Rapid Protein-Ligand Affinity Determination by Photoinduced Hyperpolarized NMR.
Ontology highlight
ABSTRACT: The binding affinity determination of protein-ligand complexes is a cornerstone of drug design. State-of-the-art techniques are limited by lengthy and expensive processes. Building upon our recently introduced novel screening method utilizing photochemically induced dynamic nuclear polarization (photo-CIDNP) NMR, we provide the methodological framework to determine binding affinities within 5-15 min using 0.1 mg of protein. The accuracy of our method is demonstrated for the affinity constants of peptides binding to a PDZ domain and fragment ligands binding to the protein PIN1. The method can also be extended to measure the affinity of nonphoto-CIDNP-polarizable ligands in competition binding experiments. Finally, we demonstrate a strong correlation between the ligand-reduced signals in pho
SUBMITTER: Butikofer M
PROVIDER: S-EPMC11228983 | biostudies-literature | 2024 Jul
REPOSITORIES: biostudies-literature
ACCESS DATA