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The effect of polymer end-group on the formation of styrene - maleic acid lipid particles (SMALPs)

Neville, George M. ; Morrison, Kerrie A. ; Shilliday, Ella R. ; Doutch, James ; Dalgliesh, Robert ; Price, Gareth J. and Edler, Karen J. LU orcid (2023) In Soft Matter 19(44). p.8507-8518
Abstract

A series of block copolymers comprising styrene and maleic acid (SMA) has been prepared using RAFT polymerisation. RAFT often results in a large hydrophobic alkylthiocarbonylthio end group and this work examines its effect on the solution behaviour of the copolymers. SMA variants with, and without, this end group were synthesised and their behaviour compared with a commercially-available random copolymer of similar molecular weight. Dynamic light scattering and surface tension measurements found the RAFT-copolymers preferentially self-assembled into higher-order aggregates in aqueous solution. Small angle neutron scattering using deuterated styrene varients add support to the accepted model that these agreggates comprise a... (More)

A series of block copolymers comprising styrene and maleic acid (SMA) has been prepared using RAFT polymerisation. RAFT often results in a large hydrophobic alkylthiocarbonylthio end group and this work examines its effect on the solution behaviour of the copolymers. SMA variants with, and without, this end group were synthesised and their behaviour compared with a commercially-available random copolymer of similar molecular weight. Dynamic light scattering and surface tension measurements found the RAFT-copolymers preferentially self-assembled into higher-order aggregates in aqueous solution. Small angle neutron scattering using deuterated styrene varients add support to the accepted model that these agreggates comprise a solvent-protected styrenic core with an acid-rich shell. Replacing the hydrophobic RAFT end group with a more hydrophilic nitrile caused differences in the resulting surface activity, attributed to the ability of the adjoining styrene homoblock to drive aggregation. Each of the copolymers formed SMALP nanodiscs with DMPC lipids, which were found to encapsulate a model membrane protein, gramicidin. However, end group variation affected solubilisition of DPPC, a lipid with a higher phase transition temperature. When using RAFT-copolymers terminated with a hydrophobic group, swelling of the bilayer and greater penetration of the homoblock into the nanodisc core occurred with increasing homoblock length. Conversely, commercial and nitrile-terminated RAFT-copolymers produced nanodisc sizes that stayed constant, instead indicating interaction at the edge of the lipid patch. The results highlight how even minor changes to the copolymer can modify the amphiphilic balance between regions, knowledge useful towards optimising copolymer structure to enhance and control nanodisc formation.

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publishing date
type
Contribution to journal
publication status
published
subject
in
Soft Matter
volume
19
issue
44
pages
12 pages
publisher
Royal Society of Chemistry
external identifiers
  • scopus:85175574237
ISSN
1744-683X
DOI
10.1039/d3sm01180a
language
English
LU publication?
no
id
19028d78-53d8-4f12-a769-3142bf3814d3
date added to LUP
2023-11-13 13:31:03
date last changed
2024-01-10 15:21:20
@article{19028d78-53d8-4f12-a769-3142bf3814d3,
  abstract     = {{<p>A series of block copolymers comprising styrene and maleic acid (SMA) has been prepared using RAFT polymerisation. RAFT often results in a large hydrophobic alkylthiocarbonylthio end group and this work examines its effect on the solution behaviour of the copolymers. SMA variants with, and without, this end group were synthesised and their behaviour compared with a commercially-available random copolymer of similar molecular weight. Dynamic light scattering and surface tension measurements found the RAFT-copolymers preferentially self-assembled into higher-order aggregates in aqueous solution. Small angle neutron scattering using deuterated styrene varients add support to the accepted model that these agreggates comprise a solvent-protected styrenic core with an acid-rich shell. Replacing the hydrophobic RAFT end group with a more hydrophilic nitrile caused differences in the resulting surface activity, attributed to the ability of the adjoining styrene homoblock to drive aggregation. Each of the copolymers formed SMALP nanodiscs with DMPC lipids, which were found to encapsulate a model membrane protein, gramicidin. However, end group variation affected solubilisition of DPPC, a lipid with a higher phase transition temperature. When using RAFT-copolymers terminated with a hydrophobic group, swelling of the bilayer and greater penetration of the homoblock into the nanodisc core occurred with increasing homoblock length. Conversely, commercial and nitrile-terminated RAFT-copolymers produced nanodisc sizes that stayed constant, instead indicating interaction at the edge of the lipid patch. The results highlight how even minor changes to the copolymer can modify the amphiphilic balance between regions, knowledge useful towards optimising copolymer structure to enhance and control nanodisc formation.</p>}},
  author       = {{Neville, George M. and Morrison, Kerrie A. and Shilliday, Ella R. and Doutch, James and Dalgliesh, Robert and Price, Gareth J. and Edler, Karen J.}},
  issn         = {{1744-683X}},
  language     = {{eng}},
  month        = {{10}},
  number       = {{44}},
  pages        = {{8507--8518}},
  publisher    = {{Royal Society of Chemistry}},
  series       = {{Soft Matter}},
  title        = {{The effect of polymer end-group on the formation of styrene - maleic acid lipid particles (SMALPs)}},
  url          = {{http://dx.doi.org/10.1039/d3sm01180a}},
  doi          = {{10.1039/d3sm01180a}},
  volume       = {{19}},
  year         = {{2023}},
}