Literature DB >> 21604131

Strong cation exchange chromatography for analysis of sialylated glycopeptides.

Katharina Lohrig1, Albert Sickmann, Urs Lewandrowski.   

Abstract

Glycosylations represent major and essential co- and post-translational modification forms of proteins and facilitate a multitude of functions such as cell-cell interactions as well as protein folding and stability. The analysis of protein glycosylation is still an enormous task due to the vast heterogeneity and multitude of different possible carbohydrate structures. The elucidation of glycosylation sites - the attachment points of carbohydrate structures to the polypeptide backbone - is often among the first necessary steps of analysis. Therefore, we here present a simple protocol for charge-based enrichment of sialylated glycopeptides by strong cation exchange chromatography and subsequent analysis of glycosylation sites by mass spectrometry.

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Year:  2011        PMID: 21604131     DOI: 10.1007/978-1-61779-148-2_20

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

Review 1.  Current strategies and findings in clinically relevant post-translational modification-specific proteomics.

Authors:  Oliver Pagel; Stefan Loroch; Albert Sickmann; René P Zahedi
Journal:  Expert Rev Proteomics       Date:  2015-05-08       Impact factor: 3.940

  1 in total

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