Literature DB >> 20391534

2-picoline-borane: a non-toxic reducing agent for oligosaccharide labeling by reductive amination.

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.

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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


  40 in total

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9.  In-depth proteomic and glycomic analysis of the adult-stage Cooperia oncophora excretome/secretome.

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Review 10.  Structural glycomic analyses at high sensitivity: a decade of progress.

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