Evidence map›Paper›PMID 40167996›Full record

ArticleAnalytical chemistry2025

Rapid MALDI-MS/MS-Based Profiling of Lipid A Species from Gram-Negative Bacteria Utilizing Trapped Ion Mobility Spectrometry and mzmine.

Edward Rudt, Matti Froning, Steffen Heuckeroth, Lucas Ortmann, Julia Diemand, Linus Hörnschemeyer, Alexander Pleger, Max Vinzelberg, Robin Schmid, Tomáš Pluskal and 3 more

Abstract read
In one paragraph

Article in Analytical chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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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

13 authors.

Edward RudtInstitute of Inorganic and Analytical Chemistry, University of Münster, Corrensstraße 48, D-48149 Münster, Germany.ORCID 0000-0003-4351-3212
Matti FroningInstitute of Inorganic and Analytical Chemistry, University of Münster, Corrensstraße 48, D-48149 Münster, Germany.
Steffen Heuckerothmzio GmbH, Altenwall 26, D-28195 Bremen, Germany.ORCID 0000-0002-4928-2526
Lucas OrtmannInstitute of Inorganic and Analytical Chemistry, University of Münster, Corrensstraße 48, D-48149 Münster, Germany.ORCID 0009-0002-4929-2078
Julia DiemandInstitute of Inorganic and Analytical Chemistry, University of Münster, Corrensstraße 48, D-48149 Münster, Germany.
Linus HörnschemeyerInstitute of Inorganic and Analytical Chemistry, University of Münster, Corrensstraße 48, D-48149 Münster, Germany.
Alexander PlegerInstitute of Inorganic and Analytical Chemistry, University of Münster, Corrensstraße 48, D-48149 Münster, Germany.
Max VinzelbergInstitute of Inorganic and Analytical Chemistry, University of Münster, Corrensstraße 48, D-48149 Münster, Germany.
Robin Schmidmzio GmbH, Altenwall 26, D-28195 Bremen, Germany.
Tomáš PluskalInstitute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo náméstí 542/2, 160 00 Prague, Czech Republic.ORCID 0000-0002-6940-3006
Ulrich DobrindtInstitute of Hygiene, University of Münster, Mendelstraße 7, D-48149 Münster, Germany.
Heiko HayenInstitute of Inorganic and Analytical Chemistry, University of Münster, Corrensstraße 48, D-48149 Münster, Germany.ORCID 0000-0002-4074-8545
Ansgar Korfmzio GmbH, Altenwall 26, D-28195 Bremen, Germany.ORCID 0000-0002-2769-2460

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipid A, a crucial component of lipopolysaccharides (LPS), plays a pivotal role in the pathogenesis of Gram-negative bacteria. Lipid A patterns are recognized by mammals and can induce immunostimulatory effects. However, the outcome of the interaction is highly dependent on the chemical composition of individual lipid A species. The diversity of potential fatty acyl and polar headgroup combinations in this complex saccharolipid presents a significant analytical challenge. Current mass spectrometry (MS)-based lipid A methods are focused on either direct matrix-assisted laser desorption/ionization (MALDI)-MS screening or comprehensive structural elucidation by tandem mass spectrometry (MS/MS) hyphenated with separation techniques. In this study, we developed an alternative workflow for rapid lipid A profiling covering the entire analysis pipeline from sample preparation to data analysis. This workflow is based on microextraction and subsequent MALDI-MS/MS analysis of uropathogenic

Indexed as

Gram-Negative BacteriaIon Mobility SpectrometryLipid ASpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationUropathogenic Escherichia coliTandem Mass SpectrometryLipid A

Identifiers

PMID40167996
PMCPMC12004357

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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.