Towards new glycosyltransferase ligands

  1. Mattia Ghirardello
  2. J. Ignacio Delso
  3. Tomás Tejero
  4. Sonsoles Martin-Santamaria
  5. Ramón Hurtado‐Guerrero
  6. Pedro Merino
Actas:
XII Simposio de Investigadores Jóvenes RSEQ-Sigma Aldrich

Año de publicación: 2015

Congreso: XII Simposio de Investigadores Jóvenes RSEQ Sigma-Aldrich (12º. 2015. Barcelona)

Tipo: Aportación congreso

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Resumen

GalNAc‐T2 is an enzyme that catalyze the transfer of N-Acetylgalactosamine from the donor substrate UDP‐GalNAc to the acceptor hydroxyl groups in mucine-‐type proteins. It belongs to a wide family of glycosyltransferase of which twenty isoforms are present in the human body. At the present time, despite the importance of this enzyme, involved in several metabolic disorders; very few binding substrates exists for this family of enzymes and no inhibitors have been reported. Here, we propose a new method to generate a new family of α-C‐glycoside ligands, based on the reactivity of the phosphonate group, miming the natural substrate but suppressing one phosphate function; leading to a new class of non‐too polar and non-hydrolyzable compounds. We standardize the synthesis on a wide pool of different carbohydrates. Afterwards a docking study confirmed the binding capability of these new molecules with the GalNAc-T2 enzyme and a biological assay and a crystal structure validated the in-silico predicted binding capability. This method can be efficiently used to synthetize a wide variety of new compounds, and is easily extendable to different class of molecules and nucleosides to find new glycosyltransferase ligands.