A thin chip microsprayer system coupled to Fourier transform ion cyclotron resonance mass spectrometry for glycopeptide screening

被引:24
作者
Bindila, L
Froesch, M
Lions, N
Vukelic, Z
Rossier, JS
Girault, HH
Peter-Katalinic, J
Zamfir, AD
机构
[1] Univ Munster, Inst Med Phys & Biophys, D-48149 Munster, Germany
[2] Ecole Polytech Fed Lausanne, Lab Electrochim Phys & Analyt, CH-1015 Lausanne, Switzerland
[3] Univ Zagreb, Fac Med, Dept Chem & Biochem, Zagreb 10000, Croatia
[4] DiagnoSwiss SA, CH-1870 Monthey, Switzerland
关键词
D O I
10.1002/rcm.1705
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A thin polymer microchip was coupled with a Fourier transform ion cyclotron resonance (FTICR) 9.4 T mass spectrometer and the method was optimized in negative ion mode for glycopeptide screening. The interface between the polymer microchip and FTICR mass spectrometer consists of an in-laboratory conceived and designed mounting system that exhibits robust and controllable alignment of the chip toward the inlet of the mass spectrometer. The particular attribute of the polymer chip coupled to the FTICR mass spectrometer, to achieve an increase in ionization efficiency and sensitivity under the premise of high mass accuracy of detection, is highlighted by the large number of major and minor glycopeptide structures detected and identified in highly heterogeneous mixtures obtained from urine matrices. Glycoforms expressing various saccharide chain lengths ranging from tri- to dodecasaccharide, bearing up to three sialic acid moieties, could be detected and assigned based on the accuracy of the mass measurement (average mass deviation below 6 ppm) of their molecular ions. (-)Thin chipESI-FTICRMS is a potent novel system for glycomic screening of complex mixtures, as demonstrated for identification of singly sialylated O-glycosylated amino acids and peptides from urine matrices, and could be considered for general applicability in the glycoanalytical field. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:2913 / 2920
页数:8
相关论文
共 46 条
[1]   Off-line capillary electrophoresis/fully automated nanoelectrospray chip quadrupole time-of-flight mass spectrometry and tandem mass spectrometry for glycoconjugate analysis [J].
Bindila, L ;
Almeida, R ;
Sterling, A ;
Allen, M ;
Peter-Katalinic, J ;
Zamfir, A .
JOURNAL OF MASS SPECTROMETRY, 2004, 39 (10) :1190-1201
[2]  
DAYON L, 2004, IN PRESS ELECTROPHOR
[3]   Atomic weights of the elements:: Review 2000 -: (IUPAC technical report) [J].
De Laeter, JR ;
Böhlke, JK ;
De Bièvre, P ;
Hidaka, H ;
Peiser, HS ;
Rosman, KJR ;
Taylor, PDP .
PURE AND APPLIED CHEMISTRY, 2003, 75 (06) :683-800
[4]   ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY WITH MILD CLINICAL MANIFESTATIONS AND DIFFICULT BIOCHEMICAL-DIAGNOSIS [J].
DEJONG, J ;
VANDENBERG, C ;
WIJBURG, H ;
WILLEMSEN, R ;
VANDIGGELEN, O ;
SCHINDLER, D ;
HOEVENAARS, F ;
WEVERS, R .
JOURNAL OF PEDIATRICS, 1994, 125 (03) :385-391
[5]   Chip-based capillary electrophoresis/mass spectrometry determination of carnitines in human urine [J].
Deng, YZ ;
Henion, J ;
Li, JJ ;
Thibault, P ;
Wang, C ;
Harrison, DJ .
ANALYTICAL CHEMISTRY, 2001, 73 (03) :639-646
[6]   Chip-based quantitative capillary electrophoresis/mass spectrometry determination of drugs in human plasma [J].
Deng, YZ ;
Zhang, NW ;
Henion, J .
ANALYTICAL CHEMISTRY, 2001, 73 (07) :1432-1439
[7]  
DESNICK RJ, 2001, METABOLIC MOL BASES, P3483
[8]   Demonstration of direct bioanalysis of drugs in plasma using nanoelectrospray infusion from a silicon chip coupled with tandem mass spectrometry [J].
Dethy, JM ;
Ackermann, BL ;
Delatour, C ;
Henion, JD ;
Schultz, GA .
ANALYTICAL CHEMISTRY, 2003, 75 (04) :805-811
[9]   Sialylation analysis of O-glycosylated sialylated peptides from urine of patients suffering from Schindler's disease by Fourier transform ion cyclotron resonance mass spectrometry and sustained off-resonance irradiation collision-induced dissociation [J].
Froesch, M ;
Bindila, L ;
Zamfir, A ;
Peter-Katalinic, J .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2003, 17 (24) :2822-2832
[10]  
Gobry V, 2002, PROTEOMICS, V2, P405, DOI 10.1002/1615-9861(200204)2:4<405::AID-PROT405>3.0.CO