Improved Liquid Chromatography-MS/MS of Heparan Sulfate Oligosaccharides via Chip-Based Pulsed Makeup Flow

被引:34
作者
Huang, Yu [1 ]
Shi, Xiaofeng [1 ]
Yu, Xiang [1 ]
Leymarie, Nancy [1 ]
Staples, Gregory O. [2 ]
Yin, Hongfeng [2 ]
Killeen, Kevin [2 ]
Zaia, Joseph [1 ]
机构
[1] Boston Univ, Sch Med, Dept Biochem, Ctr Biomed Mass Spectrometry, Boston, MA 02118 USA
[2] Agilent Labs, Santa Clara, CA 95051 USA
关键词
TANDEM MASS-SPECTROMETRY; ELECTRON DETACHMENT DISSOCIATION; MOLECULAR DIVERSITY; DISACCHARIDES; CHARGE; MECHANISMS; GLYCOMICS;
D O I
10.1021/ac201964n
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Microfluidic chip-based hydrophilic interaction chromatography (HILIC) is a useful separation system for liquid chromatography-mass spectrometry (LC-MS) in compositional profiling of heparan sulfate (HS) oligosaccharides; however, ions observed using HILIC LC-MS are low in charge. Tandem MS of HS oligosaccharide ions with low charge results in undesirable losses of SO3 from precursor ions during collision induced dissociation. One solution is to add metal cations to stabilize sulfate groups. Another is to add a nonvolatile, polar compound such as sulfolane, a molecule known to supercharge proteins, to produce a similar effect for oligosaccharides. We demonstrate use of a novel pulsed makeup flow (MUF) HPLC-chip. The chip enables controlled application of additives during specified chromatographic time windows and thus minimizes the extent to which nonvolatile additives build up in the ion source. The pulsed MUF system was applied to LC-MS/MS of HS oligosaccharides. Metal cations and sulfolane were tested as additives. The most promising results were obtained for sulfolane, for which supercharging of the oligosaccharide ions increased their signal strengths relative to controls. Tandem MS of these supercharged precursor ions showed decreased abundances of product ions from sulfate losses yet more abundant product ions from backbone cleavages.
引用
收藏
页码:8222 / 8229
页数:8
相关论文
共 38 条
[1]   Modular Synthesis of Heparan Sulfate Oligosaccharides for Structure-Activity Relationship Studies [J].
Arungundram, Sailaja ;
Al-Mafraji, Kanar ;
Asong, Jinkeng ;
Leach, Franklin E., III ;
Amster, I. Jonathan ;
Venot, Andre ;
Turnbull, Jeremy E. ;
Boons, Geert-Jan .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (47) :17394-17405
[2]   The molecular diversity of glycosaminoglycans shapes animal development [J].
Bulow, Hannes E. ;
Hobert, Oliver .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2006, 22 :375-407
[3]   Molecular diversity of heparan sulfate [J].
Esko, JD ;
Lindahl, U .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (02) :169-173
[4]   DIFFERENTIATION OF CA2+-COORDINATED AND MG2+-COORDINATED BRANCHED TRISACCHARIDE ISOMERS - AN ELECTROSPRAY-IONIZATION AND TANDEM MASS-SPECTROMETRY STUDY [J].
FURA, A ;
LEARY, JA .
ANALYTICAL CHEMISTRY, 1993, 65 (20) :2805-2811
[5]   Optimized extraction of glycosaminoglycans from normal and osteoarthritic cartilage for glycomics profiling [J].
Hitchcock, Alicia M. ;
Yates, Karen E. ;
Shortkroff, Sonya ;
Costello, Catherine E. ;
Zaia, Joseph .
GLYCOBIOLOGY, 2007, 17 (01) :25-35
[6]   Comparative glycomics of connective tissue glycosaminoglycans [J].
Hitchcock, Alicia M. ;
Yates, Karen E. ;
Costello, Catherine E. ;
Zaia, Joseph .
PROTEOMICS, 2008, 8 (07) :1384-1397
[7]   Glycoform quantification of chondroitin/dermatan sulfate using a liquid chromatography-tandem mass spectrometry platform [J].
Hitchcock, AM ;
Costello, CE ;
Zaia, J .
BIOCHEMISTRY, 2006, 45 (07) :2350-2361
[8]   LINKAGE POSITION DETERMINATION IN LITHIUM-CATIONIZED DISACCHARIDES - TANDEM MASS-SPECTROMETRY AND SEMIEMPIRICAL CALCULATIONS [J].
HOFMEISTER, GE ;
ZHOU, Z ;
LEARY, JA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (16) :5964-5970
[9]  
Huang R, 2011, J AM SOC MASS SPECTR, P1
[10]   Recent progress and applications in glycosaminoglycan and heparin research [J].
Laremore, Tatiana N. ;
Zhang, Fuming ;
Dordick, Jonathan S. ;
Liu, Jian ;
Linhardt, Robert J. .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2009, 13 (5-6) :633-640