Abstract
Membrane proteins (MPs) underpin essential cellular processes, representing ~60% of drug targets, but their structural characterisation remains challenging with bottlenecks across production, solubilisation, stabilisation and biophysical analysis. Extraction with detergents can disrupt important protein lipid interactions, impacting structural and mechanistic characterisation. Alternatively, amphiphilic polymers enable direct extraction of MPs with surrounding endogenous lipids forming polymer-lipid particles (PLPs), preserving aspects of the native membrane context compatible with downstream biophysical techniques. Single-particle cryo-electron microscopy (cryo-EM) has become a principal method for MP structure determination. Here, we review progress in the development and application of extraction polymers for MP structural biology, highlighting studies that demonstrate how polymer chemistry can influence protein behaviour, lipid retention and conformational sampling sometimes revealing biologically relevant states unseen when using detergents and/or systems such as nanodiscs. Finally, we discuss current limitations, outlining future directions towards rational polymer design to advance MP structural and mechanistic understanding while supporting improved drug discovery.
| Original language | English |
|---|---|
| Article number | 103331 |
| Number of pages | 9 |
| Journal | Current Opinion in Structural Biology |
| Volume | 100 |
| Early online date | 20 Jul 2026 |
| DOIs | |
| Publication status | E-pub ahead of print - 20 Jul 2026 |
Bibliographical note
Copyright © 2026 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/).Funding
The Aston Institute for Membrane Excellence (AIME) is funded by UKRI’s Research England as part of their Expanding Excellence in England (E3) fund.
| Funders |
|---|
| UK Research and Innovation |
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