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J Med Chem. 2012 Feb 9;55(3):1287-95. doi: 10.1021/jm201439b. Epub 2012 Jan 24.

Binding evaluation of fragment-based scaffolds for probing allosteric enzymes.

Author information

1
Institut des Sciences Analytiques, UMR CNRS 5280, Université de Lyon, Université Claude Bernard Lyon 1, Bât. CPE Lyon, Domaine scientifique de la Doua, F-69622 Villeurbanne, France. isabelle.krimm@univ-lyon1.fr

Abstract

Fragment-based drug discovery has become a powerful method for the generation of drug leads against therapeutic targets. Beyond the identification of novel and effective starting points for drug design, fragments have emerged as reliable tools for assessing protein druggability and identifying protein hot spots. Here, we have examined fragments resulting from the deconstruction of known inhibitors from the glycogen phosphorylase enzyme, a therapeutic target against type 2 diabetes, with two motivations. First, we have analyzed the fragment binding to the multiple binding sites of the glycogen phosphorylase, and then we have investigated the use of fragments to study allosteric enzymes. The work we report illustrates the power of fragmentlike ligands not only for probing the various binding pockets of proteins, but also for uncovering cooperativity between these various binding sites.

PMID:
22229710
DOI:
10.1021/jm201439b
[Indexed for MEDLINE]

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