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Tandem lectin weak affinity chromatography for glycoprotein enrichment
Ma, Z.Y.
;
Skorobogatko, Y.
;
Vosseller, K.
Angol nyelvű Könyvfejezet (Könyvrészlet) Tudományos
Megjelent:
Jennifer J. Kohler. Mass Spectrometry of Glycoproteins. (2013) ISBN:9781627031455
pp. 21-31
Azonosítók
MTMT: 32618481
DOI:
10.1007/978-1-62703-146-2_2
Scopus:
84878639112
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.
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2025-04-27 18:02
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Hivatkozás stílusok:
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