4.4 Article

Design of Triazole-Tethered Glycoclusters Exhibiting Three Different Spatial Arrangements and Comparative Study of their Affinities towards PA-IL and RCA 120 by Using a DNA-Based Glycoarray

Journal

CHEMBIOCHEM
Volume 10, Issue 8, Pages 1369-1378

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.200900024

Keywords

calixarenes; click chemistry; glycoarrays; glycoclusters; multivalency

Funding

  1. CNRS
  2. ANR [ANR-08-BLAN-0114-01]
  3. Lyon Biopole
  4. Agence Nationale de la Recherche (ANR) [ANR-08-BLAN-0114] Funding Source: Agence Nationale de la Recherche (ANR)

Ask authors/readers for more resources

Interactions between proteins and carbohydrates are involved in a large number of crucial biological events. Many efforts have been devoted to the design and synthesis of unnatural saccharides displaying high affinities towards targeted lectins. Among others, glycoside clusters have proven to be valuable tools for these recognition studies. However, the spatial arrangements of the sugar residues are a key issue in the design of high-affinity glycoclusters. Here, the affinities of linear and antenna- and calixarene-based galactoside clusters against two lectins, derived from Pseudomonas aeruginosa and Ricinus communis, have been compared by means of glycoarrays.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available