| Literature DB >> 20391534 |
L Renee Ruhaak1, Evelyne Steenvoorden, Carolien A M Koeleman, André M Deelder, Manfred Wuhrer.
Abstract
Analysis of N-glycans is often performed by LC coupled to fluorescence detection. The N-glycans are usually labeled by reductive amination with a fluorophore containing a primary amine to allow fluorescence detection. Moreover, many of the commonly applied labels also allow improved mass spectrometric detection of oligosaccharides. For reductive amination, the amine group of the label reacts with the reducing-end aldehyde group of the oligosaccharide to form a Schiff base, which is reduced to a secondary amine. Here, we propose the use of 2-picoline-borane as the reducing agent, as a non-toxic alternative to the extensively used, but toxic sodium cyanoborohydride. Using dextran oligosaccharides and plasma N-glycans, we demonstrate similar labeling efficacies for 2-picoline-borane and sodium cyanoborohydride. Therefore, 2-picoline-borane is a non-toxic alternative to sodium cyanoborohydride for the labeling of oligosaccharides.Entities:
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Year: 2010 PMID: 20391534 DOI: 10.1002/pmic.200900804
Source DB: PubMed Journal: Proteomics ISSN: 1615-9853 Impact factor: 3.984