Validation of hepcidin quantification in plasma using LC–HRMS and discovery of a new hepcidin isoform

Author:

Rochat Bertrand1,Peduzzi Davide2,McMullen Justin2,Favre Amélie2,Kottelat Emmanuel2,Favrat Bernard3,Tissot Jean-Daniel4,Angelillo-Scherrer Anne5,Bromirski Maciej6,Waldvogel Sophie4

Affiliation:

1. Quantitative Mass Spectrometry Facility University of Lausanne –CHUV, Route du Bugnon, BH18-218, 1011 Lausanne, Switzerland.

2. Quantitative Mass Spectrometry Facility University of Lausanne –CHUV, Route du Bugnon, BH18-218, 1011 Lausanne, Switzerland

3. Department of Ambulatory Care & Community Medicine, University of Lausanne –CHUV, Route du Bugnon, BH18-218, 1011 Lausanne, Switzerland

4. Service regional vaudois de transfusion sanguine, Epalinges, Switzerland

5. Service & Central Laboratory of Hematology, CHUV, Route de la Corniche, 1066 Epalinges, Switzerland

6. Thermo Scientific, Hanna-Kunath-Str. 11, 28199 Bremen, Germany

Abstract

Background: Hepcidin, a 25 amino acid peptide, plays an important role in iron homeostasis. Some hepcidin truncated peptides have antibiotic effects. Results: A new analytical method for hepcidin determination in human plasma using LC–HRMS operating in full-scan acquisition mode has been validated. The extraction consists of protein precipitation and a drying reconstitution step; a 2.1 x 50 mm (idxL) C18 analytical column was used. Detection specificity, stability, accuracy, precision and recoveries were determined. The LOQ/LOD were 0.25/0.1 nM, respectively. More than 600 injections of plasma extracts were performed, allowing evaluation of the assay robustness. Hepcidin-20, hepcidin-22 and a new isoform, hepcidin-24, were detected in patients. Conclusion: The data underscore the usefulness of LC–HRMS for in-depth investigations related to hepcidin levels and pathways.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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