Evidence map›Paper›PMID 41553449›Full record

ArticleJournal of plant research2026

Advanced lipidomic techniques for high-throughput profiling of complex sphingolipids in plant tissues.

Toshiki Ishikawa

Abstract read
In one paragraph

Article in Journal of plant research, 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

1 author.

Toshiki IshikawaGraduate School of Science and Engineering, Saitama University, 255 Shimo-Okubo, Sakura-Ku, Saitama, Japan. toishika@mail.saitama-u.ac.jp.ORCID http://orcid.org/0000-0001-8083-6542

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingolipids are essential membrane components that regulate various cellular functions by forming ordered domains. The structural core of sphingolipids comprises a long-chain sphingoid base and its N-acylated ceramide, modified with diverse head groups to form complex sphingolipids. In plants, sphingolipid structures exhibit unique structural diversity in both the ceramide moiety and head group. The complicated sphingolipid structures suggest unique functions, but complicate lipidomic studies. A new methodology was established for simple sample preparation and targeted mass spectrometry, to advance high-throughput techniques for plant sphingolipidomics. A single-tube extraction protocol, consisting of the sequential procedures of enzyme inactivation, alkaline saponification and acidic 1-butanol phase partitioning, was optimized to enable rapid (~ 2.5 h) preparation of all sphingolipid classes with improved recovery. Over 900 molecular species from a theoretical plant sphingolipidome library were separated via reverse-phase liquid chromatography and quantified in a single run using scheduled monitoring of targeted mass spectrometry. This method enables large-scale profiling of the natural distribution of sphingolipids across diverse plant materials.

Indexed as

LipidomicsPlantsSphingolipidsHigh-Throughput Screening AssaysLiquid Chromatography-Mass SpectrometryMass SpectrometryTandem Mass SpectrometrySphingolipidsGlycosylinositol phosphoceramide (GIPC)LC–MS/MSLipidomicsScheduled multiple reaction monitoring (MRM)Sphingolipids

Identifiers

PMID41553449
PMCPMC12992377

What Socratic 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 Socratic graph.