<scp>RePol</scp> : A high‐throughput screen for optimizing membrane protein solubilization and purification using polymers

Extraction and purification of membrane proteins has for a long time represented a significant challenge. Polymer-based extraction methods, like those using styrene maleic acid co-polymers have provided a fertile approach to generate samples that include the local lipid environment surrounding the protein. However, the wide variety of different polymers now available provides a challenge to identify the optimal solution. In this study we develop and demonstrate a novel high-throughput screening approach for rapid optimization of polymer solubilization agents and chromatography resins for membrane protein purification. Using this approach, we explore whether there are standard conditions that perform well for a range of membrane protein morphologies, sources and functions. These data show that no such standard conditions exist for either polymer solubilization agent or chromatography resin and that some combinations are rarely suitable for membrane protein purifications under these conditions, such as the use of TALON resin at a pH of 7.5 or SMALP300 in the Synthetic Nanodisc Screening Kit MINI kit. Instead, the use of the screening approach developed in this work is the best route to an optimal membrane protein preparation protocol.

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Publication Details

Journal
Protein Science
Published
2025-12-22
DOI
https://doi.org/10.1002/pro.70407
Primary Topic
Lipid Membrane Structure and Behavior
Type
article
Field-Weighted Citation Impact
0.00

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article

RePol : A high‐throughput screen for optimizing membrane protein solubilization and purification using polymers

David I. Roper, A. Evans, Philip M. Ireland, Alice J. Rothnie et al.
Protein Science
Lipid Membrane Structure and Behavior
article

RePol : A high‐throughput screen for optimizing membrane protein solubilization and purification using polymers

David I. Roper, A. Evans, Philip M. Ireland, Alice J. Rothnie, Naomi Pollock, Pooja Sridhar, Tim R. Dafforn, Bethan Kelly
article en

Abstract

Extraction and purification of membrane proteins has for a long time represented a significant challenge. Polymer-based extraction methods, like those using styrene maleic acid co-polymers have provided a fertile approach to generate samples that include the local lipid environment surrounding the protein. However, the wide variety of different polymers now available provides a challenge to identify the optimal solution. In this study we develop and demonstrate a novel high-throughput screening approach for rapid optimization of polymer solubilization agents and chromatography resins for membrane protein purification. Using this approach, we explore whether there are standard conditions that perform well for a range of membrane protein morphologies, sources and functions. These data show that no such standard conditions exist for either polymer solubilization agent or chromatography resin and that some combinations are rarely suitable for membrane protein purifications under these conditions, such as the use of TALON resin at a pH of 7.5 or SMALP300 in the Synthetic Nanodisc Screening Kit MINI kit. Instead, the use of the screening approach developed in this work is the best route to an optimal membrane protein preparation protocol.

Protein ScienceVol. 35(1)
Defence Science and Technology Laboratory (GB), Aston University (GB), University of Warwick (GB), University of Birmingham (GB)
UK Research and Innovation, Directorate for Biological Sciences, Research England
Openalex Percentile: Top 37%
Lipid Membrane Structure and Behavior
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<scp>RePol</scp> : A high‐throughput screen for optimizing membrane protein solubilization and purification using polymers — David I. Roper, A. Evans, et al. · Protein Science (2025) | TGRS Research Map | TGRS