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Recently scientists reported that the same proteins, regardless of tissue or species, are often found expressed differentially in disease states, bringing into question the significance of these proteins as potential biomarkers.1, 2
Scientists at Denator have drawn on data from studies investigating post-mortem changes in proteomic profiles to reveal a remarkable overlap between the proteins commonly identified as changing in these studies and those proteins found to change post-mortem.3
1.Deja vu in proteomics. A hit parade of repeatedly identified differentially expressed proteins. Petrak et al., Proteomics. 2008;8:1744-9
2. Generally detected proteins in comparative proteomics--a matter of cellular stress response?. Wang P. et al., Proteomics. 2009;9:2955-66
3. Biomarkers of disease and post-mortem changes — Heat stabilization, a necessary tool for measurement of protein regulation. Kultima K. et al., J Proteomics. 2011
What do these proteins have in common?When compared with typical levels reported in the literature4 they show a clear over-representation of phosphorylation sites, indicating that the detected regulation of these proteins is due to changes in post-translational modifications after tissue sampling. Full details of this investigation were presented in a scientific poster presented at HUPO 2011 (download) 4. The protein kinase complement of the human genome. Manning G, et al.,Science. 2002 Dec 6;298 (5600):1912-34. Review.
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POSTER Changes in phosphorylation states post-mortem may distort our view of in vivo proteomic profiles Download
(PDF, 5.9 MB)
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Rapid heat stabilization instantly and permanently stops enzymatic activity, preventing post-mortem changes and thereby revealing results closer to the actual in vivo profile. This approach may help to differentiate true biomarkers from those proteins found in any situation where cells are under stress.
To view a comprehensive list of proteins that may indicate post-mortem changes, click here
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