Evidence map›Paper›PMID 30679312›Full record

ArticleThe Journal of biological chemistry2019

Universal fluorescent sensors of high-affinity iron transport, applied to ESKAPE pathogens.

Somnath Chakravorty, Yan Shipelskiy, Ashish Kumar, Aritri Majumdar, Taihao Yang, Brittany L Nairn, Salete M Newton, Phillip E Klebba

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Siderophore-mediated iron acquisition byJournal of bacteriology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Conformational rearrangements in the N-domain ofThe Journal of biological chemistry · 2020
    Article
  8. Considerations and Caveats in Combating ESKAPE Pathogens against Nosocomial Infections.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    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

8 authors at 2 institutions in 1 country.

Somnath ChakravortyFrom the Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, Kansas 66506 and.
Yan ShipelskiyFrom the Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, Kansas 66506 and.
Ashish KumarFrom the Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, Kansas 66506 and.
Aritri MajumdarFrom the Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, Kansas 66506 and.
Taihao YangFrom the Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, Kansas 66506 and.
Brittany L Nairnthe Department of Biological Sciences, Bethel University, St. Paul, Minnesota 55112.
Salete M NewtonFrom the Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, Kansas 66506 and.ORCID 0000-0002-8327-8424
Phillip E KlebbaFrom the Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, Kansas 66506 and peklebba@ksu.edu.
Kansas State University · USBethel University · US

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SUSAN J. BROWN · 2012 to 2026
$63.0M
High-throughput fluorescence screening for inhibitors of TonB-dependent iron transportR21AI115187 · NIAID · KANSAS STATE UNIVERSITY · PI KLEBBA, PHILLIP E · 2015 to 2016
$388k
NIAID NIH HHS R21 AI115187NIGMS NIH HHS P20 GM103418
6 · The paper itself

Abstract

Sensitive assays of biochemical specificity, affinity, and capacity are valuable both for basic research and drug discovery. We created fluorescent sensors that monitor high-affinity binding reactions and used them to study iron acquisition by ESKAPE bacteria, which are frequently responsible for antibiotic-resistant infections. By introducing site-directed Cys residues in bacterial iron transporters and modifying them with maleimide fluorophores, we generated living cells or purified proteins that bind but do not transport target compounds. These constructs sensitively detected ligand concentrations in solution, enabling accurate, real-time spectroscopic analysis of membrane transport by other cells. We assessed the efficacy of these "fluorescent decoy" (FD) sensors by characterizing active iron transport in the ESKAPE bacteria. The FD sensors monitored uptake of both ferric siderophores and hemin by the pathogens. An FD sensor for a particular ligand was universally effective in observing the uptake of that compound by all organisms we tested. We adapted the FD sensors to microtiter format, where they allow high-throughput screens for chemicals that block iron uptake, without genetic manipulations of the virulent target organisms. Hence, screening assays with FD sensors facilitate studies of mechanistic biochemistry, as well as discovery of chemicals that inhibit prokaryotic membrane transport. With appropriate design, FD sensors are potentially applicable to any pro- or eukaryotic high-affinity ligand transport process.

Indexed as

Biosensing TechniquesBacteriaBiological TransportFluorescenceHemeHigh-Throughput Screening AssaysIronSpectrometry, FluorescenceHemeIronESKAPE pathogenfluorescencehemeironligand-binding proteinmembrane transportpathogenesissiderophorespectroscopy

Identifiers

PMID30679312
PMCPMC6433069
OpenAlexW2912738373

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.