Evidence map›Paper›PMID 40617869›Full record

ArticleNature communications2025

A porin-like protein used by bacterial predators defines a wider lipid-trapping superfamily.

Rebecca J Parr, Yoann G Santin, Giedrė Ratkevičiūte, Simon G Caulton, Paul Radford, Dominik Gurvič, Matthew Jenkins, Matthew T Doyle, Liam Mead, Augustinas Silale and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

16 authors.

Rebecca J ParrSchool of Biosciences, University of Birmingham, Birmingham, UK.
Yoann G Santin *de Duve Institute, UCLouvain, 75 Avenue Hippocrate 75, bte B1.75.08, Brussels, Belgium.
Giedrė Ratkevičiūte *School of Biosciences, University of Birmingham, Birmingham, UK.
Simon G CaultonSchool of Biosciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0001-7509-9728
Paul RadfordSchool of Life Sciences, Nottingham University, Medical School, Queen's Medical Centre, Nottingham, UK.ORCID http://orcid.org/0000-0002-0314-0346
Dominik GurvičSchool of Life Sciences & Department of Chemistry, Gibbet Hill Campus, The University of Warwick, Coventry, UK.
Matthew JenkinsSchool of Biosciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0009-0006-4119-3509
Matthew T DoyleSchool of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Darlington, NSW, Australia.ORCID http://orcid.org/0000-0002-1876-1209
Liam MeadSchool of Biosciences, University of Birmingham, Birmingham, UK.
Augustinas SilaleBiosciences Institute, Faculty of Medical Sciences, Newcastle University, Framlington Place, Newcastle upon Tyne, UK.ORCID http://orcid.org/0000-0003-3338-2087
Bert van den BergBiosciences Institute, Faculty of Medical Sciences, Newcastle University, Framlington Place, Newcastle upon Tyne, UK.ORCID http://orcid.org/0000-0003-1966-8804
Timothy J KnowlesSchool of Biosciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0002-6632-0985
R Elizabeth SockettSchool of Life Sciences, Nottingham University, Medical School, Queen's Medical Centre, Nottingham, UK.ORCID http://orcid.org/0000-0002-6271-2674
Phillip J StansfeldSchool of Life Sciences & Department of Chemistry, Gibbet Hill Campus, The University of Warwick, Coventry, UK.ORCID http://orcid.org/0000-0001-8800-7669
Géraldine Lalouxde Duve Institute, UCLouvain, 75 Avenue Hippocrate 75, bte B1.75.08, Brussels, Belgium. geraldine.laloux@uclouvain.be.ORCID http://orcid.org/0000-0003-3230-1679
Andrew L LoveringSchool of Biosciences, University of Birmingham, Birmingham, UK. a.lovering@bham.ac.uk.ORCID http://orcid.org/0000-0002-1856-7975

Funding

Wellcome Trust (Wellcome) 209437/Z/17/Z
6 · The paper itself

Abstract

Outer membrane proteins (OMPs) define the surface biology of Gram-negative bacteria, with roles in adhesion, transport, catalysis and signalling. Specifically, porin beta-barrels are common diffusion channels, predominantly monomeric/trimeric in nature. Here we show that the major OMP of the bacterial predator Bdellovibrio bacteriovorus, PopA, differs from this architecture, forming a pentameric porin-like superstructure. Our X-ray and cryo-EM structures reveal a bowl-shape composite outer β-wall, which houses a central chamber that encloses a section of the lipid bilayer. We demonstrate that PopA, reported to insert into prey inner membrane, causes defects when directed into Escherichia coli membranes. We discover widespread PopA homologues, including likely tetramers and hexamers, that retain the lipid chamber; a similar chamber is formed by an unrelated smaller closed-barrel family, implicating this as a general feature. Our work thus defines oligomeric OMP superfamilies, whose deviation from prior structures requires us to revisit existing membrane-interaction motifs and folding models.

Indexed as

Bacterial Outer Membrane ProteinsBdellovibrio bacteriovorusPorinsCryoelectron MicroscopyCrystallography, X-RayEscherichia coliLipid BilayersModels, MolecularBacterial Outer Membrane ProteinsLipid BilayersPorins

Identifiers

PMID40617869
PMCPMC12228718

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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.