| Autor: |
Gee CT; Department of Chemistry, University of Minnesota, Minneapolis, Minnesota, USA., Arntson KE; Department of Chemistry, University of Minnesota, Minneapolis, Minnesota, USA., Urick AK; Department of Chemistry, University of Minnesota, Minneapolis, Minnesota, USA., Mishra NK; Department of Chemistry, University of Minnesota, Minneapolis, Minnesota, USA., Hawk LM; Department of Chemistry, University of Minnesota, Minneapolis, Minnesota, USA., Wisniewski AJ; Department of Medicinal Chemistry, University of Minnesota, Minneapolis, Minnesota, USA., Pomerantz WC; Department of Chemistry, University of Minnesota, Minneapolis, Minnesota, USA. |
| Abstrakt: |
NMR spectroscopy can be used to quantify the binding affinity between proteins and low-complexity molecules, termed 'fragments'; this versatile screening approach allows researchers to assess the druggability of new protein targets. Protein-observed (19)F-NMR (PrOF NMR) using (19)F-labeled amino acids generates relatively simple spectra that are able to provide dynamic structural information toward understanding protein folding and function. Changes in these spectra upon the addition of fragment molecules can be observed and quantified. This protocol describes the sequence-selective labeling of three proteins (the first bromodomains of Brd4 and BrdT, and the KIX domain of the CREB-binding protein) using commercially available fluorinated aromatic amino acids and fluorinated precursors as example applications of the method developed by our research group. Fragment-screening approaches are discussed, as well as Kd determination, ligand-efficiency calculations and druggability assessment, i.e., the ability to target these proteins using small-molecule ligands. Experiment times on the order of a few minutes and the simplicity of the NMR spectra obtained make this approach well-suited to the investigation of small- to medium-sized proteins, as well as the screening of multiple proteins in the same experiment. |
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