Evidence map›Paper›PMID 24041905›Full record

ArticleAntimicrobial agents and chemotherapy2013

Tools for characterizing bacterial protein synthesis inhibitors.

Cédric Orelle, Skylar Carlson, Bindiya Kaushal, Mashal M Almutairi, Haipeng Liu, Anna Ochabowicz, Selwyn Quan, Van Cuong Pham, Catherine L Squires, Brian T Murphy and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

83 citing papers in PubMed, 130 citations in OpenAlex.

  1. Article
  2. Article
  3. Approaches for Studying Context Specificity of Translation Inhibitor Action.International journal of molecular sciences · 2026
    Review
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  6. The Spermidine Synthase Gene as a Reporter of Transcription Inhibition inInternational journal of molecular sciences · 2026
    Article
  7. Synergistic Action of Antimicrobial Peptides and Antibiotics.International journal of molecular sciences · 2026
    Review
  8. Article
  9. Negamycin: Nature's Forgotten Antibiotic.ACS infectious diseases · 2026
    Review
  10. An aryloxyphenol potentiates polymyxin against multidrug-resistantFrontiers in cellular and infection microbiology · 2026
    Article
  11. Characterization ofInternational journal of molecular sciences · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

23 more citing papers are in PubMed but not listed here.

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 3 institutions in 2 countries.

Cédric OrelleCenter for Pharmaceutical Biotechnology, University of Illinois, Chicago, Illinois, USA.
Skylar Carlson
Bindiya Kaushal
Mashal M Almutairi
Haipeng Liu
Anna Ochabowicz
Selwyn Quan
Van Cuong Pham
Catherine L Squires
Brian T Murphy
Alexander S Mankin
University of Illinois Chicago · USStanford University · USVietnam Academy of Science and Technology · VN

Funding

Molecular mechanisms of action of macrolide antibioticsR01GM106386 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MANKIN, ALEXANDER S, VAZQUEZ-LASLOP, NORA · 2013 to 2016
$1.2M
Inhibitors of Bacterial Protein Synthesis with Novel Modes of ActionR03DA035191 · NIDA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MANKIN, ALEXANDER S, ORELLE, CEDRIC · 2012 to 2013
$79k
NIDA NIH HHS R03 DA035191NIDA NIH HHS R03DA035191NIGMS NIH HHS R01 GM106386
6 · The paper itself

Abstract

Many antibiotics inhibit the growth of sensitive bacteria by interfering with ribosome function. However, discovery of new protein synthesis inhibitors is curbed by the lack of facile techniques capable of readily identifying antibiotic target sites and modes of action. Furthermore, the frequent rediscovery of known antibiotic scaffolds, especially in natural product extracts, is time-consuming and expensive and diverts resources that could be used toward the isolation of novel lead molecules. In order to avoid these pitfalls and improve the process of dereplication of chemically complex extracts, we designed a two-pronged approach for the characterization of inhibitors of protein synthesis (ChIPS) that is suitable for the rapid identification of the site and mode of action on the bacterial ribosome. First, we engineered antibiotic-hypersensitive Escherichia coli strains that contain only one rRNA operon. These strains are used for the rapid isolation of resistance mutants in which rRNA mutations identify the site of the antibiotic action. Second, we show that patterns of drug-induced ribosome stalling on mRNA, monitored by primer extension, can be used to elucidate the mode of antibiotic action. These analyses can be performed within a few days and provide a rapid and efficient approach for identifying the site and mode of action of translation inhibitors targeting the bacterial ribosome. Both techniques were validated using a bacterial strain whose culture extract, composed of unknown metabolites, exhibited protein synthesis inhibitory activity; we were able to rapidly detect the presence of the antibiotic chloramphenicol.

Indexed as

Gene Expression Regulation, BacterialAnti-Bacterial AgentsBase SequenceDNA PrimersDrug Resistance, BacterialEscherichia coliGenetic EngineeringMolecular Sequence DataMutationNucleic Acid ConformationProtein BiosynthesisProtein Synthesis InhibitorsRibosomesrRNA OperonSubcellular FractionsAnti-Bacterial AgentsDNA PrimersProtein Synthesis Inhibitors

Identifiers

PMID24041905
PMCPMC3837844
OpenAlexW2125776589

What OpenQuestion holds

Textmetadata
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.