Literature DB >> 34395765

Isothermal Titration Calorimetry: A Biophysical Method to Characterize the Interaction between Label-free Biomolecules in Solution.

Andrea Saponaro1.   

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.
Copyright © 2018 The Authors; exclusive licensee Bio-protocol LLC.

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


  2 in total

1.  Rapid measurement of binding constants and heats of binding using a new titration calorimeter.

Authors:  T Wiseman; S Williston; J F Brandts; L N Lin
Journal:  Anal Biochem       Date:  1989-05-15       Impact factor: 3.365

2.  Fusicoccin Activates KAT1 Channels by Stabilizing Their Interaction with 14-3-3 Proteins.

Authors:  Andrea Saponaro; Alessandro Porro; Antonio Chaves-Sanjuan; Marco Nardini; Oliver Rauh; Gerhard Thiel; Anna Moroni
Journal:  Plant Cell       Date:  2017-09-29       Impact factor: 11.277

  2 in total
  1 in total

Review 1.  Biophysical Approaches for the Characterization of Protein-Metabolite Interactions.

Authors:  Anja Thalhammer; Nina K Bröker
Journal:  Methods Mol Biol       Date:  2023
  1 in total

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