| Literature DB >> 34395765 |
Abstract
This protocol can be applied to analyze the direct interaction between a soluble protein and a target ligand molecule using Isothermal Titration Calorimetry (ITC, Malvern). ITC allows the biophysical characterization of binding between label-free, non-immobilized and in-solution biomolecules by providing the stoichiometry of the interaction, the equilibrium binding constants and the thermodynamic parameters. ITC monitors heat changes (released and/or absorbed) caused by macromolecular interactions with no restrictions of buffer and molecular weight of the macromolecules.Entities:
Keywords: 14-3-3 proteins; Binding affinity; Calorimetry; ITC; KAT1 channels; Macromolecular interaction
Year: 2018 PMID: 34395765 PMCID: PMC8328675 DOI: 10.21769/BioProtoc.2957
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325