Coupling of fully automated chip-based electrospray ionization to high-capacity ion trap mass spectrometer for ganglioside analysis

被引:61
作者
Almeida, Reinaldo [5 ]
Mosoarca, Cristina [1 ]
Chirita, Marius [1 ]
Udrescu, Valentina [1 ,2 ]
Dinca, Nicolae [3 ]
Vukelic, Zeljka [4 ]
Allen, Mark
Zamfir, Alina D. [1 ,3 ]
机构
[1] Natl Inst Res & Dev Electrochem & Condensed Matte, Mass Spectrometry Lab, Timisoara 300224, Romania
[2] Politehn Univ Timisoara, Fac Ind Chem & Environm Engn, Timisoara 300223, Romania
[3] Aurel Vlaicu Univ Arad, Dept Chem & Biol Sci, Arad 310130, Romania
[4] Univ Zagreb, Sch Med, Dept Chem & Biochem, Zagreb 10000, Croatia
[5] Advion Biosci, Norwich NR9 3DB, Norfolk, England
关键词
fully automated chip-nanoESI; high-capacity ion trap mass spectrometry; multistage CID; structural analysis; brain gangliosides; anencephaly;
D O I
10.1016/j.ab.2008.03.039
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
NanoMate robot was coupled to a high-capacity ion trap (HCT) mass spectrometer to create a system merging automatic chip-based electrospray ionization (ESI) infusion, ultrafast ion detection, and multistage sequencing at superior sensitivity. The interface between the NanoMate and HCT mass spectrometer consists of an in-laboratory constructed mounting device that allows adjustment of the robot position with respect to the mass spectrometer inlet. The coupling was optimized for ganglioside (GG) high-throughput analysis in the negative ion mode and was implemented in clinical glycolipidomics for identification and structural characterization of anencephaly-associated species. By NanoMate HCT mass spectrometry (MS), data corroborating significant differences in GG expression in anencephalic versus age-matched normal brain tissue were collected. The feasibility of chip-based nanoESI HCT multistage collision-induced dissociation (CID MSn) for polysialylated GG fragmentation and isomer discrimination was tested on a GT1 (d18:1/18:0) anencephaly-associated structure. MS2-MS4 obtained by accumulating scans at variable fragmentation amplitudes gave rise to the first fragmentation patterns from which the presence of GT1b structural isomer could be determined unequivocally without the need for supplementary investigation by any other analytical or biochemical methods. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:43 / 52
页数:10
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