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TbGT8 is a bifunctional glycosyltransferase that elaborates N-linked glycans on a protein phosphatase AcP115 and a GPI-anchor modifying glycan in Trypanosoma brucei

Authors :
Moe Karasudani
Mami Hino
Takahiro Shiraishi
Masayuki Nakanishi
Hiroshi Nomoto
Michael A. J. Ferguson
Kazunori Hashida
Source :
Parasitology International
Publisher :
The Authors. Published by Elsevier Ireland Ltd.

Abstract

The procyclic form of Trypanosoma brucei expresses procyclin surface glycoproteins with unusual glycosylphosphatidylinositol-anchor side chain structures that contain branched N-acetyllactosamine and lacto-N-biose units. The glycosyltransferase TbGT8 is involved in the synthesis of the branched side chain through its UDP-GlcNAc: βGal β1-3N-acetylglucosaminyltransferase activity. Here, we explored the role of TbGT8 in the mammalian bloodstream form of the parasite with a tetracycline-inducible conditional null T. brucei mutant for TbGT8. Under non-permissive conditions, the mutant showed significantly reduced binding to tomato lectin, which recognizes poly-N-acetyllactosamine-containing glycans. Lectin pull-down assays revealed differences between the wild type and TbGT8 null-mutant T. brucei, notably the absence of a broad protein band with an approximate molecular weight of 110 kDa in the mutant lysate. Proteomic analysis revealed that the band contained several glycoproteins, including the acidic ecto-protein phosphatase AcP115, a stage-specific glycoprotein in the bloodstream form of T. brucei. Western blotting with an anti-AcP115 antibody revealed that AcP115 was approximately 10 kDa smaller in the mutant. Enzymatic de-N-glycosylation demonstrated that the underlying protein cores were the same, suggesting that the 10-kDa difference was due to differences in N-linked glycans. Immunofluorescence microscopy revealed the colocalization of hemagglutinin epitope-tagged TbGT8 and the Golgi-associated protein GRASP. These data suggest that TbGT8 is involved in the construction of complex poly-N-acetyllactosamine-containing type N-linked and GPI-linked glycans in the Golgi of the bloodstream and procyclic parasite forms, respectively.<br />Graphical abstract<br />Highlights • TbGT8 is involved in N-linked glycan synthesis in the bloodstream form. • AcP115 is a target glycoprotein of TbGT8-dependent glycan processing. • TbGT8 is localized in the Golgi and modified by N-linked glycan(s).

Details

Language :
English
ISSN :
13835769
Issue :
3
Database :
OpenAIRE
Journal :
Parasitology International
Accession number :
edsair.doi.dedup.....f314836e5065c68ee903e94594421a4d
Full Text :
https://doi.org/10.1016/j.parint.2014.01.007