High-Throughput Binding Kinetic Measurements of DNA-Encoded Library-Derived Hits By Focal Molography
DNA-encoded libraries (DELs) enable rapid discovery of large pools of small organic ligands against target proteins. Currently available hit validation methodologies are limited in their ability to characterize binding kinetics for a large number of molecules. Only a subset of hits identified by DEL screening are followed up on, while many potentially relevant binders remain uncharacterized. Here, we propose focal molography as a high-throughput, label-free optical methodology for parallel kinetic measurements of DEL-derived hits. The methodology was applied to measure binding kinetics ( k on and k off ) and dissociation constants ( K d ) of DEL-derived ligands against carbonic anhydrase IX and of known ligands to fibroblast activation protein. The binding parameters obtained were consistent with fluorescence polarization, surface plasmon resonance, and inhibition measurements. The data reported in this manuscript support the use of focal molography as a robust DEL-compatible technology for quantitative, high-throughput hit validation.
Authors
- Sara Puglioli (ORCID: https://orcid.org/0000-0002-4795-7331)
- Nicholas Favalli (ORCID: https://orcid.org/0000-0002-6538-7379)
- Andreas Frutiger (ORCID: https://orcid.org/0000-0002-2523-8918)
- Samuele Cazzamalli (ORCID: https://orcid.org/0000-0003-0510-5664)
- Lukas Heuberger (ORCID: https://orcid.org/0000-0003-4110-9742)
- D Neri
- Sebastian Oehler (ORCID: https://orcid.org/0000-0003-2013-7381)
- Marco Müller (ORCID: https://orcid.org/0009-0009-7277-1246)
- Mosè Fabbri
- Carola Velti
- Lorenzo Campari
Institutions
- Linde (United States) (US)
- Philogen (Italy) (IT)
- Philochem (Switzerland) (CH)
- École Polytechnique Fédérale de Lausanne (CH)
Publication Details
- Journal
- Journal of Medicinal Chemistry
- Published
- 2026-06-16
- DOI
- https://doi.org/10.1021/acs.jmedchem.6c01097
- Primary Topic
- Click Chemistry and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00