Evidence map›Paper›PMID 36414253›Full record

ArticleACS chemical biology2022

Coupling Novel Probes with Molecular Localization Microscopy Reveals Cell Wall Homeostatic Mechanisms in

Victoria A Lund, Haneesh Gangotra, Zhen Zhao, Joshua A F Sutton, Katarzyna Wacnik, Kristen DeMeester, Hai Liang, Cintia Santiago, Catherine Leimkuhler Grimes, Simon Jones and 1 more

Open access · hybridAbstract read
In one paragraph

Article in ACS chemical biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. ACS infectious diseases · 2026
    Article
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

11 authors at 2 institutions in 2 countries.

Victoria A LundSchool of Biosciences, University of Sheffield, Sheffield S10 2TN, United Kingdom.
Haneesh GangotraThe Florey Institute for Host-Pathogen Interactions, University of Sheffield, Sheffield S10 2TN, United Kingdom.
Zhen ZhaoThe Florey Institute for Host-Pathogen Interactions, University of Sheffield, Sheffield S10 2TN, United Kingdom.
Joshua A F SuttonSchool of Biosciences, University of Sheffield, Sheffield S10 2TN, United Kingdom.
Katarzyna WacnikSchool of Biosciences, University of Sheffield, Sheffield S10 2TN, United Kingdom.
Kristen DeMeesterDepartment of Chemistry and Biochemistry and Department of Biological Sciences, University of Delaware, Newark, Delaware 19716, United States.
Hai LiangDepartment of Chemistry and Biochemistry and Department of Biological Sciences, University of Delaware, Newark, Delaware 19716, United States.
Cintia SantiagoDepartment of Chemistry and Biochemistry and Department of Biological Sciences, University of Delaware, Newark, Delaware 19716, United States.ORCID 0000-0001-8579-7968
Catherine Leimkuhler GrimesDepartment of Chemistry and Biochemistry and Department of Biological Sciences, University of Delaware, Newark, Delaware 19716, United States.ORCID 0000-0002-0586-2879
Simon JonesThe Florey Institute for Host-Pathogen Interactions, University of Sheffield, Sheffield S10 2TN, United Kingdom.ORCID 0000-0001-8043-7998
Simon J FosterSchool of Biosciences, University of Sheffield, Sheffield S10 2TN, United Kingdom.ORCID 0000-0001-7432-7805
University of Sheffield · GBUniversity of Delaware · US

Funding

Chemistry-Biology Interface Predoctoral Training Grant 2024-2029T32GM133395 · NIGMS · UNIVERSITY OF DELAWARE · PI Catherine Leimkuhler Grimes · 2019 to 2026
$3.7M
Metabolic carbohydrate cell wall probes for bacterial structure and immune recognition studiesU01CA221230 · NCI · UNIVERSITY OF DELAWARE · PI GRIMES, CATHERINE LEIMKUHLER · 2017 to 2019
$1.1M
Medical Research Council MR/N002679/1NCI NIH HHS U01 CA221230NIGMS NIH HHS T32 GM133395Wellcome Trust 212197/Z/19/Z
6 · The paper itself

Abstract

Bacterial cell wall peptidoglycan is essential for viability, and its synthesis is targeted by antibiotics, including penicillin. To determine how peptidoglycan homeostasis controls cell architecture, growth, and division, we have developed novel labeling approaches. These are compatible with super-resolution fluorescence microscopy to examine peptidoglycan synthesis, hydrolysis, and the localization of the enzymes required for its biosynthesis (penicillin binding proteins (PBPs)). Synthesis of a cephalosporin-based fluorescent probe revealed a pattern of PBPs at the septum during division, supporting a model of dispersed peptidoglycan synthesis. Metabolic and hydroxylamine-based probes respectively enabled the synthesis of glycan strands and associated reducing termini of the peptidoglycan to be mapped. Foci and arcs of reducing termini appear as a result of both synthesis of glycan strands and glucosaminidase activity of the major peptidoglycan hydrolase, SagB. Our studies provide molecular level details of how essential peptidoglycan dynamics are controlled during growth and division.

Indexed as

Staphylococcal InfectionsStaphylococcus aureusBacterial ProteinsCell WallHomeostasisHumansMicroscopy, FluorescencePenicillin-Binding ProteinsPeptidoglycanBacterial ProteinsPenicillin-Binding ProteinsPeptidoglycan

Identifiers

PMID36414253
PMCPMC9764285
OpenAlexW4309672915

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.