Evidence map›Paper›PMID 26015166›Full record

ArticleJournal of the American Society for Mass Spectrometry2015

An Optimized Informatics Pipeline for Mass Spectrometry-Based Peptidomics.

Chaochao Wu, Matthew E Monroe, Zhe Xu, Gordon W Slysz, Samuel H Payne, Karin D Rodland, Tao Liu, Richard D Smith

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society for Mass Spectrometry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Origins, Technological Advancement, and Applications of Peptidomics.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  2. Article
  3. Review
  4. Review
  5. 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

8 authors at 1 institution in 1 country.

Chaochao WuBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Matthew E MonroeBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Zhe XuBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Gordon W SlyszBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Samuel H PayneBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Karin D RodlandBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Tao LiuBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99352, USA. tao.liu@pnnl.gov.
Richard D SmithBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99352, USA. dick.smith@pnnl.gov.
Pacific Northwest National Laboratory · US

Funding

Equipment Supplement Request for a Research Resource for Ultra-sensitive High Throughput ProteomicsP41GM103493 · NIGMS · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI SMITH, RICHARD D · 2012 to 2022
$22.6M
PNNL Clinical Proteome Characterization CenterU24CA160019 · NCI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI RODLAND, KARIN D, SMITH, RICHARD D · 2011 to 2016
$15.7M
NCI NIH HHS U24 CA160019NCI NIH HHS U24CA160019NIGMS NIH HHS P41 GM103493NIGMS NIH HHS P41GM103493
6 · The paper itself

Abstract

The comprehensive MS analysis of the peptidome, the intracellular and intercellular products of protein degradation, has the potential to provide novel insights on endogenous proteolytic processing and its utility in disease diagnosis and prognosis. Along with the advances in MS instrumentation and related platforms, a plethora of proteomics data analysis tools have been applied for direct use in peptidomics; however, an evaluation of the currently available informatics pipelines for peptidomics data analysis has yet to be reported. In this study, we began by evaluating the results of several popular MS/MS database search engines, including MS-GF+, SEQUEST, and MS-Align+, for peptidomics data analysis, followed by identification and label-free quantification using the well-established accurate mass and time (AMT) tag and newly developed informed quantification (IQ) approaches, both based on direct LC-MS analysis. Our results demonstrated that MS-GF+ outperformed both SEQUEST and MS-Align+ in identifying peptidome peptides. Using a database established from MS-GF+ peptide identifications, both the AMT tag and IQ approaches provided significantly deeper peptidome coverage and less missing data for each individual data set than the MS/MS methods, while achieving robust label-free quantification. Besides having an excellent correlation with the AMT tag quantification results, IQ also provided slightly higher peptidome coverage. Taken together, we propose an optimized informatics pipeline combining MS-GF+ for initial database searching with IQ (or AMT tag) approaches for identification and label-free quantification for high-throughput, comprehensive, and quantitative peptidomics analysis. Graphical Abstract ᅟ.

Indexed as

Chromatography, LiquidDatabases, ProteinHumansNeoplasmsPeptide MappingPeptidesProteomicsSearch EngineSoftwareTandem Mass SpectrometryWorkflowPeptidesAccurate mass and time tagIdentificationInformed quantitationMS-GF+PeptidomicsQuantification

Identifiers

PMID26015166
PMCPMC4655184
OpenAlexW366671363

What OpenQuestion holds

Textmetadata
LicenceTDM
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.