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Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Immunoluminometric assay for quantification of peroxiredoxin 4 in human serum
Janin Schulte1, Joachim Struck, Andreas Bergmann
1Research Department, BRAHMS AG (Part of ThermoFisher Scientific), Biotechnology Centre Hennigsdorf/Berlin, 16761 Hennigsdorf, Germany. j.schulte@brahms.de
Background:
We describe the validation of a novel assay for the measurement of peroxiredoxin 4 (Prx4), a potentially secreted antioxidant peroxidase, in human serum.
Methods:
A sandwich immunoluminometric assay (ILMA) was set up applying monoclonal antibodies against the amino-terminus of human Prx4. Prx4 levels have been determined in serum of healthy individuals and patients with sepsis and have been correlated to the clinically established sepsis marker procalcitonin (PCT).
Results:
The sandwich ILMA detected Prx4 in a range between 0.5 and 128 arbitrary (arb.) U/L and had a functional assay sensitivity of 0.51 arb.U/L. Serum Prx4 was stable for at least 72 h at 4 degrees C and 21 degrees C and circulated in a complex of about 330 kDa as characterized by size-exclusion chromatography. Patients with sepsis (n=45; median, 7.7 arb.U/L) showed significantly higher Prx4 serum levels (P<0.0001) than healthy controls (n=274; median, 0.71 arb.U/L). Serum Prx4 was positively correlated to PCT (r=0.63, P<0.0001).
Conclusion:
The newly developed assay reliably detected Prx4 in human serum of healthy and critically ill subjects. Elevated Prx4 in serum of patients with various diseases might serve as a biomarker reflecting increased oxidative stress.
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