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High reproducibility of two-dimensional liquid chromatography using pH-driven fractionation with a pressure-resistant electrode

Authors :
Daniel Gonzalez-Dunia
Frédéric Pont
Elsa Suberbielle
Centre de Physiopathologie Toulouse Purpan (CPTP)
Université Toulouse III - Paul Sabatier (UT3)
Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Plateau Technique de Spectrométrie de Masse
Institut Claude de Préval (ICP)
Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Toulouse [Toulouse]-Université Toulouse III - Paul Sabatier (UT3)
Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Toulouse [Toulouse]-Université Toulouse III - Paul Sabatier (UT3)
Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées
Source :
Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences, Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences, Elsevier, 2008, 871 (1), pp.125-9. ⟨10.1016/j.jchromb.2008.06.043⟩
Publication Year :
2008
Publisher :
HAL CCSD, 2008.

Abstract

International audience; Automated two-dimensional liquid chromatography using the PF2D system from Beckman Coulter provides a fractionation platform well suited for differential proteomic studies. To date, the reliability and reproducibility of PF2D has not been accurately tested. Here, we used an optimized software and a pressure-resistant pH electrode, allowing a precise and reproducible control of the pH limits for each fraction during PF2D. We tested the reliability of this improved system by performing several rounds of fractionation using the same protein extract. Three UV maps were generated, leading to 54 chromatograms and more than 3000 protein peaks. Using semi-automated software for peak-to-peak comparison between 2D-LC chromatograms, we demonstrate that the peak concordance is very high. The rates of concordance were higher in the second dimension repeatability tests, indicating that the limiting factors for 2D-LC reproducibility rely on the pI fractionation and sample preparation steps. The reproducibility between maps was closely related to pH curves similarities, further stressing the need of careful pH adjustment and precise electrode calibration.

Details

Language :
English
ISSN :
15700232 and 1873376X
Database :
OpenAIRE
Journal :
Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences, Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences, Elsevier, 2008, 871 (1), pp.125-9. ⟨10.1016/j.jchromb.2008.06.043⟩
Accession number :
edsair.doi.dedup.....ef89363fe5b7b9e9417e8f09a5f3b56d
Full Text :
https://doi.org/10.1016/j.jchromb.2008.06.043⟩