Pulse dipolar EPR for determining nanomolar binding affinities
Katrin Ackermann, Joshua L. Wort, Bela E. Bode
Abstract
Protein interaction studies often require very low concentrations and highly sensitive biophysical methods. Here, we demonstrate that pulse dipolar electron paramagnetic resonance spectroscopy allows measuring dissociation constants in the nanomolar range. This approach is appealing for concentration-limited biomolecular systems and medium-to-high-affinity binding studies, demonstrated here at 50 nanomolar protein concentration.
Topics & Concepts
Electron paramagnetic resonanceDissociation constantAffinitiesChemistryElectron paramagnetic resonance spectroscopyBinding affinitiesPulsed EPRDissociation (chemistry)DipoleMolecular bindingBiophysicsNuclear magnetic resonanceAnalytical Chemistry (journal)MoleculePhysical chemistryStereochemistryBiochemistryMagnetic resonance imagingChromatographySpin echoOrganic chemistryBiologyMedicineRadiologyReceptorPhysicsElectron Spin Resonance StudiesElectrochemical Analysis and ApplicationsSpectroscopy and Quantum Chemical Studies