In Isothermal Titration Calorimetry (ITC) heat changes associated with chemical reactions are monitored. It is a powerful, label-free, direct method to observe the thermodynamics of binding reactions and to directly characterize enzyme kinetics.

The binding constant (Ka), the stoichiometry (n),ÌýΔH, Δ³Ò,Ìý²¹²Ô»åÌýΔ³§Ìýcan be determined from a single binding experiment. Δ³¦±èÌýcan be determined from the temperature dependency of ΔH observed in multiple experiments at different temperatures.ÌýITC of enzyme-substrate reactions can be used to determine KMÌýand kcat.

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Exciting Possibilities in Biology, Biochemistry and Biophysics


  • Ka, ΔH,ÌýΔ³Ò,ÌýΔ³§,ÌýΔ³¦±è (protein-protein, protein-ligand, DNA/RNA-ligand, DNA/RNA-protein, protein-lipids, peptide-lipids...)
  • ÌýMeasure heat Ìýdirectly
  • Avoid coupled enzyme assay or standard curves
  • Avoid labelingÌýorÌýimmobilizationÌý
  • Use turbid or colored solutions
  • Determine multiple binding affinities and stoichiometries in one system
  • EnzymeÌýkinetics, KM, kcat (in some cases)
  • Inhibitor studies,ÌýKI
  • FoldingÌýreactions (proteins, RNA, DNA)
  • And a lot more...Ìý