Orthogonal Screening Platforms to Confirm Hits
Charles River offers a range of orthogonal platforms for primary screening, fragment screening, hit confirmation and characterization, hit-to-lead, and lead optimization.
| Surface Plasmon Resonance (SPR): | - A fully equipped suite offering a range of Biacore platforms, complemented with Bruker instrumentation
- Enabled for low, medium, and high throughput analyses
- Binding confirmation, kinetic profiling, MOA investigations (including competition studies), and in-house fragment screening
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| Biochemical Assays: | - Many readouts accommodating high-concentration fragment screening
- Multi-modal fluorescence and luminescence readouts
- Binding assays and many other formats
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| Cellular Assays: | |
| X-Ray Crystallographic Screening: | - Integrated Structural Biology and Protein Science department allows for crystallization using fresh protein
- Weekly slots at both UK and European synchrotron facilities for high-resolution data acquisition
- Access to XCHEM fragment screening at the Diamond Synchrotron, Didcot, UK
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| Nuclear Magnetic Resonance (NMR): | - Access to 600 MHz, five-channel Bruker Avance III spectrometer with a 24-place sample changer and a cryoprobe which can observe a wide range of biologically relevant nuclei at high sensitivity
- Fragment screening using in-house fluorinated fragment library
- Ligand observed binding through STD, CPMG, and WaterLOGSY experiments
- Protein observed ligand binding, backbone assignments, and mapping of ligand binding site
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| SAMDI-MS: | - Combination of surface chemistry and MALDI TOF MS
- Premier label-free and high-throughput assay
- Analysis of biochemical (functional) activities and affinity selection MS to discover small molecule binders to protein and oligonucleotide (RNA targets)
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