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Accurate protein-peptide titration experiments by nuclear magnetic resonance using low-volume samples

Abstract : NMR spectroscopy allows measurements of very accurate values of equilibrium dissociation constants using chemical shift perturbation methods, provided that the concentrations of the binding partners are known with high precision and accuracy. The accuracy and precision of these experiments are improved if performed using individual capillary tubes, a method enabling full automation of the measurement. We provide here a protocol to set up and perform these experiments as well as a robust method to measure peptide concentrations using tryptophan as an internal standard.
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Christian Kohler, Raphaël Recht, Marc Quinternet, Frédéric de Lamotte, Marc-André Delsuc, et al.. Accurate protein-peptide titration experiments by nuclear magnetic resonance using low-volume samples. Affinity Chromatography : Methods and Protocols, 1286, Humana Press, 341 p., 2015, Methods in Molecular Biology, 978-1-4939-2447-9. ⟨10.1007/978-1-4939-2447-9_22⟩. ⟨hal-02801062⟩

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