Abstract:
The synthesis of mono and divalent β-galactosylamides linked to a hydroxylated chain having a C2 symmetry axis derived from L-tartaric anhydride is reported. Reference compounds devoid of hydroxyl groups in the linker were also prepared from β-galactosylamine and succinic anhydride. After functionalization with an alkynyl residue, the resulting building blocks were grafted onto different azide-equipped scaffolds through the copper catalyzed azide-alkyne cycloaddition. Thus, a family of structurally related mono and divalent β-N-galactopyranosylamides was obtained and fully characterized. The binding affinities of the ligands towards the model lectin PNA were measured by the enzyme-linked lectin assay (ELLA). The IC50 values were significantly higher than that of galactose but the presence of hydroxyl groups in the aglycone chain improved lectin recognition. Docking and molecular dynamics experiments were in accordance with the hypothesis that a hydroxyl group properly disposed in the linker could mimic the Glc O3 in the recognition process. On the other hand, divalent presentation of the ligands led to lectin affinity enhancements. © 2017 Elsevier Ltd
Registro:
Documento: |
Artículo
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Título: | Synthesis of β-galactosylamides as ligands of the peanut lectin. Insights into the recognition process |
Autor: | Cano, M.E.; Varela, O.; García-Moreno, M.I.; García Fernández, J.M.; Kovensky, J.; Uhrig, M.L. |
Filiación: | Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Química Orgánica, Ciudad Universitaria, Pabellón 2, Buenos Aires, C1428EHA, Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)-UBA, Centro de Investigación en Hidratos de Carbono (CIHIDECAR), Buenos Aires, Argentina Departamento de Química Orgánica, Facultad de Química, Universidad de Sevilla, c/ Profesor García González 1, Sevilla, 41012, Spain Instituto de Investigaciones Químicas (IIQ), CSIC - Universidad de Sevilla, Avda. Américo Vespucio 49, Sevilla, 41092, Spain Laboratoire de Glycochimie, des Antimicrobiens et des Agroressources (LG2A)-CNRS UMR 7378, Université de Picardie Jules Verne, 33 rue Saint Leu, Amiens Cedex, 80039, France
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Palabras clave: | Divalent ligands; ELLA assay; Molecular dynamics; Peanut agglutinin; β-galactosylamides; Binding energy; Chains; Chelation; Ligands; Molecular dynamics; Oilseeds; Proteins; Scaffolds; Azide-alkyne cycloaddition; Binding affinities; Functionalizations; Lectin recognition; Peanut agglutinin; Recognition process; Reference compounds; Succinic anhydride; Copper compounds; aglycone; alkyne; amide; azide; beta galactosylamide; copper; hydroxyl group; lectin; ligand; succinic anhydride; unclassified drug; galactose; ligand; peanut agglutinin; protein binding; Article; catalysis; controlled study; cycloaddition; enzymatic assay; hydroxylation; IC50; molecular docking; molecular dynamics; molecular recognition; peanut; priority journal; synthesis; chemistry; metabolism; molecular model; protein conformation; Galactose; Ligands; Models, Molecular; Peanut Agglutinin; Protein Binding; Protein Conformation |
Año: | 2017
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Volumen: | 443-444
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Página de inicio: | 58
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Página de fin: | 67
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DOI: |
http://dx.doi.org/10.1016/j.carres.2017.03.018 |
Título revista: | Carbohydrate Research
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Título revista abreviado: | Carbohydr. Res.
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ISSN: | 00086215
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CODEN: | CRBRA
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CAS: | amide, 17655-31-1; azide, 12596-60-0, 14343-69-2; copper, 15158-11-9, 7440-50-8; succinic anhydride, 108-30-5; galactose, 26566-61-0, 50855-33-9, 59-23-4; Galactose; Ligands; Peanut Agglutinin
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Registro: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v443-444_n_p58_Cano |
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Citas:
---------- APA ----------
Cano, M.E., Varela, O., García-Moreno, M.I., García Fernández, J.M., Kovensky, J. & Uhrig, M.L.
(2017)
. Synthesis of β-galactosylamides as ligands of the peanut lectin. Insights into the recognition process. Carbohydrate Research, 443-444, 58-67.
http://dx.doi.org/10.1016/j.carres.2017.03.018---------- CHICAGO ----------
Cano, M.E., Varela, O., García-Moreno, M.I., García Fernández, J.M., Kovensky, J., Uhrig, M.L.
"Synthesis of β-galactosylamides as ligands of the peanut lectin. Insights into the recognition process"
. Carbohydrate Research 443-444
(2017) : 58-67.
http://dx.doi.org/10.1016/j.carres.2017.03.018---------- MLA ----------
Cano, M.E., Varela, O., García-Moreno, M.I., García Fernández, J.M., Kovensky, J., Uhrig, M.L.
"Synthesis of β-galactosylamides as ligands of the peanut lectin. Insights into the recognition process"
. Carbohydrate Research, vol. 443-444, 2017, pp. 58-67.
http://dx.doi.org/10.1016/j.carres.2017.03.018---------- VANCOUVER ----------
Cano, M.E., Varela, O., García-Moreno, M.I., García Fernández, J.M., Kovensky, J., Uhrig, M.L. Synthesis of β-galactosylamides as ligands of the peanut lectin. Insights into the recognition process. Carbohydr. Res. 2017;443-444:58-67.
http://dx.doi.org/10.1016/j.carres.2017.03.018