Evidence map›Paper›PMID 29461535›Full record

ArticleNature chemistry2018

Direct observation of the influence of cardiolipin and antibiotics on lipid II binding to MurJ.

Jani Reddy Bolla, Joshua B Sauer, Di Wu, Shahid Mehmood, Timothy M Allison, Carol V Robinson

Open access · greenAbstract read
In one paragraph

Article in Nature chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

48 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. Journal of bacteriology · 2025
    Article
  3. Article
  4. Lipopeptide antibiotics disrupt interactions of undecaprenyl phosphate with UptA.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Emergence of mass spectrometry detergents for membrane proteomics.Analytical and bioanalytical chemistry · 2023
    Review
  13. Review
  14. Shapeshifting bullvalene-linked vancomycin dimers as effective antibiotics against multidrug-resistant gram-positive bacteria.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Structure and Mechanism of the Lipid Flippase MurJ.Annual review of biochemistry · 2022
    Review
  20. 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

6 authors at 1 institution in 1 country.

Jani Reddy BollaDepartment of Chemistry, University of Oxford, South Parks Road, Oxford, OX1 3QZ, UK.ORCID 0000-0003-4346-182X
Joshua B SauerDepartment of Chemistry, University of Oxford, South Parks Road, Oxford, OX1 3QZ, UK.
Di WuDepartment of Chemistry, University of Oxford, South Parks Road, Oxford, OX1 3QZ, UK.
Shahid MehmoodDepartment of Chemistry, University of Oxford, South Parks Road, Oxford, OX1 3QZ, UK.
Timothy M AllisonDepartment of Chemistry, University of Oxford, South Parks Road, Oxford, OX1 3QZ, UK.
Carol V RobinsonDepartment of Chemistry, University of Oxford, South Parks Road, Oxford, OX1 3QZ, UK.
University of Oxford · GB

Funding

European Research Council 641317Medical Research Council MR/N020413/1Wellcome Trust 104633
6 · The paper itself

Abstract

Translocation of lipid II across the cytoplasmic membrane is essential in peptidoglycan biogenesis. Although most steps are understood, identifying the lipid II flippase has yielded conflicting results, and the lipid II binding properties of two candidate flippases-MurJ and FtsW-remain largely unknown. Here we apply native mass spectrometry to both proteins and characterize lipid II binding. We observed lower levels of lipid II binding to FtsW compared to MurJ, consistent with MurJ having a higher affinity. Site-directed mutagenesis of MurJ suggests that mutations at A29 and D269 attenuate lipid II binding to MurJ, whereas chemical modification of A29 eliminates binding. The antibiotic ramoplanin dissociates lipid II from MurJ, whereas vancomycin binds to form a stable complex with MurJ:lipid II. Furthermore, we reveal cardiolipins associate with MurJ but not FtsW, and exogenous cardiolipins reduce lipid II binding to MurJ. These observations provide insights into determinants of lipid II binding to MurJ and suggest roles for endogenous lipids in regulating substrate binding.

Indexed as

Anti-Bacterial AgentsBacterial ProteinsBinding SitesCardiolipinsDepsipeptidesEscherichia coli ProteinsMass SpectrometryMembrane ProteinsMutagenesis, Site-DirectedPhospholipid Transfer ProteinsUridine Diphosphate N-Acetylmuramic AcidAnti-Bacterial AgentsBacterial ProteinsCardiolipinsDepsipeptidesEscherichia coli ProteinsFtsW protein, BacteriaMembrane Proteinsmuramyl-NAc-(pentapeptide)pyrophosphoryl-undecaprenolMurJ protein, E coliPhospholipid Transfer ProteinsramoplaninUridine Diphosphate N-Acetylmuramic Acid

Identifiers

PMID29461535
PMCPMC5912511
OpenAlexW2782885942

What OpenQuestion holds

Textmetadata
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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.