Evidence map›Paper›PMID 27670688›Full record

ArticleMolecular & cellular proteomics : MCP2016

Simultaneous Proteomic Discovery and Targeted Monitoring using Liquid Chromatography, Ion Mobility Spectrometry, and Mass Spectrometry.

Kristin E Burnum-Johnson, Song Nie, Cameron P Casey, Matthew E Monroe, Daniel J Orton, Yehia M Ibrahim, Marina A Gritsenko, Therese R W Clauss, Anil K Shukla, Ronald J Moore and 6 more

Abstract readComparative Study
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
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  9. Review
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  13. Review
  14. Article
  15. Determination of Gas-Phase Ion Mobility Coefficients Using Voltage Sweep Multiplexing.Journal of the American Society for Mass Spectrometry · 2019
    Article
  16. Article
  17. Article
  18. Towards Discovery and Targeted Peptide Biomarker Detection Using nanoESI-TIMS-TOF MS.Journal of the American Society for Mass Spectrometry · 2018
    Article
  19. Review
  20. 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

16 authors.

Kristin E Burnum-JohnsonFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Song NieFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Cameron P CaseyFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Matthew E MonroeFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Daniel J OrtonFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Yehia M IbrahimFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Marina A GritsenkoFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Therese R W ClaussFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Anil K ShuklaFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Ronald J MooreFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Samuel O PurvineFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Tujin ShiFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Weijun QianFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Tao LiuFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington.
Erin S BakerFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington rds@pnnl.gov erin.baker@pnnl.gov.
Richard D SmithFrom the ‡Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington rds@pnnl.gov erin.baker@pnnl.gov.

Funding

Systems Biology Identifies Restriction Factors for West Nile VirusU19AI106772 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI SMITH, RICHARD D · 2013 to 2017
$26.1M
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
Platform Providing Increased Throughput, Sensitivity and Specificity for MetaboloR01ES022190 · NIEHS · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI BAKER, ERIN S · 2012 to 2016
$2.2M
NCI NIH HHS U24 CA160019NIAID NIH HHS U19 AI106772NIEHS NIH HHS R01 ES022190NIGMS NIH HHS P41 GM103493
6 · The paper itself

Abstract

Current proteomic approaches include both broad discovery measurements and quantitative targeted analyses. In many cases, discovery measurements are initially used to identify potentially important proteins (e.g. candidate biomarkers) and then targeted studies are employed to quantify a limited number of selected proteins. Both approaches, however, suffer from limitations. Discovery measurements aim to sample the whole proteome but have lower sensitivity, accuracy, and quantitation precision than targeted approaches, whereas targeted measurements are significantly more sensitive but only sample a limited portion of the proteome. Herein, we describe a new approach that performs both discovery and targeted monitoring (DTM) in a single analysis by combining liquid chromatography, ion mobility spectrometry and mass spectrometry (LC-IMS-MS). In DTM, heavy labeled target peptides are spiked into tryptic digests and both the labeled and unlabeled peptides are detected using LC-IMS-MS instrumentation. Compared with the broad LC-MS discovery measurements, DTM yields greater peptide/protein coverage and detects lower abundance species. DTM also achieved detection limits similar to selected reaction monitoring (SRM) indicating its potential for combined high quality discovery and targeted analyses, which is a significant step toward the convergence of discovery and targeted approaches.

Indexed as

AnimalsBreast NeoplasmsChromatography, LiquidFemaleHumansMass SpectrometryMiceNeoplasm TransplantationPeptidesProteomeProteomicsPeptidesProteome

Identifiers

PMID27670688
PMCPMC5141281

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.