Evidence map›Paper›PMID 19003867›Full record

ArticleProteomics2008

Two-dimensional electrophoresis-based characterization of post-translational modifications of mammalian 20S proteasome complexes.

Chenggong Zong, Glen W Young, Yueju Wang, Haojie Lu, Ning Deng, Oliver Drews, Peipei Ping

Open access · greenAbstract read
In one paragraph

Article in Proteomics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Review
  3. Known and Unexplored Post-Translational Modification Pathways in Schizophrenia.Advances in experimental medicine and biology · 2022
    Article
  4. Review
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  6. Review
  7. Review
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  9. Review
  10. Article
  11. Article
  12. Review
  13. Gel-based chemical cross-linking analysis of 20S proteasome subunit-subunit interactions in breast cancer.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2016
    Article
  14. Review
  15. Article
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  18. Article
  19. The ubiquitin proteasome system and myocardial ischemia.American journal of physiology. Heart and circulatory physiology · 2013
    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

7 authors at 2 institutions in 1 country.

Chenggong ZongDepartment of Physiology, University of California at Los Angeles, UCLA School of Medicine, Los Angeles, CA 90095, USA.
Glen W Young
Yueju Wang
Haojie Lu
Ning Deng
Oliver Drews
Peipei Ping
University of California, Los Angeles · USZero to Three · US

Funding

ROLE OF P38 MAPK AND PP2C IN ISCHEMIC INJURY AND PROTECTIONP01HL080111 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WEISS, JAMES N · 2005 to 2009
$11.6M
PKC EPSILON AND SRC PTK SIGNALING IN PRECONDITIONINGR01HL063901 · NHLBI · UNIVERSITY OF LOUISVILLE · PI PING, PEIPEI · 2000 to 2009
$3.3M
PKC epsilon and Src PTK Signaling in PreconditioningR37HL063901 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PING, PEIPEI · 2010 to 2016
$2.7M
SIGNALING MECHANISMS IN PHARMACOLOGIC PRECONDITIONINGR01HL065431 · NHLBI · UNIVERSITY OF LOUISVILLE · PI PING, PEIPEI · 2000 to 2008
$2.1M
NHLBI NIH HHS HL P01-80111NHLBI NIH HHS HL R01-63901NHLBI NIH HHS HL R01-65431NHLBI NIH HHS P01 HL080111NHLBI NIH HHS R01 HL063901NHLBI NIH HHS R01 HL065431NHLBI NIH HHS R37 HL063901
6 · The paper itself

Abstract

PTMs serve as key regulatory mechanisms for 20S proteasome functions. Alterations in 20S PTMs have been previously observed with changes in modified protein degradation patterns and altered cellular phenotypes. Despite decades of investigation, our knowledge pertaining to the various PTMs of 20S complexes and their biological significance remain limited. In this investigation, we show that 2-DE offers an analytical tool with high resolution and reproducibility. Accordingly, it has been applied for the characterization of PTMs including glycosylation, phosphorylation, oxidation, and nitrosylation. The PTMs of murine cardiac 20S proteasomes and their associating proteins were examined. Our 2-DE analyses displayed over 25 spots for the 20S complexes (17 subunits), indicating multiply modified subunits of cardiac proteasomes. The identification of specific PTM sites subsequent to 2-DE was supported by MS. These PTMs included phosphorylation and oxidation. Most of the PTMs occurred in low stoichiometry and required enrichment to enhance the detection sensitivity. In conclusion, our studies support 2-DE as a central tool in the analyses of 20S proteasome PTMs. The approaches utilized in this investigation demonstrate their application in mapping the PTMs of the 20S proteasomes in cardiac tissue, which are applicable to other samples and biological conditions.

Indexed as

Protein Processing, Post-TranslationalAmino Acid SequenceAnimalsElectrophoresis, Gel, Two-DimensionalGlycosylationImmunoblottingMammalsMass SpectrometryMiceMice, Inbred ICRMolecular Sequence DataMultiprotein ComplexesMyocardiumOxidation-ReductionPhosphoproteinsPhosphorylationMultiprotein ComplexesPhosphoproteinsProteasome Endopeptidase ComplexProtein SubunitsReactive Oxygen SpeciesSulfhydryl Compounds

Identifiers

PMID19003867
PMCPMC2674022
OpenAlexW2142064271

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.