Evidence map›Paper›PMID 31050378›Full record

ReviewProteomics2019

Identification and Quantification of Proteoforms by Mass Spectrometry.

Leah V Schaffer, Robert J Millikin, Rachel M Miller, Lissa C Anderson, Ryan T Fellers, Ying Ge, Neil L Kelleher, Richard D LeDuc, Xiaowen Liu, Samuel H Payne and 9 more

Abstract readReview
In one paragraph

Review in Proteomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing 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

117 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Capillary Electrophoresis-Mass Spectrometry for Top-Down Proteomics.Annual review of analytical chemistry (Palo Alto, Calif.) · 2025
    Review
  19. Review
  20. Article

57 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

19 authors.

Leah V SchafferDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Robert J MillikinDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Rachel M MillerDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Lissa C AndersonIon Cyclotron Resonance Program, National High Magnetic Field Laboratory, Tallahassee, FL, 32310, USA.
Ryan T FellersProteomics Center of Excellence, Northwestern University, Evanston, IL, 60208, USA.
Ying GeDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Neil L KelleherProteomics Center of Excellence, Northwestern University, Evanston, IL, 60208, USA.
Richard D LeDucProteomics Center of Excellence, Northwestern University, Evanston, IL, 60208, USA.
Xiaowen LiuDepartment of BioHealth Informatics, Indiana University-Purdue University, Indianapolis, IN, 46202, USA.
Samuel H PayneDepartment of Biology, Brigham Young University, Provo, UT, 84602.
Liangliang SunDepartment of Chemistry, Michigan State University, East Lansing, MI, 48824, USA.
Paul M ThomasProteomics Center of Excellence, Northwestern University, Evanston, IL, 60208, USA.
Trisha TucholskiDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Zhe WangDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, OK, 73019, USA.
Si WuDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, OK, 73019, USA.
Zhijie WuDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Dahang YuDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, OK, 73019, USA.
Michael R ShortreedDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Lloyd M SmithDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.

Funding

BIOTECHNOLOGY TRAINING PROGRAMT32GM008349 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI FOX, BRIAN G · 1989 to 2019
$22.5M
Institutional Training in the Genomic SciencesT32HG002760 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI Qiongshi Lu · 2003 to 2026
$17.7M
TR&D 7: Cell Specific ProteomicsP41GM108569 · NIGMS · NORTHWESTERN UNIVERSITY · PI KELLEHER, NEIL L · 2015 to 2024
$13.6M
Chemistry-Biology Interface Training ProgramT32GM008505 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI BLACKWELL, HELEN E. · 1993 to 2023
$9.8M
Revealing Proteoforms: The Primary Effectors of Biological FunctionR35GM126914 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Lloyd M Smith · 2018 to 2026
$6.2M
Deciphering Myofilament Modifications in Ischemic CardiomyopathyR01HL109810 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI GE, YING · 2013 to 2024
$3.5M
Top Down Proteomics Of Myofilaments In Heart FailureR01HL096971 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI GE, YING · 2011 to 2021
$3.3M
Computational tools for top down mass spectrometry based proteoform identification and proteogenomicsR01GM118470 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI Xiaowen Liu · 2016 to 2026
$2.7M
Enabling Top-Down Proteomics through Materials Chemistry and NanotechnologyR01GM117058 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI GE, YING, JIN, SONG · 2015 to 2023
$2.7M
Ultra High Resolution Mass Spectrometer for Biomedical ResearchS10OD018475 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI GE, YING · 2015 to 2015
$2.0M
Quantitative proteomics of Zebrafish embryos and blastomeresR01GM125991 · NIGMS · MICHIGAN STATE UNIVERSITY · PI SUN, LIANGLIANG · 2018 to 2022
$1.7M
Intact Proteoform Identification and QuantificationR01GM114292 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI GOULD, MICHAEL N, SMITH, LLOYD M · 2015 to 2018
$1.6M
NHGRI NIH HHS 5T32HG002760NHGRI NIH HHS T32 HG002760NHLBI NIH HHS R01 HL096971NHLBI NIH HHS R01 HL109810NIGMS NIH HHS P41 GM108569NIGMS NIH HHS P41GM108569NIGMS NIH HHS R01 GM114292NIGMS NIH HHS R01GM114292NIGMS NIH HHS R01 GM117058NIGMS NIH HHS R01 GM118470NIGMS NIH HHS R01 GM125085NIGMS NIH HHS R01 GM125991NIGMS NIH HHS R35 GM126914NIGMS NIH HHS R35GM126914NIGMS NIH HHS T32 GM008349NIGMS NIH HHS T32GM008349NIGMS NIH HHS T32 GM008505NIGMS NIH HHS T32GM008505NIH HHS R01GM117058NIH HHS R01GM118470NIH HHS R01GM125085NIH HHS R01GM125991NIH HHS R01HL096971NIH HHS R01HL109810NIH HHS S10 OD018475NIH HHS S10OD018475
6 · The paper itself

Abstract

A proteoform is a defined form of a protein derived from a given gene with a specific amino acid sequence and localized post-translational modifications. In top-down proteomic analyses, proteoforms are identified and quantified through mass spectrometric analysis of intact proteins. Recent technological developments have enabled comprehensive proteoform analyses in complex samples, and an increasing number of laboratories are adopting top-down proteomic workflows. In this review, some recent advances are outlined and current challenges and future directions for the field are discussed.

Indexed as

Mass SpectrometryProtein Processing, Post-TranslationalAmino AcidsAnimalsComputational BiologyElectrophoresis, CapillaryHumansProgramming LanguagesProteomeProteomicsReproducibility of ResultsSoftwareAmino AcidsProteomebioinformaticsmass spectrometryproteoformproteoform familytop-down proteomics

Identifiers

PMID31050378
PMCPMC6602557

What OpenQuestion holds

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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.