CIHIDECAR   12529
CENTRO DE INVESTIGACIONES EN HIDRATOS DE CARBONO
Unidad Ejecutora - UE
artículos
Título:
Synthesis and characterization of a-D-Galp-(1→3)-b-D-Galp epitopecontaining neoglycoconjugates for Chagas disease serodiagnosis
Autor/es:
GIORGI, M. EUGENIA; DE LEDERKREMER, ROSA M.; LOPEZ, ROSANA; DUCREY, IVANA; MELGAREJO, LINDA TORO; MARINO, CARLA
Revista:
CARBOHYDRATE RESEARCH
Editorial:
ELSEVIER SCI LTD
Referencias:
Lugar: Amsterdam; Año: 2019
ISSN:
0008-6215
Resumen:
The immunodominant epitope α-D-Galp-(1→3)-β-D-Galp-(1→4)-D-GlcNAc, expressed in the mucins of the infective trypomastigote stage of Trypanosoma cruzi has been proposed for multiple clinical applications, from serodiagnosis of protozoan caused diseases to xenotransplantation or cancer vaccinology. It was previously shown that the analogue trisaccharide, with glucose in the reducing end instead of GlcNAc, was as efficient as the natural trisaccharidefor recognition of chagasic antibodies. Here we describe the synthesis of α-D-Galp-(1→3)-β-D-Galp-(1→4)-D-Glcp functionalized as the 6-aminohexyl glycoside and its conjugation to BSA using the squarate method. The conjugate of 6-aminohexyl α-D-Galp-(1→3)-β-D-Galp was also prepared. Both neoglycoconjugates were recognized by serum samples of Trypanosoma cruzi-infected individuals and thus, are promising tools for the improvement of Chagas disease diagnostic applications.