A False‐Positive Screening Hit in Fragment‐Based Lead Discovery: Watch out for the Red Herring. Issue 7 (18th January 2017)

• Record Type: Journal Article
• Authors: Cramer, Jonathan; Schiebel, Johannes; Wulsdorf, Tobias; Grohe, Kristof; Najbauer, Eszter Eva; Ehrmann, Frederik R.; Radeva, Nedyalka; Zitzer, Nina; Linne, Uwe; Linser, Rasmus; Heine, Andreas; Klebe, Gerhard
• Is Part Of: Angewandte Chemie international edition. Volume 56:Issue 7(2017)
• Page Start: 1908
• Page End: 1913
• Publication Date: 2017-01-18
• Subjects: drug discovery -- fragment-based lead discovery -- medicinal chemistry -- PAINS -- reactivity; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.201609824
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: With the rising popularity of fragment‐based approaches in drug development, more and more attention has to be devoted to the detection of false‐positive screening results. In particular, the small size and low affinity of fragments drives screening techniques to their limit. The pursuit of a false‐positive hit can cause significant loss of time and resources. Here, we present an instructive and intriguing investigation into the origin of misleading assay results for a fragment that emerged as the most potent binder for the aspartic protease endothiapepsin (EP) across multiple screening assays. This molecule shows its biological effect mainly after conversion into another entity through a reaction cascade that involves major rearrangements of its heterocyclic scaffold. The formed ligand binds EP through an induced‐fit mechanism involving remarkable electrostatic interactions. Structural information in the initial screening proved to be crucial for the identification of this false‐positive hit. Abstract : Hit or miss ? In fragment‐based drug design, false‐positive screening hits can easily set a research effort on the wrong track. In this study, the intrinsic reactivity of a fragment was identified as the origin of misleading results from previous affinity studies with the protease endothiapepsin. The chemical structure of the fragment derivative identified from the crystal structure and a mechanism for its formation are presented.