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Updated: Jul 11, 2026

Collecting Variable-concentration Isothermal Titration Calorimetry Datasets in Order to Determine Binding Mechanisms
Published on: April 7, 2011
Characterization of FOXO3-14-3-3 Interaction by Isothermal Titration Calorimetry
Thazhe Kootteri Prasad1, Sneha Bairy1, Neelagandan Kamariah2
1Centre for Chemical Biology and Therapeutics, Institute for Stem Cell Science and Regenerative Medicine and National Centre for Biological Sciences-TIFR, Bangalore, India.
Abstract:
Isothermal titration calorimetry (ITC) is a well-established and convenient label-free technique for measuring biomolecular interactions in aqueous solutions. ITC enables accurate measurement of the affinities and thermodynamic parameters, such as changes in Gibbs energy, enthalpy, and entropy, which help dissect the binding mechanisms. ITC is commonly used to study protein-protein, protein-peptide, protein-DNA, and small-molecule inhibitor binding to target proteins. ITC can determine binding affinities ranging from nM to low-mM. This chapter provides a detailed protocol to investigate the binding of FOXO3 peptide to 14-3-3ε using ITC.
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