Please use this identifier to cite or link to this item: http://hdl.handle.net/10216/106802
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dc.creatorLeblebici, P
dc.creatorLeblebici, ME
dc.creatorFerreira da Silva, F
dc.creatorAlírio Rodrigues
dc.creatorLuís Pais
dc.date.accessioned2017-09-14T14:11:04Z-
dc.date.available2017-09-14T14:11:04Z-
dc.date.issued2014
dc.identifier.issn1570-0232
dc.identifier.other206100
dc.identifier.urihttp://hdl.handle.net/10216/106802-
dc.description.abstractMonolithic columns have attracted significant attention for the purification of large biomolecules. In the present study, a step gradient elution method was evaluated for the separation of human immunoglobulin G (hIgG) into its subclasses on CIM (convective interaction media) Gamma-protein A (recombinant protein A) monolithic column. hIgG was loaded onto the column and bound protein was eluted with a pH gradient. The subclass content of the eluted fractions was analyzed by enzyme-linked immunosorbent assay (ELISA). Results showed that separation of IgG3 from the other three subclasses can be successfully achieved with high selectivity (100%) and throughput on monolithic media. It was also revealed that enriched fractions of IgG1 and IgG2 could be obtained from purified hIgG in a 28 min long chromatographic run. Three fractions with high IgG1 content (89.1%, 94.3% and 88.8%) were recovered. Furthermore, IgG2 was enriched to 64% successfully. A rapid step gradient elution scheme without any additives in buffers was proven to obtain enriched preparations of the two important subclasses with high throughput. The separation time can be reduced even more by increasing the flow rate without any loss in selectivity, which will be beneficial in industrial scale applications.
dc.language.isoeng
dc.rightsrestrictedAccess
dc.titleSeparation of human immunoglobulin G subclasses on a protein A monolith column
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoFaculdade de Engenharia
dc.identifier.doi10.1016/j.jchromb.2014.05.029
dc.identifier.authenticusP-009-HCF
Appears in Collections:FEUP - Artigo em Revista Científica Internacional

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