4.4 Article

Isothermal Titration Calorimetry for Measuring Macromolecule-Ligand Affinity

Journal

JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
Volume -, Issue 55, Pages -

Publisher

JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/2796

Keywords

Molecular Biology; Issue 55; Isothermal titration calorimetry; thermodynamics; binding affinity; enthalpy; entropy; free energy

Funding

  1. NSF grant [MCB-0817827]

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Isothermal titration calorimetry (ITC) is a useful tool for understanding the complete thermodynamic picture of a binding reaction. In biological sciences, macromolecular interactions are essential in understanding the machinery of the cell. Experimental conditions, such as buffer and temperature, can be tailored to the particular binding system being studied. However, careful planning is needed since certain ligand and macromolecule concentration ranges are necessary to obtain useful data. Concentrations of the macromolecule and ligand need to be accurately determined for reliable results. Care also needs to be taken when preparing the samples as impurities can significantly affect the experiment. When ITC experiments, along with controls, are performed properly, useful binding information, such as the stoichiometry, affinity and enthalpy, are obtained. By running additional experiments under different buffer or temperature conditions, more detailed information can be obtained about the system. A protocol for the basic setup of an ITC experiment is given.

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