Literature DB >> 25185582

An extracellular polymer at the interface of magnetic bioseparations.

Vijaykumar L Dhadge1, Patricia I Morgado1, Filomena Freitas1, Maria A Reis1, Ana Azevedo2, Raquel Aires-Barros2, A Cecilia A Roque3.   

Abstract

FucoPol, a fucose-containing extracellular polysaccharide (EPS) produced by bacterium Enterobacter A47 using glycerol as the carbon source, was employed as a coating material for magnetic particles (MPs), which were subsequently functionalized with an artificial ligand for the capture of antibodies. The performance of the modified MPs (MP-EPS-22/8) for antibody purification was investigated using direct magnetic separation alone or combined with an aqueous two-phase system (ATPS) composed of polyethylene glycol (PEG) and dextran. In direct magnetic capturing, and using pure protein solutions of human immunoglobulin G (hIgG) and bovine serum albumin (BSA), MP-EPS-22/8 bound 120 mg hIgG g(-1) MPs, whereas with BSA only 10 ± 2 mg BSA g(-1) MPs was achieved. The hybrid process combining both the ATPS and magnetic capturing leads to a good performance for partitioning of hIgG in the desired phase as well as recovery by the magnetic separator. The MPs were able to bind 145 mg of hIgG g(-1) of particles which is quite high when compared with direct magnetic separation. The theoretical maximum capacity was calculated to be 410 ± 15 mg hIgG adsorbed g(-1) MPs with a binding affinity constant of 4.3 × 10(4) M(-1). In multiple extraction steps, the MPs bound 92% of loaded hIgG with a final purity level of 98.5%. The MPs could easily be regenerated, recycled and re-used for five cycles with only minor loss of capacity. FucoPol coating allowed both electrostatic and hydrophobic interactions with the antibody contributing to enhance the specificity for the targeted products.
© 2014 The Author(s) Published by the Royal Society. All rights reserved.

Entities:  

Keywords:  aqueous two-phase extraction; bacterial extracellular polysaccharide; human antibodies; magnetic particles; magnetic separation; synthetic affinity ligand

Mesh:

Substances:

Year:  2014        PMID: 25185582      PMCID: PMC4191107          DOI: 10.1098/rsif.2014.0743

Source DB:  PubMed          Journal:  J R Soc Interface        ISSN: 1742-5662            Impact factor:   4.118


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