Structural Analysis of N-Glycans by the Glycan-Labeling Method Using 3-Aminoquinoline-Based Liquid Matrix in Negative-Ion MALDI-MS

2012 ◽  
Vol 84 (21) ◽  
pp. 9453-9461 ◽  
Author(s):  
Takashi Nishikaze ◽  
Kaoru Kaneshiro ◽  
Shin-ichirou Kawabata ◽  
Koichi Tanaka
2017 ◽  
Vol 41 (20) ◽  
pp. 12241-12249 ◽  
Author(s):  
Ling Ling ◽  
Chunsheng Xiao ◽  
Liyan Jiang ◽  
Sheng Wang ◽  
Ying Li ◽  
...  

An optimized ILM G3THAP/PA matrix significantly improved the detection of phosphopeptides by negative ion MALDI-MS compared with using 3-AQ/CHCA/ADP and DHB/PA matrices.


2005 ◽  
Vol 77 (18) ◽  
pp. 6062-6068 ◽  
Author(s):  
Yasuhiro Takegawa ◽  
Kisaburo Deguchi ◽  
Hiroaki Nakagawa ◽  
Shin-Ichiro Nishimura

2011 ◽  
Vol 83 (10) ◽  
pp. 3663-3667 ◽  
Author(s):  
Kaoru Kaneshiro ◽  
Yuko Fukuyama ◽  
Shinichi Iwamoto ◽  
Sadanori Sekiya ◽  
Koichi Tanaka

2018 ◽  
Vol 10 (6) ◽  
pp. 572-578 ◽  
Author(s):  
Jinlan Dong ◽  
Wenjing Ning ◽  
Daniel J. Mans ◽  
Jamie D. Mans

A mixture of α-cyano-4-hydroxycinnamic acid and 1,5-diaminonaphthalene was discovered as a novel binary matrix for the qualitative analysis of 14 small-molecule (∼250–550 Da) cardiovascular drugs by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) and MS/MS in either positive or negative ion mode.


2012 ◽  
Vol 23 (11) ◽  
pp. 1955-1966 ◽  
Author(s):  
David J. Harvey ◽  
Charlotte A. Scarff ◽  
Max Crispin ◽  
Christopher N. Scanlan ◽  
Camille Bonomelli ◽  
...  

2013 ◽  
Vol 85 (19) ◽  
pp. 9156-9163 ◽  
Author(s):  
Annabelle Fülöp ◽  
Martina B. Porada ◽  
Christian Marsching ◽  
Henning Blott ◽  
Björn Meyer ◽  
...  

1971 ◽  
Vol 54 (6) ◽  
pp. 1340-1348 ◽  
Author(s):  
Peter C Rankin

Abstract A study of the negative ion mass spectra of a number of complex organic molecules (pesticides) was undertaken to determine what information this technique would yield for structural analysis. The simplicity of the negative ion mass spectra was a characteristic feature and the most abundant negative ions in the spectra were assumed to be similar to the stable carbanions postulated in classical organic chemistry. The simplicity of the mass spectra suggested a possible application of the technique to the identification of carbamate pesticides.


2020 ◽  
Vol 16 (1) ◽  
pp. 79-91
Author(s):  
Kathrin M. Engel ◽  
Ulrike Jakop ◽  
Karin Müller ◽  
Sonja Grunewald ◽  
Uwe Paasch ◽  
...  

Background: The sperm plasma membrane meets the requirements of sperm transit through the female genital tract and subsequent fertilization. Commonly, the (phospho)lipid composition of sperm is characterized by tremendous amounts of highly unsaturated fatty acyl residues such as docosahexaenoic and docosapentaenoic acid. While human sperm contain almost exclusively diacyl lipids, many animal sperm additionally contain significant amounts of ether lipids such as alkylacyl- and alkenyl-acyl lipids (plasmalogens). Hypothesis/Objective: It is suggested that deviations from the typical lipid composition are indicative of pathological changes. Therefore, simple methods to elucidate the sperm lipid composition are essential. Method: Matrix-assisted laser desorption and ionization (MALDI) mass spectrometry (MS) is a fast and simple method. Since the selection of the most suitable matrix is a crucial step in MALDI MS, this topic will be highlighted. It will also be shown that MALDI MS can be easily combined with thin-layer chromatography to overcome ion suppression effects. Results: The lipid composition of sperm from different species can be elucidated by MALDI MS. However, different matrix compounds have to be used to record positive and negative ion mass spectra. Since some sperm (glyco)lipids are characterized by the presence of sulfate residues which suppress the detection of less acidic lipids in the negative ion mode, previous separation is often necessary. It will be also emphasized that plasmalogens can be easily identified by either enzymatic digestion or treatment with acids. Conclusion: MALDI MS is a reliable method to obtain sperm lipid fingerprints in a simple and convenient way.


ChemInform ◽  
2001 ◽  
Vol 32 (11) ◽  
pp. no-no
Author(s):  
Anne Dell ◽  
Howard R. Morris ◽  
Richard Easton ◽  
Stuart Haslam ◽  
Maria Panico ◽  
...  
Keyword(s):  

2004 ◽  
Vol 18 (2) ◽  
pp. 185-201 ◽  
Author(s):  
Warren C. Kett ◽  
Deirdre R. Coombe

Mass spectrometry (MS) techniques have spear‒headed the field of proteomics. Recently, MS has been used to structurally analyse carbohydrates. The heparin/heparan sulfate‒like glycosaminoglycans (HLGAGs) present a special set of difficulties for structural analysis because they are highly sulfated and heterogeneous. We have used a matrix‒assisted laser desorption/ionization time of flight mass spectrometry (MALDI‒MS) technique in which heparin fragments are non‒covalently bound to basic peptides of a known mass, so as to limit in‒source desulfation and hence afford an accurate mass. We examined a range of different sized fragments with varying degrees of sulfation. The potential of combining the MALDI‒MS technique with enzymatic digestion to obtain saccharide sequence information on heparin fragments was explored. A disaccharide analysis greatly assists in determining a sequence from MALDI‒MS data. Enzymatic digestion followed by MALDI‒MS allows structural data on heparin fragments too large for direct MALDI‒MS to be obtained. We demonstrate that synthetic sulfated oligosaccharides can also be analysed by MALDI‒MS. There are advantages and limitations with this methodology, but until superior MS techniques become readily accessible to biomedical scientists the MALDI‒MS method provides a means to structurally analyse HLGAG fragments that have therapeutic potential because of their ability to bind to and functionally regulate a host of clinically important proteins.


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