Evidence map›Paper›PMID 26313480›Full record

ArticleNature protocols2015

Direct metabolomics for plant cells by live single-cell mass spectrometry.

Takashi Fujii, Shuichi Matsuda, Mónica Lorenzo Tejedor, Tsuyoshi Esaki, Iwao Sakane, Hajime Mizuno, Naohiro Tsuyama, Tsutomu Masujima

Abstract read
PubMed Publisher
In one paragraph

Article in Nature protocols, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing 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

82 citing papers in PubMed.

  1. Review
  2. Article
  3. Living single-cell metabolomicsChemical science · 2026
    Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Development of a highly efficient solubilization method for mass spectrometric analysis of phospholipids in living single cells.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2024
    Article
  19. bioRxiv : the preprint server for biology · 2024
    Article
  20. Review

22 more citing papers are in PubMed but not listed here.

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.

Takashi FujiiLaboratory for Molecular Medicine and Devices, Graduated School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Shuichi MatsudaLaboratory for Molecular Medicine and Devices, Graduated School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Mónica Lorenzo TejedorLaboratory for Molecular Medicine and Devices, Graduated School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Tsuyoshi EsakiLaboratory for Single Cell Mass Spectrometry, Quantitative Biology Center, RIKEN, Suita, Osaka, Japan.
Iwao SakaneLaboratory for Single Cell Mass Spectrometry, Quantitative Biology Center, RIKEN, Suita, Osaka, Japan.
Hajime MizunoLaboratory for Molecular Medicine and Devices, Graduated School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Naohiro TsuyamaLaboratory for Molecular Medicine and Devices, Graduated School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.ORCID http://orcid.org/0000-0002-4425-4526
Tsutomu MasujimaLaboratory for Molecular Medicine and Devices, Graduated School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Live single-cell mass spectrometry (live MS) provides a mass spectrum that shows thousands of metabolite peaks from a single live plant cell within minutes. By using an optical microscope, a cell is chosen for analysis and a metal-coated nanospray microcapillary tip is used to remove the cell's contents. After adding a microliter of ionization solvent to the opposite end of the tip, the trapped contents are directly fed into the mass spectrometer by applying a high voltage between the tip and the inlet port of the spectrometer to induce nanospray ionization. Proteins are not detected because of insufficient sensitivity. Metabolite peaks are identified by exact mass or tandem mass spectrometry (MS/MS) analysis, and isomers can be separated by combining live MS with ion-mobility separation. By using this approach, spectra can be acquired in 10 min. In combination with metabolic maps and/or molecular databases, the data can be annotated into metabolic pathways; the data analysis takes 30 min to 4 h, depending on the MS/MS data availability from databases. This method enables the analysis of a number of metabolites from a single cell with rapid sampling at sub-attomolar-level sensitivity.

Indexed as

Mass SpectrometryMetabolomicsPlant CellsSingle-Cell Analysis

Identifiers

PMID26313480

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.