Proteomics analysis of human coronary atherosclerotic plaque: a feasibility study of direct tissue proteomics by liquid chromatography and tandem mass spectrometry

• Published in: Molecular & cellular proteomics 2007-06, Vol.6 (6), p.1088-1102
• Main Authors: Bagnato, Carolina, Thumar, Jaykumar, Mayya, Viveka, Hwang, Sun-Il, Zebroski, Henry, Claffey, Kevin P, Haudenschild, Christian, Eng, Jimmy K, Lundgren, Deborah H, Han, David K
• Format: Article
• Language: English
• Subjects: Annexin A1 - metabolism; Antigens, Surface - metabolism; Atherosclerosis - metabolism; Atherosclerosis - pathology; Cell Adhesion Molecules - metabolism; Chromatography, Liquid; Coronary Vessels - chemistry; Cytokines - analysis; Extracellular Matrix Proteins - metabolism; Eye Proteins - chemistry; Eye Proteins - metabolism; Feasibility Studies; Humans; Inflammation Mediators - metabolism; Intercellular Signaling Peptides and Proteins - analysis; Ligands; Microdissection; Milk Proteins - metabolism; Nerve Growth Factors - chemistry; Nerve Growth Factors - metabolism; Phagocytosis; Proteome - analysis; Proteomics; Reproducibility of Results; Serpins - chemistry; Serpins - metabolism; Tandem Mass Spectrometry
• ISSN: 1535-9476
• DOI: 10.1074/mcp.M600259-MCP200

Cardiovascular disease presents significant variations in human populations with respect to the atherosclerotic plaque progression, inflammation, thrombosis, and rupture. To gain a more comprehensive picture of the pathogenic mechanism of atherosclerosis and the variations seen in patients, efficient methods to identify proteins from the normal and diseased arteries need to be developed. To accomplish this goal, we tested the feasibility and efficiency of protein identification by a recently developed method, termed direct tissue proteomics (DTP). We analyzed frozen and paraformaldehyde-fixed archival coronary arteries with the DTP method. We also validated the distinct expression of four proteins by immunohistochemistry. In addition, we demonstrated the compatibility of the DTP method with laser capture microdissection and the possibility of monitoring specific cytokines and growth factors by the absolute quantification of abundance method. Major findings from this feasibility study are that 1) DTP can be used to efficiently identify proteins from paraformaldehyde-fixed, paraffin-embedded, and frozen coronary arteries; 2) approximately twice the number of proteins were identified from the frozen sections when compared with the paraformaldehyde-fixed sections; 3) laser capture microdissection is compatible with DTP; and 4) detection of low abundance cytokines and growth factors in the coronary arteries required selective reaction monitoring experiments coupled to absolute quantification of abundance. The analysis of 35 human coronary atherosclerotic samples allowed identification of a total of 806 proteins. The present study provides the first large scale proteomics map of human coronary atherosclerotic plaques.