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TMT Sample Preparation for Proteomics Facility Submission and Subsequent Data Analysis
Published on: June 8, 2020
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Serum proteome profiling in canine chronic valve disease using a TMT-based quantitative proteomics approach
Josipa Kuleš1, Petra Bilić1, Anita Horvatić1
1Clinic for Internal Diseases, Faculty of Veterinary Medicine, University of Zagreb, Croatia.
Journal of Proteomics
|May 19, 2020
Summary
This study identified 15 key serum proteins differing between healthy dogs and those with chronic valve disease (CVD). These findings offer insights into canine CVD biomarkers and comparative disease models.
Area of Science:
- Veterinary Medicine
- Proteomics
- Biomarker Discovery
Background:
- Chronic valve disease (CVD) is a prevalent heart condition in dogs, impacting 20-40% of the canine population.
- Understanding the molecular underpinnings of canine CVD is crucial for developing effective diagnostic and therapeutic strategies.
- Few studies have investigated the canine serum proteome for insights into cardiovascular disease.
Purpose of the Study:
- To evaluate the serum protein profile in healthy dogs versus dogs with CVD using a quantitative proteomic approach.
- To identify potential serum biomarkers associated with canine CVD.
- To explore the molecular mechanisms and pathways involved in canine CVD and compare them to human disease.
Main Methods:
- Employed isobaric tandem mass tag (TMT) label-based high-resolution quantitative proteomics.
- Measured conventional cardiac biomarkers in serum.
- Utilized functional bioinformatics for pathway analysis and validated proteomic findings via immunoassays and Western blotting.
Main Results:
- Identified and quantified 290 proteins, with 15 showing significantly different abundances (p < .05) between healthy and CVD dogs.
- Differentially abundant proteins include antithrombin-III, alpha-2-antiplasmin, tetranectin, apolipoprotein M, adiponectin, inter-alpha-trypsin inhibitor heavy chain H1, gelsolin, and apolipoprotein B-100.
- Identified proteins are involved in complement and coagulation cascades, hemostasis, actin cytoskeleton regulation, and lipid metabolism, showing similarities and differences with human CVD pathways.
Conclusions:
- Established serum proteomic signatures for healthy dogs and dogs with CVD.
- The findings contribute to understanding canine CVD etiology and provide potential novel biomarkers.
- The study highlights the value of canine CVD as a comparative model for human cardiovascular disease research.
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