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Fucosylated pentaerythrityl phosphodiester oligomers (PePOs): automated synthesis of DNA-based glycoclusters and binding to Pseudomonas aeruginosa lectin (PA-IIL)
Authors:Morvan François  Meyer Albert  Jochum Anne  Sabin Charles  Chevolot Yann  Imberty Anne  Praly Jean-Pierre  Vasseur Jean-Jacques  Souteyrand Eliane  Vidal Sébastien
Affiliation:Institut des Biomolécules Max Mousseron, UMR 5247 CNRS - Université Montpellier I - Université Montpellier II, LACAN, CC008, Place E. Bataillon, 34095 Montpellier Cedex 5, France.
Abstract:
The synthesis of propargylated pentaerythrityl phosphodiester oligomers (PePOs) was achieved using a DNA synthesizer with a bis-propargylated pentaerythritol-based phosphoramidite. An azido fucose derivative was reacted under "click" chemistry conditions activated by microwaves to construct a series of glycosylated PePOs bearing 4, 6, 8, and 10 L-fucose residues. Binding to the fucose-specific bacterial lectin (PA-IIL) was determined for the fucosylated PePOs through an enzyme-linked lectin amplification competition assay. The IC50 values measured are 10-20 times better than for monovalent l-fucose and denotate for a "macromolecular" effect rather than a "cluster" effect.
Keywords:
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