An Equine Protein Atlas Highlights Synovial Fluid Proteome Dynamics during Experimentally LPS-Induced Arthritis.
Abstract: In human proteomics, substantial efforts are ongoing to leverage large collections of mass spectrometry (MS) fragment ion spectra into extensive spectral libraries (SL) as a resource for data independent acquisition (DIA) analysis. Currently, such initiatives in equine research are still missing. Here we present a large-scale equine SL, comprising 6394 canonical proteins and 89,329 unique peptides, based on data dependent acquisition analysis of 75 tissue and body fluid samples from horses. The SL enabled large-scale DIA-MS based quantification of the same samples to generate a quantitative equine protein distribution atlas to infer dominant proteins in different organs and body fluids. Data mining revealed 163 proteins uniquely identified in a specific type of tissue or body fluid, serving as a starting point to determine tissue-specific or tissue-type-specific proteins. We showcase the SL by highlighting proteome dynamics in equine synovial fluid samples during experimental lipopolysaccharide-induced arthritis. A fuzzy c-means cluster analysis pinpointed SERPINB1, ATRN, NGAL, LTF, MMP1, and LBP as putative biomarkers for joint inflammation. This SL provides an extendable resource for future equine studies employing DIA-MS.
Publication Date: 2024-10-12 PubMed ID: 39395021DOI: 10.1021/acs.jproteome.4c00125Google Scholar: Lookup
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- Journal Article
Summary
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This study presents a large-scale library of proteins found in horses, allowing for deeper analysis of specific proteins in different organs and body fluids. The data assembled in the study has also been used to identify potential biomarkers for joint inflammation in horses.
Objective and Methods
- The study’s main aim was to compile a comprehensive catalog of proteins specific to horses, as similar resources are currently lacking in equine research.
- The researchers used data dependent acquisition (DDA) analysis on 75 horse tissue and body fluid samples to create a spectral library (SL) listing 6394 canonical proteins and 89,329 unique peptides.
- They then used data independent acquisition mass spectrometry (DIA-MS) to quantify these proteins, building a quantitative equine protein distribution atlas. This allows scientists to infer the most dominant proteins in different horse organs and body fluids.
Key Findings
- Data mining of the protein distribution atlas identified 163 proteins that were uniquely found in a specific type of tissue or body fluid. This information could help researchers discover tissue-specific or tissue-type-specific proteins in horses.
- The researchers used their spectral library to study changes in the protein make-up of horse synovial fluid (a type of joint fluid) during lipopolysaccharide-induced arthritis. This experiment mimics a type of joint inflammation common in horses.
- A fuzzy c-means cluster analysis was used to identify proteins that might indicate the presence of joint inflammation. Six proteins—SERPINB1, ATRN, NGAL, LTF, MMP1, and LBP—were flagged as potential biomarkers for this condition.
Implications and Future Research
- This study’s creation of a large-scale spectral library for equine proteins can serve as a powerful resource for future research on horses. Its data can be used to study various aspects of equine biology at a molecular level, potentially leading to more effective treatment strategies for different diseases.
- The identified potential biomarkers for joint inflammation are particularly relevant due to arthritis being a common ailment in horses. Watching for changes in the levels of these proteins could aid in early detection and management of the disease.
Cite This Article
APA
Bundgaard L, Årman F, Åhrman E, Walters M, Auf dem Keller U, Malmström J, Jacobsen S.
(2024).
An Equine Protein Atlas Highlights Synovial Fluid Proteome Dynamics during Experimentally LPS-Induced Arthritis.
J Proteome Res.
https://doi.org/10.1021/acs.jproteome.4c00125 Publication
Researcher Affiliations
- Section of Medicine and Surgery, Department of Veterinary Clinical Sciences, University of Copenhagen, 2630 Taastrup, Denmark.
- Department of Biotechnology and Biomedicine, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.
- Division of Infection Medicine Proteomics, Department of Clinical Sciences, Lund University, 221 84 Lund, Sweden.
- Division of Infection Medicine Proteomics, Department of Clinical Sciences, Lund University, 221 84 Lund, Sweden.
- Section of Medicine and Surgery, Department of Veterinary Clinical Sciences, University of Copenhagen, 2630 Taastrup, Denmark.
- Department of Biotechnology and Biomedicine, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.
- Division of Infection Medicine Proteomics, Department of Clinical Sciences, Lund University, 221 84 Lund, Sweden.
- Section of Medicine and Surgery, Department of Veterinary Clinical Sciences, University of Copenhagen, 2630 Taastrup, Denmark.
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