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PMID: 17223647 Published · ppublish English Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Comparison of the methods for profiling glycoprotein glycans--HUPO Human Disease Glycomics/Proteome Initiative multi-institutional study.

Glycobiology ·Vol. 17 ·No. 4 ·2007-04-00 ·Pages 411-22

Wada Y, Azadi P, Costello CE, Dell A, Dwek RA, Geyer H, Geyer R, Kakehi K, Karlsson NG, Kato K, Kawasaki N, Khoo KH, Kim S, Kondo A, Lattova E, Mechref Y, Miyoshi E, Nakamura K, Narimatsu H, Novotny MV, Packer NH, Perreault H, Peter-Katalinic J, Pohlentz G, Reinhold VN, Rudd PM, Suzuki A, Taniguchi N

Abstract

Mass spectrometry (MS) of glycoproteins is an emerging field in proteomics, poised to meet the technical demand for elucidation of the structural complexity and functions of the oligosaccharide components of molecules. Considering the divergence of the mass spectrometric methods employed for oligosaccharide analysis in recent publications, it is necessary to establish technical standards and demonstrate capabilities. In the present study of the Human Proteome Organisation (HUPO) Human Disease Glycomics/Proteome Initiative (HGPI), the same samples of transferrin and immunoglobulin-G were analyzed for N-linked oligosaccharides and their relative abundances in 20 laboratories, and the chromatographic and mass spectrometric analysis results were evaluated. In general, matrix-assisted laser desorption/ionization (MALDI) time-of-flight MS of permethylated oligosaccharide mixtures carried out in six laboratories yielded good quantitation, and the results can be correlated to those of chromatography of reductive amination derivatives. For underivatized oligosaccharide alditols, graphitized carbon-liquid chromatography (LC)/electrospray ionization (ESI) MS detecting deprotonated molecules in the negative ion mode provided acceptable quantitation. The variance of the results among these three methods was small. Detailed analyses of tryptic glycopeptides employing either nano LC/ESI MS/MS or MALDI MS demonstrated excellent capability to determine site-specific or subclass-specific glycan profiles in these samples. Taking into account the variety of MS technologies and options for distinct protocols used in this study, the results of this multi-institutional study indicate that MS-based analysis appears as the efficient method for identification and quantitation of oligosaccharides in glycomic studies and endorse the power of MS for glycopeptide characterization with high sensitivity in proteomic programs.

MeSH Terms
Carbohydrate Conformation Gene Expression Profiling/methods Genetic Diseases, Inborn/genetics Glycopeptides/chemistry Glycoproteins/chemistry,genetics Humans Mass Spectrometry Models, Molecular Oligosaccharides/chemistry Polysaccharides/chemistry,genetics Proteome Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Chemicals
Glycopeptides Glycoproteins Oligosaccharides Polysaccharides Proteome
Authors & Affiliations
28 authors, click to expand affiliations / ORCID
Wada Yoshinao
Osaka Medical Center and Research Institute for Maternal and Child Health, 840 Murodo-cho, Izumi, Osaka 594-1101, Japan. [email protected]
Azadi Parastoo
Costello Catherine E
Dell Anne
Dwek Raymond A
Geyer Hildegard
Geyer Rudolf
Kakehi Kazuaki
Karlsson Niclas G
Kato Koichi
Kawasaki Nana
Khoo Kay-Hooi
Kim Soohyun
Kondo Akihiro
Lattova Erika
Mechref Yehia
Miyoshi Eiji
Nakamura Kazuyuki
Narimatsu Hisashi
Novotny Milos V
Packer Nicolle H
Perreault Hélène
Peter-Katalinic Jasna
Pohlentz Gottfried
Reinhold Vernon N
Rudd Pauline M
Suzuki Akemi
Taniguchi Naoyuki
Article Info
Journal
Glycobiology
Abbr.
Glycobiology
ISSN
0959-6658
Published
2007-04-00
Epub
2007-00-12
Pages
411-22
Language
English
Region
England
NLM ID
9104124
Subset
IM
Corrections
ErratumIn
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