Evidence map›Paper›PMID 41720527›Full record

ArticleMethods in enzymology2026

High-resolution sphingolipid analysis in vitro using LC-qToF MS.

Shweta Chitkara, G Ekin Atilla-Gokcumen

Abstract read
In one paragraph

Article in Methods in enzymology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Shweta ChitkaraDepartment of Chemistry, University at Buffalo, The State University of New York, Buffalo, NY, United States.
G Ekin Atilla-GokcumenDepartment of Chemistry, University at Buffalo, The State University of New York, Buffalo, NY, United States. Electronic address: ekinatil@buffalo.edu.

Funding

Mechanisms and consequences of lipid accumulations in necroptosisR35GM156195 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Gunes Ekin Atilla-Gokcumen · 2025 to 2026
$796k
NIGMS NIH HHS R35 GM156195
6 · The paper itself

Abstract

The complexity of the sphingolipidome, characterized by variations in chain length, saturation, and headgroup composition, makes it essential to develop analytical strategies capable of high sensitivity and structural precision. Traditional biochemical methods lack the resolution to discriminate among closely related species, underscoring the transformative role of liquid chromatography-mass spectrometry (LC-MS) in sphingolipidomics. LC-MS provides unparalleled capabilities for sphingolipid analysis, combining chromatographic separation with high-resolution mass detection to achieve both qualitative and quantitative accuracy. In particular, liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (LC-qToF MS) has emerged as a powerful platform, offering mass accuracy, broad dynamic range, and rapid acquisition rates. These features enable confident identification of isobaric and structurally related sphingolipids, which is essential for understanding their roles in cellular physiology and pathology. This chapter focuses on an optimized LC-qToF MS method tailored for sphingolipid profiling in cultured mammalian cells. By focusing on the analytical strengths of LC-MS, the approach provides a robust foundation for dissecting sphingolipid metabolism and its dysregulation in cellular processes.

Indexed as

LipidomicsLiquid Chromatography-Mass SpectrometrySphingolipidsAnimalsChromatography, LiquidHumansMass SpectrometrySphingolipidsCeramidesLC-MSLC-qToF MSSphingolipids

Identifiers

PMID41720527
PMCPMC13006889

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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.