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Capillary Electrophoresis for Amino Acids Analysis: From Analytical Development to Biomedical Application

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Biophysics".

Deadline for manuscript submissions: closed (30 June 2021) | Viewed by 4756

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Guest Editor
Laboratoire des IMRCP, Université Paul Sabatier, Université de Toulouse, 31062 Toulouse, France
Interests: mass spectrometry of biological molecules; quantitative analytical biochemistry; trace analysis

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Guest Editor
Laboratoire des IMRCP, Université de Toulouse, CNRS UMR 5623, Université Toulouse III—Paul Sabatier, F-31062 Toulouse, France
Interests: oxidative stress; Alzheimer’s disease; mass spectrometry
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Guest Editor
Department of Hygiene, Third Faculty of Medicine, Charles University, Ruská 87, 100 00, Prague 10, Czech Republic

Special Issue Information

Dear Colleagues,

Amino acids (AAs) are essential building bricks of proteins and are encoded by RNAt. The 20 usual AAs are well known and differ from each other by the nature of the side chain. L-AAs are widely found in living organisms, but the interest in D-AAs has become more important for biologists in recent years. Modified AAs are also present in biological media, resulting from a post-transcriptional modification or a different metabolic pathway (methylation, hydroxylation, acetylation, etc.) or a metabolization (decarboxylation, demethylation, dehydration, etc.). The knowledge of their concentrations in vivo is important to understand their metabolism or catabolism in relation with a specific pathology, for their biological implications and for medical diagnosis.

Several analytical techniques allow the detection and quantification of AAs, but capillary electrophoresis (CE) presents the main advantages of being highly sensitive and not expensive, allowing enantiomeric separation with high resolution. Thus, CE is a technique of choice for AA’s analysis and is successfully applied in several application domains and contexts.

This Special Issue will cover the most important evolutions in CE analysis during the last few years. It will focus on the analysis of amino acids by CE coupled to conductivity, fluorescence or mass spectrometry, from analytical development to biomedical applications.

Subtopics include, but are not limited to:

  • CE development and coupling with MS for the analysis of amino acids;
  • Specific detection of D-amino acids by CE;
  • CE/conductimetry and CE/fluorescence for amino acids analysis;
  • CE for biomedical applications.

Prof. Dr. François Couderc
Prof. Dr. Fabrice Collin
Prof. Dr. Petr Tuma
Guest Editors

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Keywords

  • amino acids
  • capillary electrophoresis
  • enantiomeric separation
  • CE/MS

Published Papers (2 papers)

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20 pages, 2436 KiB  
Article
Determination of Branched-Chain Amino Acids in Food Supplements and Human Plasma by a CE-MS/MS Method with Enhanced Resolution
by Juraj Piestansky, Michaela Matuskova, Ivana Cizmarova, Dominika Olesova and Peter Mikus
Int. J. Mol. Sci. 2021, 22(15), 8261; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22158261 - 31 Jul 2021
Cited by 8 | Viewed by 2180
Abstract
In the presented study, a capillary electrophoresis-mass spectrometry method combining high separation efficiency and sensitive detection has been developed and validated, for the first time, to quantify branched chain amino acids (valine, isoleucine, leucine) in commercial food and sport supplement samples and human [...] Read more.
In the presented study, a capillary electrophoresis-mass spectrometry method combining high separation efficiency and sensitive detection has been developed and validated, for the first time, to quantify branched chain amino acids (valine, isoleucine, leucine) in commercial food and sport supplement samples and human plasma samples. The separations were performed in a bare fused silica capillary. The background electrolyte was composed of 500 mM formic acid with pH 2.0. The plasma sample pretreatment was realized by simple protein precipitation with acetonitrile. Injection of a short zone of highly basic electrolyte before the sample injection and application of the negative pressure on the separation were accompanied by enhanced resolution of the isobaric amino acids—isoleucine and leucine. The developed method was characterized by favorable validation parameters, such as linearity (r2 > 0.99), accuracy and precision, the limit of detection, lower limit of quantification, or robustness. These parameters were more than sufficient for the quantification of branched chain amino acids in various samples. The determined concentrations of branched chain amino acids in food and sports supplements were in very good agreement with the content declared by the manufacturer. The investigated concentrations of branched chain amino acids were in the range 294.68–359.24 µM for valine, 91.76–95.67 µM for isoleucine, and 196.78–251.24 µM for leucine. These concentrations fall within the physiological limits. The developed CE-MS/MS method represents a suitable alternative to traditional approaches used in branched chain amino acid quality control and bioanalysis. Full article
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14 pages, 1928 KiB  
Article
Electrophoretic Determination of Symmetric and Asymmetric Dimethylarginine in Human Blood Plasma with Whole Capillary Sample Injection
by Petr Tůma, Blanka Sommerová, Dušan Koval and François Couderc
Int. J. Mol. Sci. 2021, 22(6), 2970; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22062970 - 15 Mar 2021
Cited by 6 | Viewed by 1877
Abstract
Asymmetric and symmetric dimethylarginines are toxic non-coded amino acids. They are formed by post-translational modifications and play multifunctional roles in some human diseases. Their determination in human blood plasma is performed using capillary electrophoresis with contactless conductivity detection. The separations are performed in [...] Read more.
Asymmetric and symmetric dimethylarginines are toxic non-coded amino acids. They are formed by post-translational modifications and play multifunctional roles in some human diseases. Their determination in human blood plasma is performed using capillary electrophoresis with contactless conductivity detection. The separations are performed in a capillary covered with covalently bonded PAMAPTAC polymer, which generates anionic electroosmotic flow and the separation takes place in the counter-current regime. The background electrolyte is a 750 mM aqueous solution of acetic acid with pH 2.45. The plasma samples for analysis are treated by the addition of acetonitrile and injected into the capillary in a large volume, reaching 94.5% of the total volume of the capillary, and subsequently subjected to electrophoretic stacking. The attained LODs are 16 nm for ADMA and 22 nM for SDMA. The electrophoretic resolution of both isomers has a value of 5.3. The developed method is sufficiently sensitive for the determination of plasmatic levels of ADMA and SDMA. The determination does not require derivatization and the individual steps in the electrophoretic stacking are fully automated. The determined plasmatic levels for healthy individuals vary in the range 0.36–0.62 µM for ADMA and 0.32–0.70 µM for SDMA. Full article
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