1pzk

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Cholera Toxin B-Pentamer Complexed With N-Acyl Phenyl Galactoside 9h

Overview

With the aim of developing high-affinity mono and multivalent antagonists, of cholera toxin (CT) and Escherichia coli heat-labile enterotoxin (LT) we, are using the galactose portion of the natural receptor ganglioside GM1 as, an anchoring fragment in structure-based inhibitor design efforts. In, order to establish a better structure-activity relationship for guiding, these studies, we designed and prepared a small focused library of twenty, 3,5-substituted phenylgalactosides based on two previous leads. The, compounds were tested for their ability to block CTB(5) binding to, immobilized ganglioside receptor and compared to the two previous leads., The crystal structures of the most promising compounds bound to either, CTB(5) or LTB(5) were then determined in order to understand the basis for, affinity differences. The most potent new compound yielded a six-fold, improvement over our benchmark lead, m-nitrophenyl-alpha-d-galactopyranoside (MNPG), and a two-fold improvement, in IC(50) over a newer MNPG derivative. These results support the notion, that the m-nitrophenyl moiety of MNPG and its derivatives is an important, element to retain in future optimization efforts. Additionally, a, consensus binding-pocket for the alkylmorpholine or piperazine moiety, present in all of the designed antagonists was established as an important, area of the GM1 binding site to target in future work.

About this Structure

1PZK is a Single protein structure of sequence from Vibrio cholerae with J12 as ligand. Full crystallographic information is available from OCA.

Reference

3,5-Substituted phenyl galactosides as leads in designing effective cholera toxin antagonists; synthesis and crystallographic studies., Mitchell DD, Pickens JC, Korotkov K, Fan E, Hol WG, Bioorg Med Chem. 2004 Mar 1;12(5):907-20. PMID:14980603

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