Evidence map›Paper›PMID 22038862›Full record

ArticleProteomics2011

Proteomic analysis of Col11a1-associated protein complexes.

Raquel J Brown, Christopher Mallory, Owen M McDougal, Julia Thom Oxford

Open access · bronzeAbstract read
In one paragraph

Article in Proteomics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Proteomics analysis of the matrisome from MC38 experimental mouse liver metastases.American journal of physiology. Gastrointestinal and liver physiology · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Proteomic Analysis of Engineered Cartilage.Methods in molecular biology (Clifton, N.J.) · 2015
    Article
  13. Article
  14. Defining the extracellular matrix using proteomics.International journal of experimental pathology · 2013
    Review
  15. 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

4 authors at 1 institution in 1 country.

Raquel J BrownDepartment of Biological Sciences, Biomolecular Research Center and Musculoskeletal Research Institute, Boise State University, Boise, ID 83725-1515, USA.
Christopher Mallory
Owen M McDougal
Julia Thom Oxford
Boise State University · US

Funding

UNDERGRADUATE COLLEGE OUTREACH PROGRAMP20RR016454 · NCRR · UNIVERSITY OF IDAHO · PI CHASE, JENNIFER R · 2001 to 2011
$35.3M
VPS35 D620N inhibits autophagy through disrupted hyaluronic acid-CD44 signalingP20GM109095 · NIGMS · BOISE STATE UNIVERSITY · PI THEODOSSIOU, SOPHIA KATERINA · 2014 to 2023
$22.7M
Type XI collagen isoforms in skeletal biologyR01AR047985 · NIAMS · BOISE STATE UNIVERSITY · PI OXFORD, JULIA T · 2001 to 2005
$1.3M
Type XI collagen isoforms in skeletal biologyK02AR048672 · NIAMS · BOISE STATE UNIVERSITY · PI OXFORD, JULIA T · 2002 to 2006
$376k
Regulation of cell signaling by Col11a1 during craniofacial development in the zeR15HD059949 · NICHD · BOISE STATE UNIVERSITY · PI OXFORD, JULIA THOM · 2009 to 2009
$212k
NCRR NIH HHS P20 RR016454NCRR NIH HHS P20RR16454NIAMS NIH HHS K02 AR048672NIAMS NIH HHS K02AR48672NIAMS NIH HHS R01 AR047985NIAMS NIH HHS R01AR47985NICHD NIH HHS R15 HD059949NIGMS NIH HHS P20 GM109095
6 · The paper itself

Abstract

Cartilage plays an essential role during skeletal development within the growth plate and in articular joint function. Interactions between the collagen fibrils and other extracellular matrix molecules maintain structural integrity of cartilage, orchestrate complex dynamic events during embryonic development, and help to regulate fibrillogenesis. To increase our understanding of these events, affinity chromatography and liquid chromatography/tandem mass spectrometry were used to identify proteins that interact with the collagen fibril surface via the amino terminal domain of collagen α1(XI) a protein domain that is displayed at the surface of heterotypic collagen fibrils of cartilage. Proteins extracted from fetal bovine cartilage using homogenization in high ionic strength buffer were selected based on affinity for the amino terminal noncollagenous domain of collagen α1(XI). MS was used to determine the amino acid sequence of tryptic fragments for protein identification. Extracellular matrix molecules and cellular proteins that were identified as interacting with the amino terminal domain of collagen α1(XI) directly or indirectly, included proteoglycans, collagens, and matricellular molecules, some of which also play a role in fibrillogenesis, while others are known to function in the maintenance of tissue integrity. Characterization of these molecular interactions will provide a more thorough understanding of how the extracellular matrix molecules of cartilage interact and what role collagen XI plays in the process of fibrillogenesis and maintenance of tissue integrity. Such information will aid tissue engineering and cartilage regeneration efforts to treat cartilage tissue damage and degeneration.

Indexed as

Amino Acid SequenceAnimalsCartilageCattleCollagen Type XIExtracellular MatrixModels, MolecularMolecular Sequence DataProtein Structure, TertiaryProteomicsSequence AlignmentSequence Analysis, ProteinCollagen Type XI

Identifiers

PMID22038862
PMCPMC3463621
OpenAlexW2055558880

What OpenQuestion holds

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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.