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Predictive Liquid Chromatography of Peptides Based on Hydrophilic Interactions for Mass Spectrometry-Based Proteomics

Authors :
Lobas, A.A.
Levitsky, L.I.
Fichtenbaum, A.
Surin, A.K.
Pridatchenko, M.L.
Mitulovic, G.
Gorshkov, A.V.
Gorshkov, M.V.
Source :
Journal of Analytical Chemistry. December 30, 2017, Vol. 72 Issue 14, p1375, 8 p.
Publication Year :
2017

Abstract

High-performance liquid chromatography (HPLC) is widely used for separation of complex peptide mixtures before mass spectrometry-based proteome analysis. In this analysis, reversed phase HPLC (RPHPLC) using non-polar stationary phases such as surface-modified silica containing alkyl groups (e.g., C18) is typically employed. Because of the high heterogeneity of proteomic samples, multidimensional separation approaches gained increasing attention recently to tackle this complexity and extremely high range of concentrations. In two-dimensional liquid chromatography, hydrophilic interaction chromatography (HILIC) is often a method of choice for combination with RP-HPLC because it uses reversed-phase type eluents and allows efficient separation of polar peptides. Due to the high degree of orthogonality in this two-dimensional separation space, it is tempting to develop approaches for predicting peptide retention times for HILIC-based separations similar to the ones for RP-HPLC. Recent successful efforts in this area were focused on developing retention coefficient (RC)-based approaches. Herein, we explored the feasibility of using a statistical thermodynamic model for prediction of peptide retention times in HILIC separations and determined the phenomenological parameters of the model for a bare silica column. The performance of the developed model was tested using HPLC-MS analysis of a set of synthetic peptides, as well as a tryptic peptide mixture. Keywords: HILIC, peptide separation, proteomics, retention time prediction DOI: 10.1134/S1061934817140076<br />INTRODUCTION Proteomics is a general term for a variety of approaches and techniques used for large-scale identification and quantification of proteins present in certain cell, tissue, or body fluid of [...]

Details

Language :
English
ISSN :
10619348
Volume :
72
Issue :
14
Database :
Gale General OneFile
Journal :
Journal of Analytical Chemistry
Publication Type :
Academic Journal
Accession number :
edsgcl.532654863
Full Text :
https://doi.org/10.1134/S1061934817140076