh7 cell factories using a recombinant adenoviral expression system. The structural proteins self-assembled into VLPs that were purified from Huh7 cell lysates by iodixanol ultracentrifugation and Stirred cell ultrafiltration. Electron microscopy, revealed VLPs of the different genotypes that are morphologically similar. Our results show that it is possible to produce large quantities of individual HCV genotype VLPs with relative ease thus making this approach an alternative for the manufacture of a quadrivalent mammalian cell derived HCV VLP vaccine.en_US
dc.subjectHepatitis Cen_US
dc.subjectQuadrivalent vaccineen_US
dc.subjectVirus-like particlesen_US
dc.titleLarge scale production of a mammalian cell derived quadrivalent hepatitis C virus like particle vaccineen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Virological Methodsen_US
dc.identifier.affiliationAustin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Surgery, Austin Health, the University of Melbourne, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Biochemistry and Molecular Biology, Bio21 Institute of Molecular Science and Biotechnology, The University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, Karnataka, Indiaen_US
dc.identifier.affiliationThe Basil Hetzel Institute and Queen Elizabeth Hospital, University of Adelaide, South Australia, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/27373602en_US
dc.identifier.doi10.1016/j.jviromet.2016.06.012en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-8212-0887en_US
dc.type.austinJournal Articleen_US
local.name.researcherTorresi, Joseph
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptInfectious Diseases-
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