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Protein partitioning in thermoseparating systems of a charged hydrophobically modified ethylene oxide polymer

Jönsson, Malin LU and Johansson, Hans-Olof LU (2003) In Journal of Chromatography A 983(1-2). p.133-144
Abstract
The phase behavior of a thermoseparating cationic hydrophobically modified ethylene oxide polymer (HM-EO) containing tertiary amines has been investigated at different pH, salt and sodium dodecyl sulfate (SDS) concentrations, in order to find a water/HM-EO two-phase, system suitable for protein partitioning. The used polymer forms micellar aggregates that can be charged. By changing pH and SDS concentrations the netcharge of the SDS/HM-EO aggregate can be shifted from positive to negative. Bovine serum albumin (BSA) and lysozyme were partitioned in the thermoseparated two-phase systems of the cationic polymer at different pH, salt and SDS concentrations. The dominant attractive interactions between the polymer aggregates and the studied... (More)
The phase behavior of a thermoseparating cationic hydrophobically modified ethylene oxide polymer (HM-EO) containing tertiary amines has been investigated at different pH, salt and sodium dodecyl sulfate (SDS) concentrations, in order to find a water/HM-EO two-phase, system suitable for protein partitioning. The used polymer forms micellar aggregates that can be charged. By changing pH and SDS concentrations the netcharge of the SDS/HM-EO aggregate can be shifted from positive to negative. Bovine serum albumin (BSA) and lysozyme were partitioned in the thermoseparated two-phase systems of the cationic polymer at different pH, salt and SDS concentrations. The dominant attractive interactions between the polymer aggregates and the studied proteins were shown to be of electrostatic (Coulomb) nature rather than hydrophobic interaction. At low ionic strength the positively charged polymeric aggregates attracted negatively charged BSA and repelled positively charged lysozyme. Upon addition of SDS the negatively charged aggregates attracted lysozyme and repelled BSA. Thus, it was possible to direct proteins with different charges to the polymeric phase and redirect them to a polymer-depleted phase by changing the netcharge of the polymeric aggregates. The effect of different salts on the partitioning of BSA in a system of slightly positively charged HM-EO was studied. NaCl and KBr have a significant effect on driving the BSA to the polymer-depleted phase, whereas KF and K2SO4 have a smaller effect on the partitioning. The cloud point temperature of the charged polymer decreased upon addition of SDS near the isoelectric molar ratio of SDS to polymer and also upon salt addition. In the latter case the decrease was smaller than expected from model calculations based on Flory-Huggins theory, which were performed for a charged thermoseparating polymer at different charges and salt concentrations. (C) 2002 Elsevier Science B.V. All rights reserved. (Less)
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author
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type
Contribution to journal
publication status
published
subject
keywords
poly(ethylene oxide), proteins, protein partitioning, thermoseparation modelling, aqueous two-phase systems, mixed micelles, temperature effects
in
Journal of Chromatography A
volume
983
issue
1-2
pages
133 - 144
publisher
Elsevier
external identifiers
  • pmid:12568377
  • wos:000180309500012
  • scopus:1842833338
ISSN
0021-9673
DOI
10.1016/S0021-9673(02)01695-3
language
English
LU publication?
yes
id
f8b25ffd-e27a-4bd3-8ea4-24811f1bdeb0 (old id 320357)
date added to LUP
2016-04-01 16:09:32
date last changed
2022-04-15 02:32:46
@article{f8b25ffd-e27a-4bd3-8ea4-24811f1bdeb0,
  abstract     = {{The phase behavior of a thermoseparating cationic hydrophobically modified ethylene oxide polymer (HM-EO) containing tertiary amines has been investigated at different pH, salt and sodium dodecyl sulfate (SDS) concentrations, in order to find a water/HM-EO two-phase, system suitable for protein partitioning. The used polymer forms micellar aggregates that can be charged. By changing pH and SDS concentrations the netcharge of the SDS/HM-EO aggregate can be shifted from positive to negative. Bovine serum albumin (BSA) and lysozyme were partitioned in the thermoseparated two-phase systems of the cationic polymer at different pH, salt and SDS concentrations. The dominant attractive interactions between the polymer aggregates and the studied proteins were shown to be of electrostatic (Coulomb) nature rather than hydrophobic interaction. At low ionic strength the positively charged polymeric aggregates attracted negatively charged BSA and repelled positively charged lysozyme. Upon addition of SDS the negatively charged aggregates attracted lysozyme and repelled BSA. Thus, it was possible to direct proteins with different charges to the polymeric phase and redirect them to a polymer-depleted phase by changing the netcharge of the polymeric aggregates. The effect of different salts on the partitioning of BSA in a system of slightly positively charged HM-EO was studied. NaCl and KBr have a significant effect on driving the BSA to the polymer-depleted phase, whereas KF and K2SO4 have a smaller effect on the partitioning. The cloud point temperature of the charged polymer decreased upon addition of SDS near the isoelectric molar ratio of SDS to polymer and also upon salt addition. In the latter case the decrease was smaller than expected from model calculations based on Flory-Huggins theory, which were performed for a charged thermoseparating polymer at different charges and salt concentrations. (C) 2002 Elsevier Science B.V. All rights reserved.}},
  author       = {{Jönsson, Malin and Johansson, Hans-Olof}},
  issn         = {{0021-9673}},
  keywords     = {{poly(ethylene oxide); proteins; protein partitioning; thermoseparation modelling; aqueous two-phase systems; mixed micelles; temperature effects}},
  language     = {{eng}},
  number       = {{1-2}},
  pages        = {{133--144}},
  publisher    = {{Elsevier}},
  series       = {{Journal of Chromatography A}},
  title        = {{Protein partitioning in thermoseparating systems of a charged hydrophobically modified ethylene oxide polymer}},
  url          = {{http://dx.doi.org/10.1016/S0021-9673(02)01695-3}},
  doi          = {{10.1016/S0021-9673(02)01695-3}},
  volume       = {{983}},
  year         = {{2003}},
}