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Different O-glycosylation of respiratory mucin glycopeptides from a patient with cystic fibrosis.

Artikel i vetenskaplig tidskrift
Författare Kristina A Thomsson
I Carlstedt
Niclas G. Karlsson
Hasse Karlsson
Gunnar C. Hansson
Publicerad i Glycoconjugate journal
Volym 15
Nummer/häfte 8
Sidor 823-33
ISSN 0282-0080
Publiceringsår 1998
Publicerad vid Institutionen för medicinsk och fysiologisk kemi
Sidor 823-33
Språk en
Länkar www.ncbi.nlm.nih.gov/entrez/query.f...
Ämnesord Adolescent, Carbohydrate Sequence, Chromatography, High Pressure Liquid, Cystic Fibrosis, Female, Gas Chromatography-Mass Spectrometry, Glycopeptides, chemistry, Glycosylation, Humans, Molecular Sequence Data, Mucins, chemistry, Oligosaccharides, chemistry, Sequence Analysis, Spectrometry, Mass, Fast Atom Bombardment, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Sputum, chemistry, Sulfuric Acid Esters
Ämneskategorier Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi), molekylärbiologi, mikrobiologi, biokemi eller biofarmaci)

Sammanfattning

The O-linked oligosaccharides from three fractions of highly glycosylated mucin glycopeptides obtained from sputum of a patient with cystic fibrosis were characterized and compared regarding size, composition, sequence and when possible linkage positions. Neutral and sialic acid-containing glycans were permethylated and analyzed by high-temperature GC-MS and MALDI-MS, showing more than 60 different oligosaccharides with a size of up to 15 monosaccharide units. Some of the observed oligosaccharides are novel for respiratory secretions, one being a trifucosylated heptasaccharide with the proposed structure: Fuc-Gal-4(Fuc-3)GlcNAc-(Fuc-)Gal-3GalNAcol. The glycosylation of two of the glycopeptide fractions was similar with regard to the neutral and sialylated oligosaccharides despite their different origins from the sol or gel phase. Analysis of the sulfated oligosaccharides by FAB-MS/MS indicated that the gel fraction contained C-6 linked sulfate groups while the two sol fractions also contained C-3 linked sulfate. The results suggest the presence of different glycosylated mucin domains, probably originating from different mucin glycoforms and/or apoproteins in the airway of cystic fibrosis patients.

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