Literature DB >> 23765673

An assay for α 1,6-fucosyltransferase (FUT8) activity based on the HPLC separation of a reaction product with fluorescence detection.

Hideyuki Ihara1, Hiroki Tsukamoto, Naoyuki Taniguchi, Yoshitaka Ikeda.   

Abstract

N-Glycans with an α-fucose unit linked to the 6-position of the innermost GlcNAc are widely distributed among the animal kingdom, from worms and insects to human. This α1,6-linked fucosyl residue, frequently referred to as a core fucose, is formed via the action of an α1,6-fucosyltransferase, the mammalian ortholog which is systematically called FUT8. In mammals, it is well known that the extent of core-fucosylation in cellular and secreted glycoproteins varies, e.g., according to differentiation and carcinogenesis of the cells. This chapter describes a method for the sensitive and quantitative assay of FUT8 activity using a fluorescence-labeled oligosaccharyl asparagine derivative as the glycosyl acceptor substrate.

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Year:  2013        PMID: 23765673     DOI: 10.1007/978-1-62703-465-4_25

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


  2 in total

1.  Shedding of N-acetylglucosaminyltransferase-V is regulated by maturity of cellular N-glycan.

Authors:  Tetsuya Hirata; Misaki Takata; Yuko Tokoro; Miyako Nakano; Yasuhiko Kizuka
Journal:  Commun Biol       Date:  2022-08-01

2.  Positive association of serum FUT8 activity with renal tubulointerstitial injury in IgA nephropathy patients.

Authors:  Ning Yang; Long-Kai Li; Hui He; Xia-Nan Guo; Xue-Feng Yuan; Zhi-Tong Li; Wei-Dong Wang; Biao-Jie Qin; Xiang-Ning Du; Xu Zhang; Shu-Ni Chen; Hong-Li Lin
Journal:  Immun Inflamm Dis       Date:  2022-09
  2 in total

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