Charis Georgiou, Iain McNae, Martin Wear, Harris Ioannidis, Julien Michel, Malcolm Walkinshaw
Journal of molecular biology 2017 Aug 04Fragment-based drug discovery is an increasingly popular method to identify novel small-molecule drug candidates. One of the limitations of the approach is the difficulty of accurately characterizing weak binding events. This work reports a combination of X-ray diffraction, surface plasmon resonance experiments and molecular dynamics simulations for the characterization of binders to different isoforms of the cyclophilin (Cyp) protein family. Although several Cyp inhibitors have been reported in the literature, it has proven challenging to achieve high binding selectivity for different isoforms of this protein family. The present studies have led to the identification of several structurally novel fragments that bind to diverse Cyp isoforms in distinct pockets with low millimolar dissociation constants. A detailed comparison of the merits and drawbacks of the experimental and computational techniques is presented, and emerging strategies for designing ligands with enhanced isoform specificity are described. Copyright © 2017 Elsevier Ltd. All rights reserved.
Charis Georgiou, Iain McNae, Martin Wear, Harris Ioannidis, Julien Michel, Malcolm Walkinshaw. Pushing the Limits of Detection of Weak Binding Using Fragment-Based Drug Discovery: Identification of New Cyclophilin Binders. Journal of molecular biology. 2017 Aug 04;429(16):2556-2570
PMID: 28673552
View Full Text