1. Academic Validation
  2. Fucosylation of complex glycosphingolipids by recombinant fucosyltransferase-VII

Fucosylation of complex glycosphingolipids by recombinant fucosyltransferase-VII

  • Biochem Biophys Res Commun. 1997 Sep 8;238(1):165-8. doi: 10.1006/bbrc.1997.7254.
M R Stroud 1 E H Holmes
Affiliations

Affiliation

  • 1 Department of Cell Surface Biochemistry, Northwest Hospital, Seattle, Washington 98125, USA.
Abstract

Fucosyltransferase VII (FucT-VII) is one of five known alpha 1-->3fucosyltransferases capable of transferring fucose to the C-3 position of N-acetylglucosamine residues found in lactosamine based glycans. Previous studies have indicated that FucT-VII has a very restricted specificity, capable of fucosylating only terminally alpha 2-->3sialylated carbohydrate substrates, resulting in the synthesis of the sialyl Lewis x (sLe(x)) epitope. Although FucT-VII is expressed in cells of myeloid origin, the monosialylganglioside fraction of HL60 cells contains only internally and/or multiply fucosylated polylactosamine structures; no monofucosylated sLe(x) derivatives are detected. We now report that the structure of the final product formed by the action of FucT-VII on sialynorhexaosylceramide (a glycosphingolipid substrate having multiple fucosylation sites) is extended monofucosyl sLe(x) and fucosylation is restricted to the terminal GlcNAc-V. This indicates that the biosynthesis of all fucosylated monosialylated gangliosides found in HL60 cells (including the E-Selectin binding fractions) involves at least one additional alpha 1-->3fucosyltransferase.

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