In this chapter we describe the application of lectin weak Affinity chromatography (LWAC) for the enrichment of peptides modified by O-linked β - N -acetylglucosamine (O-GlcNAc). O-GlcNAc is a single carbohydrate moiety post-translational modification of intracellular proteins. The stoichiometry of the modification is low and identification of the sites of O-GlcNAc attachment is challenging. To map O-GlcNAc sites we use the approach where a protein sample of interest is digested with trypsin and subjected to LWAC, which employs weak interaction between lectin wheat germ agglutinin and O-GlcNAc. Obtained sample is enriched with O-GlcNAc-modified peptides, which can be identified by means of mass spectrometry. © Springer Science+Business Media, LLC 2013.
CITATION STYLE
Ma, Z. Y., Skorobogatko, Y., & Vosseller, K. (2013). Tandem lectin weak affinity chromatography for glycoprotein enrichment. Methods in Molecular Biology, 951, 21–31. https://doi.org/10.1007/978-1-62703-146-2_2
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