Cost-Effective Simultaneous Determination of τ- and π-Methylhistidine in Dairy Bovine Plasma from Large Cohort Studies Using Hydrophilic Interaction Ultra-High Performance Liquid Chromatography Coupled to Tandem Mass Spectrometry

Author:

Sampsonidis Ioannis12ORCID,Marinaki Maria234,Pesiridou Anastasia234,Gika Helen245ORCID,Theodoridis Georgios234ORCID,Siachos Nektarios6ORCID,Arsenos Georgios6ORCID,Kalogiannis Stavros12ORCID

Affiliation:

1. Department of Nutritional Sciences and Dietetics, International Hellenic University, Sindos Campus, GR57400 Thessaloniki, Greece

2. FoodOmicsGR Research Infrastructure, AUTh Node, Center for Interdisciplinary Research and Innovation (CIRI-AUTH), Balkan Center B1.4, 10th Km Thessaloniki-Thermi Rd., P.O. Box 8318, GR57001 Thessaloniki, Greece

3. Department of Chemistry, Faculty of Sciences, Aristotle University of Thessaloniki, GR54124 Thessaloniki, Greece

4. Biomic AUTh, Center for Interdisciplinary Research and Innovation (CIRI-AUTH), Balkan Center B1.4, 10th Km Thessaloniki-Thermi Rd., P.O. Box 8318, GR57001 Thessaloniki, Greece

5. School of Medicine, Aristotle University of Thessaloniki, GR54124 Thessaloniki, Greece

6. Laboratory of Animal Husbandry, Faculty of Veterinary Medicine, School of Health Sciences, Aristotle University of Thessaloniki, GR54124 Thessaloniki, Greece

Abstract

The isomeric metabolites τ- and π-methylhistidine (formerly referred to as 3- and 1-methylhistidine) are known biomarkers for muscle protein breakdown and meat protein intake, frequently used in studies involving humans and animals. In the present study, we report the development and validation of a simple HILIC-MS/MS method for individual determination of τ-MH and π-MH in a large cohort of blood plasma samples from dairy cows. Their separate determination was achieved mainly through a mass spectrometry fragment ion study, which revealed that the two isomers exhibited distinct mass spectrometric behaviors at different collision energies. Chromatographic conditions were optimised to achieve better separation, minimizing inter-channel interference to less than 1% in both directions. A simple and effective sample clean-up method facilitated low laboratory manual workload. The analytical method was validated for the determination of τ-MH and π-MH in bovine plasma within a concentration range of 80 to 1600 μg/L and provided good linearity (>0.99 for both curves) and precision (<10%). Overall, the developed method enabled the determination of the two isomers in an efficient and economic-friendly manner suitable for large cohort bovine studies (involving hundreds to thousands of samples) mainly to provide data for statistical use.

Funder

Operational Programme “Competitiveness, Entrepreneurship and Innovation”

Greece and the European Union

Publisher

MDPI AG

Subject

Filtration and Separation,Analytical Chemistry

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