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Thermodynamic Analysis of Protein–Lipid Interactions by Isothermal Titration Calorimetry

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Lipid-Protein Interactions

Part of the book series: Methods in Molecular Biology ((MIMB,volume 2003))

Abstract

Isothermal titration calorimetry is a highly sensitive and powerful technique for the study of molecular interactions. This method can be applied universally for studying the interaction between moleculeAbstracts, molecular assembles and ions as it measures the heat changes resulting from such interactions and does not need any probe molecule/moiety to be incorporated into the system under investigation. This method has been applied quite extensively to investigate the interaction of proteins with other biomolecules such as small ligands, other proteins, nucleic acids, lipid membranes as well as to study the interaction of antibodies, drugs, metal ions and nanoparticles with target proteins or antigens, nucleic acids, and membranes. In this chapter, we describe the application of ITC for the investigation of thermodynamics of protein–lipid interaction. A number of important parameters such as enthalpy of binding (ΔH), entropy of binding (ΔS), association constant (Ka), binding stoichiometry (n) and free energy of binding (ΔG) can be obtained from a single calorimetric titration, providing a complete thermodynamic characterization of the interaction. The method is described in detail taking the major protein of the bovine seminal plasma, PDC-109, which exhibits a high preference for interaction with choline-containing lipids, as an example. The method can be applied to investigate thermodynamic parameters associated with the interaction of other soluble proteins with lipid membranes.

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Acknowledgments

M.J.S. acknowledges the Department of Science and Technology (India) for a research grant which supported the work done in his laboratory and referred to here. R.S.S. and B.P.S. thank CSIR (India) and UGC (India) for Senior Research Fellowships. We thank Dr. V. Anbazhagan for a fruitful collaboration in the ITC studies on protein–lipid interaction.

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Authors and Affiliations

  1. School of Chemistry, University of Hyderabad, Hyderabad, India

    Musti J. Swamy, Rajeshwer S. Sankhala & Bhanu Pratap Singh

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  1. Musti J. Swamy
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  2. Rajeshwer S. Sankhala
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  3. Bhanu Pratap Singh
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Editors and Affiliations

  1. Department of Biophysics, Institute of Biology, FB10 and Center for Interdisciplinary Nanostructure Science and Technology (CINSaT), University of Kassel, Kassel, Germany

    Jörg H. Kleinschmidt

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Swamy, M.J., Sankhala, R.S., Singh, B.P. (2019). Thermodynamic Analysis of Protein–Lipid Interactions by Isothermal Titration Calorimetry. In: Kleinschmidt, J. (eds) Lipid-Protein Interactions. Methods in Molecular Biology, vol 2003. Humana, New York, NY. https://doi.org/10.1007/978-1-4939-9512-7_4

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  • DOI: https://doi.org/10.1007/978-1-4939-9512-7_4

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  • Publisher Name: Humana, New York, NY

  • Print ISBN: 978-1-4939-9511-0

  • Online ISBN: 978-1-4939-9512-7

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