Evidence map›Paper›PMID 25655041›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2015

Structural and functional implications of the interaction between macrolide antibiotics and bile acids.

Simon Glanzer, Sergio A Pulido, Sarah Tutz, Gabriel E Wagner, Manfred Kriechbaum, Nina Gubensäk, Jovana Trifunovic, Markus Dorn, Walter M F Fabian, Predrag Novak and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.0field-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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  7. Review
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  12. Investigating Protein-Ligand Interactions by Solution Nuclear Magnetic Resonance Spectroscopy.Chemphyschem : a European journal of chemical physics and physical chemistry · 2018
    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

12 authors at 4 institutions in 3 countries.

Simon GlanzerInstitute of Chemistry, University of Graz (Austria).
Sergio A Pulido
Sarah Tutz
Gabriel E Wagner
Manfred Kriechbaum
Nina Gubensäk
Jovana Trifunovic
Markus Dorn
Walter M F Fabian
Predrag Novak
Joachim Reidl
Klaus Zangger
University of Graz · ATGraz University of Technology · ATUniversity of Novi Sad · RSUniversity of Zagreb · HR

Funding

Austrian Science Fund FWF P 25880
6 · The paper itself

Abstract

Macrolide antibiotics, such as azithromycin and erythromycin, are in widespread use for the treatment of bacterial infections. Macrolides are taken up and excreted mainly by bile. Additionally, they have been implicated in biliary system diseases and to modify the excretion of other drugs through bile. Despite mounting evidence for the interplay between macrolide antibiotics and bile acids, the molecular details of this interaction remain unknown. Herein, we show by NMR measurements that macrolides directly bind to bile acid micelles. The topology of this interaction has been determined by solvent paramagnetic relaxation enhancements (solvent PREs). The macrolides were found to be bound close to the surface of the micelle. Increasing hydrophobicity of both the macrolide and the bile acid strengthen this interaction. Both bile acid and macrolide molecules show similar solvent PREs across their whole structures, indicating that there are no preferred orientations of them in the bile micelle aggregates. The binding to bile aggregates does not impede macrolide antibiotics from targeting bacteria. In fact, the toxicity of azithromycin towards enterotoxic E. coli (ETEC) is even slightly increased in the presence of bile, as was shown by effective concentration (EC50 ) values.

Indexed as

Anti-Bacterial AgentsBile Acids and SaltsMacrolidesMolecular StructureAnti-Bacterial AgentsBile Acids and SaltsMacrolidesazithromycinbile acidsdiffusion ordered spectroscopy (DOSY)macrolide antibioticsmicellesNMR spectroscopy

Identifiers

PMID25655041
PMCPMC4471570
OpenAlexW2066458302

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.