Evidence map›Paper›PMID 25025725›Full record

ArticleJournal of proteome research2014

Identification and Quantitation of Coding Variants and Isoforms of Pulmonary Surfactant Protein A.

Matthew W Foster, J Will Thompson, Julie G Ledford, Laura G Dubois, John W Hollingsworth, Dave Francisco, Sasipa Tanyaratsrisakul, Dennis R Voelker, Monica Kraft, M Arthur Moseley and 1 more

Abstract read
In one paragraph

Article in Journal of proteome research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

11 authors at 2 institutions in 1 country.

Matthew W Foster
J Will Thompson
Julie G Ledford
Laura G Dubois
John W Hollingsworth
Dave Francisco
Sasipa Tanyaratsrisakul‡Department of Medicine, National Jewish Health, Denver, Colorado 80206, United States.
Dennis R Voelker‡Department of Medicine, National Jewish Health, Denver, Colorado 80206, United States.
Monica Kraft
M Arthur Moseley
W Michael Foster
National Jewish Health · USUniversity of Colorado Denver · US

Funding

Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI Trevor M Penning · 2006 to 2026
$35.3M
Surfactant Protein-A Regulation of Innate Immunityin AsthmaP01AI081672 · NIAID · DUKE UNIVERSITY · PI KRAFT, MONICA · 2009 to 2013
$7.4M
The role of SP-A in Mp-induced exacerbations during allergic airway disease.R00HL111151 · NHLBI · UNIVERSITY OF ARIZONA · PI LEDFORD, JULIE GUNNELLS · 2014 to 2016
$716k
The role of SP-A in Mp-induced exacerbations during allergic airway disease.K99HL111151 · NHLBI · DUKE UNIVERSITY · PI LEDFORD, JULIE GUNNELLS · 2012 to 2013
$201k
NHLBI NIH HHS HL111151NHLBI NIH HHS K99 HL111151NHLBI NIH HHS R00 HL111151NIAID NIH HHS AI081672NIAID NIH HHS P01 AI081672NIEHS NIH HHS P30 ES013508
6 · The paper itself

Abstract

Pulmonary surfactant protein A (SP-A), a heterooligomer of SP-A1 and SP-A2, is an important regulator of innate immunity of the lung. Nonsynonymous single nucleotide variants of SP-A have been linked to respiratory diseases, but the expressed repertoire of SP-A protein in human airway has not been investigated. Here, we used parallel trypsin and Glu-C digestion, followed by LC-MS/MS, to obtain sequence coverage of common SP-A variants and isoform-determining peptides. We further developed a SDS-PAGE-based, multiple reaction monitoring (GeLC-MRM) assay for enrichment and targeted quantitation of total SP-A, the SP-A2 isoform, and the Gln223 and Lys223 variants of SP-A, from as little as one milliliter of bronchoalveolar lavage fluid. This assay identified individuals with the three genotypes at the 223 position of SP-A2: homozygous major (Gln223/Gln223), homozygous minor (Lys223/Lys223), or heterozygous (Gln223/Lys223). More generally, our studies demonstrate the challenges inherent in distinguishing highly homologous, copurifying protein isoforms by MS and show the applicability of MRM mass spectrometry for identification and quantitation of nonsynonymous single nucleotide variants and other proteoforms in airway lining fluid.

Indexed as

AdolescentAdultAmino Acid SequenceBronchoalveolar LavageBronchoalveolar Lavage FluidChromatography, LiquidGenetic VariationGenotypeHealthy VolunteersHeterozygoteHumansLungMass SpectrometryMolecular Sequence DataPeptidesPolymorphism, Single Nucleotideglutamyl endopeptidasePeptidesProtein IsoformsPulmonary Surfactant-Associated Protein ASerine EndopeptidasesSFTPA1 protein, humanSFTPA2 protein, humanTrypsinallelic variantionKeyrs1965708surfactant-associated proteintargeted proteomics

Identifiers

PMID25025725
PMCPMC4123939
OpenAlexW2319479397

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.