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Continuous nonradioactive method for screening trypanosomal transsialidase activity and its inhibitors
- Source :
- Glycobiology 2010;20(8):982-990, Biblioteca Digital (UBA-FCEN), Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales, instacron:UBA-FCEN
- Publication Year :
- 2010
-
Abstract
- Trypanosoma cruzi, the agent of American trypanosomiasis is unable to synthesize sialic acid (SA). Instead of using the corresponding nucleotide sugar as donor of the monosaccharide, the transfer occurs from α-2,3-linked SA in the host sialoglycoconjugates to terminal β-galactopyranosyl units of the parasite mucins. For that purpose, T. cruzi expresses a glycosylphosphatidylinositol-anchored transsialidase (TcTS) that is shed into the milieu, being detected in the blood during the acute phase of the infection. The essential role of TcTS in infection and the absence of a similar activity in mammals make this enzyme an attractive target for the development of alternative chemotherapies. However, there is no effective inhibitor toward this enzyme. In vitro, 3′-sialyllactose (SL) as donor and radioactive lactose as acceptor substrate are widely used to measure TcTS activity. The radioactive sialylated product is then isolated by anion exchange chromatography and measured. Here we describe a new nonradioactive assay using SL or fetuin as donor and benzyl β-D-Fuc-(1→6)-α-D-GlcNAc (1) as acceptor. Disaccharide 1 was easily synthesized by regioselective glycosylation of benzyl α-D-GlcNAc with tetra-Obenzoyl-D-fucose followed by debenzoylation. Compound 1 lacks the hydroxyl group at C-6 of the acceptor galactose and therefore is not a substrate for galactose oxidase. Our method relies on the specific quantification of terminal galactose produced by trans-sialylation from the donor to the 6-deoxy-galactose (D-Fuc) unit of 1 by a spectrophotometric galactose oxidase assay. This method may also discriminate sialidase and trans-sialylation activities by running the assay in the absence of acceptor 1. © The Author 2010. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org. Fil:Agusti, R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Leguizamón, M.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Campetella, O. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:de Lederkremer, R.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
- Subjects :
- anion exchange chromatography
Trans-sialidase
glycosylation
Trypanosoma cruzi
fetuin
Neuraminidase
Oligosaccharides
Structure-Activity Relationship
carbohydrate analysis
spectrophotometry
sialidase inhibitor
Enzyme Inhibitors
enzyme inhibition
enzyme substrate
Glycoproteins
nonhuman
Staining and Labeling
Inhibitors
sialidase
article
Galactose
priority journal
sialic acid
Tetra
Galactose oxidase
Mammalia
Sialic Acids
alpha-Fetoproteins
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Glycobiology 2010;20(8):982-990, Biblioteca Digital (UBA-FCEN), Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales, instacron:UBA-FCEN
- Accession number :
- edsair.od......3056..136799f6a86165605f2da0fdd972d455