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Uptake and release protocol for assessing membrane binding and permeation by way of isothermal titration calorimetry

Abstract

The activity of many biomolecules and drugs crucially depends on whether they bind to biological membranes and whether they translocate to the opposite lipid leaflet and trans aqueous compartment. A general strategy to measure membrane binding and permeation is the uptake and release assay, which compares two apparent equilibrium situations established either by the addition or by the extraction of the solute of interest. Only solutes that permeate the membrane sufficiently fast do not show any dependence on the history of sample preparation. This strategy can be pursued for virtually all membrane-binding solutes, using any method suitable for detecting binding. Here, we present in detail one example that is particularly well developed, namely the nonspecific membrane partitioning and flip-flop of small, nonionic solutes as characterized by isothermal titration calorimetry. A complete set of experiments, including all sample preparation procedures, can typically be accomplished within 2 days. Analogous protocols for studying charged solutes, virtually water-insoluble, hydrophobic compounds or specific ligands are also considered.

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Figure 1: Schematic illustration of uptake and release experiments.
Figure 2: Uptake and release experiments with SDS at 25 °C (a,b) and 65 °C (c,d).

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References

  1. Seelig, J. & Ganz, P. Nonclassical hydrophobic effect in membrane binding equilibria. Biochemistry 30, 9354–9359 (1991).

    Article  CAS  Google Scholar 

  2. Seelig, J. Titration calorimetry of lipid–peptide interactions. Biochim. Biophys. Acta 1331, 103–116 (1997).

    Article  CAS  Google Scholar 

  3. Heerklotz, H. & Seelig, J. Titration calorimetry of surfactant-membrane partitioning and membrane solubilization. Biochim. Biophys. Acta 1508, 69–85 (2000).

    Article  CAS  Google Scholar 

  4. Lin, L.N., Li, J.Y., Brandts, J.F. & Weiss, R.M. The serine receptor of bacterial chemotaxis exhibits half-site saturation for serine binding. Biochemistry 33, 6564–6570 (1994).

    Article  CAS  Google Scholar 

  5. Heerklotz, H., Lantzsch, G., Binder, H., Klose, G. & Blume, A. Thermodynamic characterization of dilute aqueous lipid/detergent mixtures of POPC and C12EO8 by means of isothermal titration calorimetry. J. Phys. Chem. 100, 6764–6774 (1996).

    Article  CAS  Google Scholar 

  6. Ladbury, J.E. Application of isothermal titration calorimetry in the biological sciences: things are heating up!. Biotechniques 37, 885–887 (2004).

    Article  CAS  Google Scholar 

  7. Ladbury, J. E. & Doyle, M. L. (eds.) Biocalorimetry Vol. 2 (Wiley-VCH, Weinheim, Germany, 2004).

    Book  Google Scholar 

  8. Heerklotz, H. Microcalorimetry of lipid membranes. J. Phys.: Condens. Matter 16, R441–R467 (2004).

    CAS  Google Scholar 

  9. Heerklotz, H.H., Binder, H. & Epand, R.M. A “release” protocol for isothermal titration calorimetry. Biophys. J. 76, 2606–2613 (1999).

    Article  CAS  Google Scholar 

  10. Heerklotz, H., Szadkowska, H., Anderson, T. & Seelig, J. The sensitivity of lipid domains to small perturbations demonstrated by the effect of triton. J. Mol. Biol. 329, 793–799 (2003).

    Article  CAS  Google Scholar 

  11. Tsamaloukas, A., Szadkowska, H. & Heerklotz, H. Nonideal mixing in multicomponent lipid/detergent systems. J. Phys.: Condens. Matter 18 (2006).

  12. Hagen, V. et al. Coumarinylmethyl esters for ultrafast release of high concentrations of cyclic nucleotides upon one- and two-photon photolysis. Angew. Chem. Int. Ed. Engl. 44, 7887–7891 (2005).

    Article  CAS  Google Scholar 

  13. Heerklotz, H. Membrane stress and permeabilization induced by asymmetric incorporation of compounds. Biophys. J. 81, 184–195 (2001).

    Article  CAS  Google Scholar 

  14. Keller, S., Heerklotz, H. & Blume, A. Monitoring lipid membrane translocation of sodium dodecyl sulfate by isothermal titration calorimetry. J. Am. Chem. Soc. 128, 1279–1286 (2006).

    Article  CAS  Google Scholar 

  15. Montich, G., Scarlata, S., McLaughlin, S., Lehrmann, R. & Seelig, J. Thermodynamic characterization of the association of small basic peptides with membranes containing acidic lipids. Biochim. Biophys. Acta 1146, 17–24 (1993).

    Article  CAS  Google Scholar 

  16. Murray, D. et al. Electrostatic properties of membranes containing acidic lipids and adsorbed basic peptides: theory and experiment. Biophys. J. 77, 3176–3188 (1999).

    Article  CAS  Google Scholar 

  17. Cambridge, S.B., Geissler, D., Keller, S. & Curten, B. A caged doxycycline analogue for photoactivated gene expression. Angew. Chem. Int. Ed. Engl. 45, 2229–2231 (2006).

    Article  CAS  Google Scholar 

  18. Gilbert, D. et al. Caged Capsaicins: new tools for the examination of TRPV1 channels in somatosensory neurons. ChemBioChem 8, 89–97 (2007).

    Article  CAS  Google Scholar 

  19. Bárány-Wallje, E. et al. A critical reassessment of penetratin translocation across lipid membranes. Biophys. J. 89, 2513–2521 (2005).

    Article  Google Scholar 

  20. Keller, S., Böthe, M., Bienert, M., Dathe, M. & Blume, A. A simple fluorescence-spectroscopic membrane translocation assay. ChemBioChem DOI: 10.1002/cbic.200600553.

    Article  CAS  Google Scholar 

  21. Tsamaloukas, A., Szadkowska, H., Slotte, P.J. & Heerklotz, H. Interactions of cholesterol with lipid membranes and cyclodextrin characterized by calorimetry. Biophys. J. 89, 1109–1119 (2005).

    Article  CAS  Google Scholar 

  22. Murphy, K.P. Predicting binding energetics from structure: looking beyond ΔG0 . Med. Res. Rev. 19, 333–339 (1999).

    Article  CAS  Google Scholar 

  23. Spolar, R.S., Ha, J.H. & Record, M.T. Jr. Hydrophobic effect in protein folding and other noncovalent processes involving proteins. Proc. Natl. Acad. Sci. USA 86, 8382–8385 (1989).

    Article  CAS  Google Scholar 

  24. Kresheck, G.C. & Hargraves, W.A. Thermometric titration studies of the effect of head group, chain length, solvent, and temperature on the thermodynamics of micelle formation. J. Coll. Interf. Sci. 48, 481–493 (1974).

    Article  CAS  Google Scholar 

  25. Hope, M.J., Bally, M.B., Webb, G. & Cullis, P.R. Production of large unilamellar vesicles by a rapid extrusion procedure. Characterization of size distribution, trapped volume and ability to maintain a membrane potential. Biochim. Biophys. Acta 812, 55–65 (1985).

    Article  CAS  Google Scholar 

  26. Record, M.T. Jr., Lohman, T.M. & De Haseth, P. Ion effects on ligand nucleic acid interactions. J. Mol. Biol. 107, 145–158 (1976).

    Article  CAS  Google Scholar 

  27. Mascotti, D.P. & Lohman, T.M. Thermodynamic extent of counterion release upon binding oligolysines to single-stranded nucleic acids. Proc. Natl. Acad. Sci. USA 87, 3142–3146 (1990).

    Article  CAS  Google Scholar 

  28. Patel, D.R. et al. Calcium-dependent binding of annexin 12 to phospholipid bilayers: stoichiometry and implications. Biochemistry 40, 7054–7060 (2001).

    Article  CAS  Google Scholar 

  29. Chellani, M. Isothermal titration calorimetry: biological applications. Am. Biotechnol. Lab. 17, 14–18 (1999).

    CAS  Google Scholar 

  30. MacDonald, R.C. et al. Small-volume extrusion apparatus for preparation of large, unilamellar vesicles. Biochim. Biophys. Acta 1061, 297–303 (1991).

    Article  CAS  Google Scholar 

  31. Wieprecht, T., Apostolov, O., Beyermann, M. & Seelig, J. Thermodynamics of the alpha-helix–coil transition of amphipathic peptides in a membrane environment: implications for the peptide-membrane binding equilibrium. J. Mol. Biol. 294, 785–794 (1999).

    Article  CAS  Google Scholar 

  32. Tsamaloukas, A., Szadkowska, H. & Heerklotz, H. Thermodynamic comparison of the interactions of cholesterol with unsaturated phospholipid and sphingomyelins. Biophys. J. 90, 4479–4487 (2006).

    Article  CAS  Google Scholar 

  33. Keller, M., Kerth, A. & Blume, A. Thermodynamics of interaction of octyl glucoside with phosphatidylcholine vesicles: partitioning and solubilization as studied by high sensitivity titration calorimetry. Biochim. Biophys. Acta 1326, 178–192 (1997).

    Article  CAS  Google Scholar 

  34. Heerklotz, H., Binder, H., Lantzsch, G., Klose, G. & Blume, A. Lipid/detergent interaction thermodynamics as a function of molecular shape. J. Phys. Chem. B 101, 639–645 (1997).

    Article  CAS  Google Scholar 

  35. Wenk, M.R., Alt, T., Seelig, A. & Seelig, J. Octyl-β-D-glucopyranoside partitioning into lipid bilayers: thermodynamics of binding and structural changes of the bilayer. Biophys. J. 72, 1719–1731 (1997).

    Article  CAS  Google Scholar 

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Acknowledgements

We dedicate this publication to Professor Joachim Seelig of the Biozentrum of the University of Basel, on the occasion of his 65th birthday. He has played a seminal role in the development of membrane microcalorimetry. We are indebted to him for the friendly uptake into his laboratory, his invaluable advice and support and the generous release into the freedom to pursue our own projects and plans. We thank Natalie Bordag for help with compiling the fitting routine. This work was supported by a fellowship within the Postdoc Program of the German Academic Exchange Service (DAAD) to A.D.T., by grant no. QLK3-CT-2002-01989 of the European Commission to S.K. and by grant no. 31-67216.01 of the Swiss National Science foundation to H.H.

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Correspondence to Heiko Heerklotz.

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Uptake & Release for Nonionics, © Tsamaloukas, Keller, and Heerklotz (November 2006) (XLS 256 kb)

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Tsamaloukas, A., Keller, S. & Heerklotz, H. Uptake and release protocol for assessing membrane binding and permeation by way of isothermal titration calorimetry. Nat Protoc 2, 695–704 (2007). https://doi.org/10.1038/nprot.2007.98

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