Evidence map›Paper›PMID 33148162›Full record

ArticleBMC molecular and cell biology2020

Polymerization of Bacillus subtilis MreB on a lipid membrane reveals lateral co-polymerization of MreB paralogs and strong effects of cations on filament formation.

Simon Dersch, Christian Reimold, Joshua Stoll, Hannes Breddermann, Thomas Heimerl, Hervé Joel Defeu Soufo, Peter L Graumann

Open access · goldAbstract read
In one paragraph

Article in BMC molecular and cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Simon DerschCentre for Synthetic Microbiology (SYNMIKRO) Hans-Meerwein Strasse 6, Philipps-Universität Marburg, 35032, Marburg, Germany.
Christian ReimoldCentre for Synthetic Microbiology (SYNMIKRO) Hans-Meerwein Strasse 6, Philipps-Universität Marburg, 35032, Marburg, Germany.
Joshua StollCentre for Synthetic Microbiology (SYNMIKRO) Hans-Meerwein Strasse 6, Philipps-Universität Marburg, 35032, Marburg, Germany.
Hannes BreddermannInstitut für Genetik, Zülpicherstr. 47a, 50674, Köln, Germany.
Thomas HeimerlCentre for Synthetic Microbiology (SYNMIKRO) Hans-Meerwein Strasse 6, Philipps-Universität Marburg, 35032, Marburg, Germany.
Hervé Joel Defeu SoufoDepartment of Microsystems Engineering - IMTEK, University of Freiburg, 79110, Freiburg, Germany.
Peter L GraumannCentre for Synthetic Microbiology (SYNMIKRO) Hans-Meerwein Strasse 6, Philipps-Universität Marburg, 35032, Marburg, Germany. graumanp@uni-marburg.de.ORCID http://orcid.org/0000-0002-8033-5171
Philipps University of Marburg · DEUniversity of Freiburg · DE

Funding

Deutsche Forschungsgemeinschaft GR1670/23-1
6 · The paper itself

Abstract

backgroundMreB is a bacterial ortholog of actin and forms mobile filaments underneath the cell membrane, perpendicular to the long axis of the cell, which play a crucial role for cell shape maintenance. We wished to visualize Bacillus subtilis MreB in vitro and therefore established a protocol to obtain monomeric protein, which could be polymerized on a planar membrane system, or associated with large membrane vesicles.

resultsUsing a planar membrane system and electron microscopy, we show that Bacillus subtilis MreB forms bundles of filaments, which can branch and fuse, with an average width of 70 nm. Fluorescence microscopy of non-polymerized YFP-MreB, CFP-Mbl and mCherry-MreBH proteins showed uniform binding to the membrane, suggesting that 2D diffusion along the membrane could facilitate filament formation. After addition of divalent magnesium and calcium ions, all three proteins formed highly disordered sheets of filaments that could split up or merge, such that at high protein concentration, MreB and its paralogs generated a network of filaments extending away from the membrane. Filament formation was positively affected by divalent ions and negatively by monovalent ions. YFP-MreB or CFP-Mbl also formed filaments between two adjacent membranes, which frequently has a curved appearance. New MreB, Mbl or MreBH monomers could add to the lateral side of preexisting filaments, and MreB paralogs co-polymerized, indicating direct lateral interaction between MreB paralogs.

conclusionsOur data show that B. subtilis MreB paralogs do not easily form ordered filaments in vitro, possibly due to extensive lateral contacts, but can co-polymerise. Monomeric MreB, Mbl and MreBH uniformly bind to a membrane, and form irregular and frequently split up filamentous structures, facilitated by the addition of divalent ions, and counteracted by monovalent ions, suggesting that intracellular potassium levels may be one important factor to counteract extensive filament formation and filament splitting in vivo.

Indexed as

Actin CytoskeletonBacillus subtilisBacterial ProteinsCalciumCationsDynamic Light ScatteringEscherichia coliLipid BilayersLuminescent ProteinsMagnesiumMembrane LipidsMembranes, ArtificialMicroscopy, ElectronPolymerizationPolymersRecombinant ProteinsBacterial ProteinsCalciumCationsLipid BilayersLuminescent ProteinsMagnesiumMembrane LipidsMembranes, ArtificialPolymersRecombinant Proteins

Identifiers

PMID33148162
PMCPMC7641798
OpenAlexW3096117831

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.