Evidence map›Paper›PMID 29845165›Full record

ArticleNanoscale2018

An acid-compatible co-polymer for the solubilization of membranes and proteins into lipid bilayer-containing nanoparticles.

Stephen C L Hall, Cecilia Tognoloni, Jack Charlton, Éilís C Bragginton, Alice J Rothnie, Pooja Sridhar, Mark Wheatley, Timothy J Knowles, Thomas Arnold, Karen J Edler and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Nanoscale, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
6.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 108 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Advances in native cell membrane nanoparticles system.Current opinion in structural biology · 2025
    Review
  5. Amphiphilic Copolymers and Their Role in the Study of Membrane Proteins.The journal of physical chemistry letters · 2025
    Review
  6. Article
  7. Article
  8. Sulfonated polystyrenes: pH and MgEuropean polymer journal · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Detergent-Free Membrane Protein Purification Using SMA Polymer.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  19. Article
  20. BBA advances · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 3 countries.

Stephen C L HallSchool of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK. t.r.dafforn@bham.ac.uk.
Cecilia Tognoloni
Jack Charlton
Éilís C Bragginton
Alice J Rothnie
Pooja Sridhar
Mark Wheatley
Timothy J Knowles
Thomas Arnold
Karen J Edler
Tim R Dafforn
University of Birmingham · GBUniversity of Bath · GBAston University · GBDiamond Light Source · GBEuropean Spallation Source · SEUniversity of Bristol · GBUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The fundamental importance of membrane proteins in drug discovery has meant that membrane mimetic systems for studying membrane proteins are of increasing interest. One such system has been the amphipathic, negatively charged poly(styrene-co-maleic acid) (SMA) polymer to form "SMA Lipid Particles" (SMALPs) which have been widely adopted to solubilize membrane proteins directly from the cell membrane. However, SMALPs are only soluble under basic conditions and precipitate in the presence of divalent cations required for many downstream applications. Here, we show that the positively charged poly(styrene-co-maleimide) (SMI) forms similar nanoparticles with comparable efficiency to SMA, whilst remaining functional at acidic pH and compatible with high concentrations of divalent cations. We have performed a detailed characterization of the performance of SMI that enables a direct comparison with similar data published for SMA. We also demonstrate that SMI is capable of extracting proteins directly from the cell membrane and can solubilize functional human G-protein coupled receptors (GPCRs) expressed in cultured HEK 293T cells. "SMILPs" thus provide an alternative membrane solubilization method that successfully overcomes some of the limitations of the SMALP method.

Indexed as

HEK293 CellsHumansLipid BilayersMaleatesNanoparticlesPolystyrenesReceptors, G-Protein-CoupledSolubilityLipid BilayersMaleatesPolystyrenesReceptors, G-Protein-Coupledstyrene-maleic acid polymer

Identifiers

PMID29845165
PMCPMC5996351
OpenAlexW2803466132

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.