Evidence map›Paper›PMID 19833730›Full record

ArticleThe Journal of biological chemistry2009

Structural characterization of mouse neutrophil serine proteases and identification of their substrate specificities: relevance to mouse models of human inflammatory diseases.

Timofey Kalupov, Michèle Brillard-Bourdet, Sébastien Dadé, Hélène Serrano, Julien Wartelle, Nicolas Guyot, Luiz Juliano, Thierry Moreau, Azzaq Belaaouaj, Francis Gauthier

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. Establishment of a Risk Score Model for Early Prediction of Severe H1N1 Influenza.Frontiers in cellular and infection microbiology · 2021
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Mast cell proteases as pharmacological targets.European journal of pharmacology · 2016
    Review
  9. Article
  10. Staphylococcus aureus secretes a unique class of neutrophil serine protease inhibitors.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  11. The porcine innate immune system: an update.Developmental and comparative immunology · 2014
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
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

10 authors at 5 institutions in 2 countries.

Timofey KalupovINSERM U618, Protéases et Vectorisation Pulmonaires, IFR 135, Université François Rabelais de Tours, 37032 Tours, France.
Michèle Brillard-Bourdet
Sébastien Dadé
Hélène Serrano
Julien Wartelle
Nicolas Guyot
Luiz Juliano
Thierry Moreau
Azzaq Belaaouaj
Francis Gauthier
Hôpital Maison Blanche · FRUniversité de Tours · FRInserm · FRCentre Hospitalier Universitaire de Reims · FRUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is widely accepted that neutrophil serine proteases (NSPs) play a critical role in neutrophil-associated lung inflammatory and tissue-destructive diseases. To investigate NSP pathogenic role(s), various mouse experimental models have been developed that mimic acutely or chronically injured human lungs. We and others are using mouse exposure to cigarette smoke as a model for chronic obstructive pulmonary disease with or without exacerbation. However, the relative contribution of NSPs to lung disease processes as well as their underlying mechanisms remains still poorly understood. And the lack of purified mouse NSPs and their specific substrates have hampered advances in these studies. In this work, we compared mouse and human NSPs and generated three-dimensional models of murine NSPs based on three-dimensional structures of their human homologs. Analyses of these models provided compelling evidence that peptide substrate specificities of human and mouse NSPs are different despite their conserved cleft and close structural resemblance. These studies allowed us to synthesize for the first time novel sensitive fluorescence resonance energy transfer substrates for individual mouse NSPs. Our findings and the newly identified substrates should better our understanding about the role of NSPs in the pathogenesis of cigarette-associated chronic obstructive pulmonary disease as well as other neutrophils-associated inflammatory diseases.

Indexed as

AnimalsCathepsinsFluorescence Resonance Energy TransferHumansInflammationKineticsMiceMolecular ConformationNeutrophilsPeptidesProtein ConformationSerine ProteasesSmokingSpecies SpecificitySubstrate SpecificityCathepsinsPeptidesSerine Proteases

Identifiers

PMID19833730
PMCPMC2797179
OpenAlexW1980295808

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.