Trypsin-like proteolytic contamination of commercially available psa purified from human seminal fluid

• Published in: The Prostate Vol. 72; no. 11; pp. 1233 - 1238
• Main Authors: Manning, Michael L., Kostova, Maya, Williams, Simon A., Denmeade, Samuel R.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-08-2012; Wiley-Liss
• Subjects: Biological and medical sciences; commercially; contamination; Drug Contamination; Gynecology. Andrology. Obstetrics; Humans; Mass Spectrometry; Medical sciences; Nephrology. Urinary tract diseases; Peptide Hydrolases - analysis; Prostate-Specific Antigen - analysis; PSA; Semen - chemistry; trypsin; Trypsin - analysis; Human; Andrology; Nephrology; Serine endopeptidases; Enzyme; Semen; Gynecology; Fluid; Tumoral marker; Contamination; Prostate specific antigen; commercially; Peptidases; Trypsin; Proteolysis; Hydrolases; PSA
• ISSN: 0270-4137; 1097-0045
• DOI: 10.1002/pros.22474

BACKGROUND
Prostate‐Specific Antigen (PSA) is a serine protease whose expression is maintained in all stages of prostate cancer. A role for PSA in the pathobiology for prostate cancer has not been firmly established. Experimental studies to date support a role for PSA through mechanisms such as release or processing of growth factors and degradation of the extracellular matrix. Exposure of prostate cancer cells to exogenous PSA also results in gene expression changes. These in vitro and biochemical assays rely on the use of commercially available PSA. Contamination of these commercial preparations can significantly impact the results of these in vitro studies.
METHODS
We characterized PSA and trypsin‐like activity of PSA preparations obtained from three commercial sources: Calbiochem, Fitzgerald, and AbD Serotec. Silver stained gels were used to compare the purity of each preparation and mass spectrometry was performed to characterize contaminating proteases.
RESULTS
PSA activity varied between PSA preparations with AbD Serotec PSA having highest degree of activity. Significant trypsin‐like activity, which was inhibited by aprotinin, was observed in PSA preparations from Calbiochem and Fitzgerald, but not AbD Serotec. These former two PSA preparations also contained the greatest degree of non‐PSA contaminants by silver stain and mass spectrometry.
CONCLUSIONS
Commercially available preparations of PSA contain contaminating proteins, including trypsin‐like protease activity, that could potentially complicate the interpretation of results obtained from in vitro studies assessing PSA proteolysis of potential protein substrates and effects of PSA on gene expression. Prostate 72:1233–1238, 2012. © 2011 Wiley Periodicals, Inc.