Hydrophilic interaction and reversed phase mixed-mode liquid chromatography coupled to high resolution tandem mass spectrometry for polar lipids analysis

被引:26
|
作者
Granafei, Sara [1 ]
Azzone, Pietro [1 ]
Spinelli, Vito Alessandro [1 ]
Losito, Ilario [1 ,2 ]
Palmisano, Francesco [1 ,2 ]
Cataldi, Tommaso R. I. [1 ,2 ]
机构
[1] Univ Bari Aldo Moro, Dipartimento Chim, Campus Univ,Via E Orabona 4, I-70126 Bari, Italy
[2] Univ Bari Aldo Moro, Ctr Ric Interdipartimentale SMART, Campus Univ,Via E Orabona 4, I-70126 Bari, Italy
关键词
Mixed-mode chromatography; Serially coupled columns; Phosholipids; Hydrophilic; Hydrophobic; Polar lipids; Tandem mass spectrometry; ELECTROSPRAY-IONIZATION; SHOTGUN LIPIDOMICS; SEPARATION; COLUMN; TRIACYLGLYCEROLS; IDENTIFICATION; PHOSPHATIDYLCHOLINES; FRAGMENTATION; PHOSPHOLIPIDS; OPTIMIZATION;
D O I
10.1016/j.chroma.2016.11.048
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A hydrophilic interaction liquid chromatography (HILIC) fused-core column (150 x 2.1 mm ID, 2.7 mu m particle size) and a short reversed-phase liquid chromatography (RPLC) column (20 mm x 2.1 mm ID, 1.9 mu m) were serially coupled to perform mixed-mode chromatography (MMC) on complex mixtures of phospholipids (PL). Mobile phase composition and gradient elution program were, preliminarily, optimized using a mixture of phosphatidylcholines (PC), phosphatidylethanolamines (PE), their corresponding lyso-forms (LPC and LPE), and sphingomyelins (SM). Thus a mixture of PC extracted from soybean was characterized by MMC coupled to electrospray ionization (ESI) high-resolution Fourier transform mass spectrometry (FTMS) using an orbital trap analyzer. Several previously undiscovered PC, including positional isomers (i.e. 16:0/19:1 and 19:1/16:0) of PC 35:1 and skeletal isomers (i.e. 18:1/18:2 and 18:0/18:3) of PC 36:3 were identified. Therefore, high-resolution MS/MS spectra unveiled the occurrence of isomers for several overall side chain compositions. The proposed MMC-ESI-FTMS/MS approach revealed an unprecedented capability in disclosing complexity of an actual lipid extract, thus representing a very promising approach to lipidomics. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:47 / 55
页数:9
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