Evidence map›Paper›PMID 24549895›Full record

ArticleJournal of the American Society for Mass Spectrometry2014

Mass spectral enhanced detection of Ubls using SWATH acquisition: MEDUSA--simultaneous quantification of SUMO and ubiquitin-derived isopeptides.

John R Griffiths, Navin Chicooree, Yvonne Connolly, Milla Neffling, Catherine S Lane, Thomas Knapman, Duncan L Smith

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of the American Society for Mass Spectrometry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

  1. Plasma-Derived Extracellular Vesicle Proteomics.Journal of proteome research · 2025
    Review
  2. Mass Spectrometry-based Solutions for Single-cell Proteomics.Genomics, proteomics & bioinformatics · 2025
    Review
  3. Review
  4. Article
  5. MS-Based Proteomics of Body Fluids: The End of the Beginning.Molecular & cellular proteomics : MCP · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Quantifying ubiquitin signaling.Molecular cell · 2015
    Review
  12. Article
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

7 authors at 1 institution in 1 country.

John R GriffithsCRUK Manchester Institute, University of Manchester, Manchester, M20 4BX, UK, john.griffiths@cruk.manchester.ac.uk.
Navin Chicooree
Yvonne Connolly
Milla Neffling
Catherine S Lane
Thomas Knapman
Duncan L Smith
University of Manchester · GB

Funding

Cancer Research UK
6 · The paper itself

Abstract

Protein modification by ubiquitination and SUMOylation occur throughout the cell and are responsible for numerous cellular functions such as apoptosis, DNA replication and repair, and gene transcription. Current methods for the identification of such modifications using mass spectrometry predominantly rely upon tryptic isopeptide tag generation followed by database searching with in vitro genetic mutation of SUMO routinely required. We have recently described a novel approach to ubiquitin and SUMO modification detection based upon the diagnostic a' and b' ions released from the isopeptide tags upon collision-induced dissociation of reductively methylated Ubl isopeptides (RUbI) using formaldehyde. Here, we significantly extend those studies by combining data-independent acquisition (DIA) with alternative labeling reagents to improve diagnostic ion coverage and enable relative quantification of modified peptides from both MS and MS/MS signals. Model synthetic ubiquitin and SUMO-derived isopeptides were labeled with mTRAQ reagents (Δ0, Δ4, and Δ8) and subjected to LC-MS/MS with SWATH acquisition. Novel diagnostic ions were generated upon CID, which facilitated the selective detection of these modified peptides. Simultaneous MS-based and MS/MS-based relative quantification was demonstrated for both Ub and SUMO-derived isopeptides across three channels in a background of mTRAQ-labeled Escherichia coli digest.

Indexed as

Models, MolecularAnalytic Sample Preparation MethodsChromatography, High Pressure LiquidElectrochemical TechniquesEscherichia coliEscherichia coli ProteinsIsotope LabelingMass SpectrometryOligopeptidesPeptidesProtein HydrolysatesSignal Processing, Computer-AssistedSumoylationTandem Mass SpectrometryUbiquitinated ProteinsEscherichia coli ProteinsOligopeptidesPeptidesProtein HydrolysatesUbiquitinated Proteins

Identifiers

PMID24549895
OpenAlexW1965532542

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.