Characterization of DESI-FTICR mass spectrometry - from ECD to accurate mass tissue analysis

被引:18
作者
Takats, Zoltan [2 ]
Kobliha, Vaclav [1 ]
Sevcik, Karel [1 ]
Novak, Petr [1 ]
Kruppa, Gary [3 ]
Lemr, Karel [4 ]
Havlicek, Vladimir [1 ]
机构
[1] Acad Sci Czech Republ, Inst Microbiol, CR-14220 Prague 4, Czech Republic
[2] Semmelweis Univ, H-1085 Budapest, Hungary
[3] Bruker Daltonics Inc, Fremont, CA 94538 USA
[4] Palacky Univ, Dept Analyt Chem, Olomouc 77146, Czech Republic
来源
JOURNAL OF MASS SPECTROMETRY | 2008年 / 43卷 / 02期
关键词
desorption electrospray; ion cyclotron resonance; lipids; electron capture dissociation; peptides;
D O I
10.1002/jms.1285
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Implementation of desorption electrospray ionization (DESI) technique on a 9.4 T Fourier transform ion cyclotron resonance ITTICR) mass spectrometer is described. Desorption electrospray technique is capable of the direct investigation of natural samples without any need for sample preparation or chromatographic separation. Since the DESI mass spectra of natural samples are very complex owing to the lack of preseparation or cleanup, the ideal mass spectrometric analyzer for these applications is a high-resolution instrument such as FTICR mass spectrometer. DESI was implemented by constructing an electronically controlled source framework comprising six linear moving stages and one rotating stage. A three-dimensional linear stage was used to accommodate samples, while another 3D linear stage equipped with rotating stage was used as a spray mount. A modified electrosonic sprayer was used as a primary electrospray device. DESI-FTICR setup was characterized with regard to geometrical, electrical and flow conditions using deposited peptide samples in range of 1-100 pmol gross deposited amount on glass and polymer surfaces. Optimized conditions enabled the routine acquisition of DESI-MS spectra on the instrument at 130 000 resolution in the broadband mode and with comparable sensitivity to data reported in the literature. Since the main significance of DESI-FTICR MS is the combination of intact tissue analysis, the capabilities of the technique were demonstrated by analyzing murine liver samples. Presence of lysophospholipids in the liver tissue was tentatively associated with the lipid metabolism taking place in liver. DESI-FTICR is also a promising technique in the field of peptide analysis due to capability of top-down sequencing using electron capture dissociation. As a proof-of-principle experiment, a small synthetic polypeptide containing 36 amino acids was ionized using DESI and was sequenced in the FTICR by means of ECD (electron capture dissociation) fragmentation. Spectra gave almost full sequence information in agreement with the known amino acid sequence of the species. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:196 / 203
页数:8
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