4.7 Article

Studying O-linked protein glycosylations in human plasma

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 7, Issue 6, Pages 2562-2568

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/pr800066e

Keywords

protein O-glycosylations; plasma; epithelial ovarian cancer (EOC); matrix-assisted laser desorption/iozation (MALDI); Fourier transform-ion cyclotron resonance mass spectrometry (FT-ICR-MS)

Funding

  1. NATIONAL CANCER INSTITUTE [R33CA105295] Funding Source: NIH RePORTER
  2. NCI NIH HHS [R33 CA105295] Funding Source: Medline

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Recent investigations have implicated aberrant glycosylations in various malignancies, including epithelial ovarian cancer (EOC). The protocol here identifies O-linked carbohydrate patterns in EOC plasma glycoproteins through chemical cleavage and purification of these glycans. Dialyzed plasma is subjected to reductive beta-elimination with alkaline borohydride to release O-linked oligosaccharides from glycoproteins. Enrichment of released glycans, as well as removal of peptide and other contaminants, is followed by carbohydrate pattern analysis with MALDI-FT-ICR-MS.

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