Evidence map›Paper›PMID 41008622›Full record

ReviewBiomolecules2025

Coming Clean and Avoiding Bubble Trouble-Using Detergents Wisely in the Purification of Membrane Proteins for Cryo-EM Studies.

Bowen Chen, Peter Harrison, Vasileios Kargas, Naomi Pollock, Robert C Ford, Stephen M Prince, Richard F Collins

Abstract readReview
In one paragraph

Review in Biomolecules, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Bowen ChenFaculty of Biology, Medicine and Health, Smith Building, The University of Manchester, Dover Street, Manchester M13 9PL, UK.
Peter HarrisonThe Membrane Protein Laboratory and the Electron Bio-Imaging Centre (eBIC), Diamond Light Source, Harwell Science & Innovation Campus, Oxford OX11 0DE, UK.
Vasileios KargasCambridge Institute for Medical Research, University of Cambridge, Cambridge Biomedical Campus, The Keith Peters Building, Hills Road, Cambridge CB2 0XY, UK.ORCID 0000-0001-8588-7285
Naomi PollockHealth & Life Sciences, Aston University, Aston St, Birmingham B4 7ET, UK.
Robert C FordFaculty of Biology, Medicine and Health, Smith Building, The University of Manchester, Dover Street, Manchester M13 9PL, UK.ORCID 0000-0002-0958-1505
Stephen M PrinceFaculty of Biology, Medicine and Health, Smith Building, The University of Manchester, Dover Street, Manchester M13 9PL, UK.ORCID 0000-0003-0929-0254
Richard F CollinsFaculty of Biology, Medicine and Health, Smith Building, The University of Manchester, Dover Street, Manchester M13 9PL, UK.

Funding

Biotechnology and Biological Sciences Research Council ALERT 2020 BB/T017643/1Diamond Light Source NR-27436 & NT-33941Science and Technology Facilities Council BAG 29255 & 36408Wellcome TrustWellcome Trust 223727/Z/21/Z
6 · The paper itself

Abstract

Detergent solubilisation remains the most commonly used but potentially problematic method to extract membrane proteins from lipid bilayers for Cryo-EM studies. Although recent advances have introduced excellent alternatives-such as amphipols, nanodiscs and SMALPs-the use of detergents is often necessary for intermediate steps. In this paper, we share our experiences working with detergent-solubilised samples within the modern Cryo-EM structural pipeline from the perspective of an EM specialist. Our aim is to inform novice users about potential challenges they may encounter. Drawing on specific examples from a variety of biological membrane systems, including Magnesium channels, lipopolysaccharide biosynthesis, and the human major facilitator superfamily transporters, we describe how the intrinsic properties of detergent-extracted samples can affect protein purification, Cryo-EM grid preparation (including the formation of vitreous ice) and the reconstitution of proteins into micelles. We also discuss how these unique characteristics can impact different stages of structural analysis and lead to complications in single-particle averaging software analysis. For each case, we present our insights into the underlying causes and suggest possible mitigations or alternative approaches.

Indexed as

Cryoelectron MicroscopyDetergentsMembrane ProteinsHumansLipid BilayersMicellesDetergentsLipid BilayersMembrane ProteinsMicellesCorA Magnesium channel structurecryo electron microscopyCryo-EM grid preparationdetergent purificationmembrane proteinsmembrane protein structureoligomeric complexessingle particle averagingtransmembrane helicesWzz lipopolysaccharide biosynthesis

Identifiers

PMID41008622
PMCPMC12466997

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.