Development of a sandwich ELISA for the 5.9-kDa fibrinogen alpha C chain fragment detected by serum proteome analysis

Purpose: We previously identified novel biomarker candidates in heavy consumers of alcohol using serum proteome analysis. Among several candidates, a 5.9 kDa peptide identified as a fragment of the fibrinogen alpha C chain (FIC5.9) was the most promising. To move FIC5.9 toward potential diagnostic u...

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Veröffentlicht in:Proteomics. Clinical applications 2011-04, Vol.5 (3-4), p.141-146
Hauptverfasser: Noda, Kenta, Sogawa, Kazuyuki, Kikuchi, Wataru, Kiyokawa, Iwao, Miura, Toshihide, Kojima, Ryo, Katayama, Katsuhiro, Kodera, Yoshio, Nomura, Fumio
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Sprache:eng
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Zusammenfassung:Purpose: We previously identified novel biomarker candidates in heavy consumers of alcohol using serum proteome analysis. Among several candidates, a 5.9 kDa peptide identified as a fragment of the fibrinogen alpha C chain (FIC5.9) was the most promising. To move FIC5.9 toward potential diagnostic use, we developed an enzyme immunoassay that enables measurement of serum FIC5.9 levels. Experimental design: Two monoclonal antibodies specific to the N and C‐termini of the 5.9‐kDa peptide were used to develop a FIC5.9 sandwich ELISA. The assay was evaluated by comparing the results with those obtained by the stable isotope‐labeled dilution mass spectrometry (SID‐MS) using the ClinProt™ system. Results: The ELISA results correlated with the SID‐MS findings (slope=0.795, intercept=−0.011, r2=0.908) and the performance of the ELISA was satisfactory in terms of recovery (98.5–103.0%) and within‐run (1.4–4.7%) and between‐day (2.8–8.4%) reproducibility. The assay was capable of detecting changes in FIC5.9 during abstinence from drinking in patients with alcohol dependency (p
ISSN:1862-8346
1862-8354
DOI:10.1002/prca.201000127