Cite as: Cold Spring Harb. Protoc.; 2006; doi:10.1101/pdb.prot4247
| Protocol |
This protocol was adapted from "Monosaccharide Analysis by Methanolysis," contributed by David Oxley, Graeme Currie, and Antony Bacic, Chapter 25, in Purifying Proteins for Proteomics (ed. Simpson). Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA, 2004.
| The first 15% of the full text of this article appears below. |
INTRODUCTION
Methanolysis allows rapid determination of monosaccharide composition of glycans, glycoproteins, and proteoglycans by cleaving glycosidic bonds to produce methyl glycosides. The free-hydroxyl groups on the glycosides are derivatized with trimethylsilyl (TMS) groups to make the compounds volatile before they are analyzed by gas chromatography (GC) or gas chromatography coupled with mass spectrometry (GC-MS). The method gives more complex chromatograms than the corresponding alditol acetate method (see Monosaccharide Composition Analysis: Alditol Acetates), because up to four methyl glycosides can be produced from each monosaccharide. However, the method is easier to perform.
MATERIALS
Reagents
Acetic anhydride
t-Butyl alcohol
Equipment
METHOD
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