Evidence map›Paper›PMID 41436486›Full record

ArticleScientific reports2025

The solute-binding proteins DppA1-5 of Pseudomonas aeruginosa have distinct substrate profiles.

Konstantin Plöchl, Thomas Böttcher

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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
–field-weighted citation impact
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.

  1. 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

2 authors.

Konstantin PlöchlFaculty of Chemistry, Institute of Biological Chemistry & Centre for Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria.
Thomas BöttcherFaculty of Chemistry, Institute of Biological Chemistry & Centre for Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria. thomas.boettcher@univie.ac.at.

Funding

Austrian Science Fund doi.org/10.55776/COE7H2020 European Research Council ERC Consolidator Grant 865849-CAPSID
6 · The paper itself

Abstract

Pseudomonas aeruginosa is an opportunistic pathogen with high antibiotic resistance that infects immunocompromised patients. Its survival in diverse environments relies on nutrient uptake systems such as the dipeptide permease (Dpp), an ATP-binding cassette transporter that imports di- and tripeptides. Unlike other bacteria, whose Dpp includes a single solute-binding protein that binds substrates in the periplasm, P. aeruginosa encodes five paralogs (DppA1-5), the functional significance of which remains unclear. Here, we systematically profile the ligand specificities of all five DppA proteins using Differential Scanning Fluorimetry with a library of 281 di- and tripeptides. We find that DppA1 and DppA3 preferentially bind dipeptides, whereas DppA2 and DppA4 favor tripeptides. DppA5 shows no detectable binding, suggesting a divergent function. Ligand binding is highly structure-sensitive and distinct across DppA paralogs. A comparative reanalysis of published nutrient utilization data for dppA1-5 suggests that previous studies underestimated this functional specialization. In contrast, our findings indicate that P. aeruginosa encodes multiple DppA paralogs to expand Dpp substrate scope and enhance nutrient acquisition. This work provides a foundation for further exploration of the Dpp in bacterial signaling and its exploitation for drug delivery via Trojan Horse antimicrobials.

Indexed as

Bacterial ProteinsMembrane Transport ProteinsPseudomonas aeruginosaDipeptidesLigandsProtein BindingSubstrate SpecificityBacterial ProteinsDipeptidesLigandsMembrane Transport Proteins

Identifiers

PMID41436486
PMCPMC12728205

What OpenQuestion holds

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Registered trials

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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.