The critical micellar concentration (cmc) and the demicellization enthalpy ΔH demic of the primary aggregates of sodium cholate (NaC) and sodium deoxycholate (NaDC) in water and 0.1 M NaCl at pH 7.5 were determined by isothermal titration calorimetry (ITC). The cmc of NaC and NaDC in water and 0.1 M NaCl at pH 7.5 shows a minimum between 295 and 300 K. With increasing ionic strength, the cmc of the bile salts decreases. ΔH demic is strongly temperature-dependent but shows almost no dependence on the ionic strength. For comparison with other systems, the thermodynamic parameters ΔG demic and ΔS demic associated with the demicellization process were calculated using the pseudo-phase-separation model. From the temperature dependence of ΔH demic, the change in heat capacity ΔCp demic for the demicellization process was determined. The data obtained for ΔCp demic are positive and at 298 K have values of 250 J·mol-1·K-1 for NaC and 350 J·mol-1·K-1 for NaDC. These values correspond to changes in the exposed hydrophobic surface area of 1.1−1.5 nm2 per molecule. For NaDC, ΔCp demic decreases at 343 K to ∼250 J·mol-1·K-1, whereas ΔCp demic for NaC remains essentially unchanged. The calorimetric titration curves were simulated using a mass action model including counterion condensation for the aggregation process. The simulation of the titration curves yielded values for the aggregation number n. In the concentration region of the cmc, n is approximately 4−6 for NaC in water or 0.1 M NaCl and independent of temperature. For NaDC in water values of n of 7 and 12 were obtained at low temperature (284 K) in water and 0.1 M NaCl, respectively. For NaDC in water and 0.1 M NaCl, the aggregation number n decreases to 5 and 7, respectively, at 328 K.

Isothermal titration calorimetry (ITC) was used to investigate the interactions of bile salts with phosphatidylcholine vesicles. We determined the partition coefficients of the detergents sodium cholate (NaC) and sodium deoxycholate (NaDC) and the respective transfer enthalpies between pure water or 0.1 M aqueous salt solution and bilayers, consisting of 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) and of 1,2-dimyristoyl-sn-glycero-3-phosphatidylcholine (DMPC). Additionally, the vesicle-to-micelle transition was investigated for NaC/DPPC and NaDC/DPPC systems in water and 0.1 M NaCl. ITC was employed to determine the phase boundaries for the saturation and the complete solubilization of the vesicles by the bile salts enclosing the coexistence region of mixed vesicles and micelles. To study the influence of the alkyl chain length of the phospholipids on the phase behavior we also studied the NaDC/ DMPC system. Saturated phosphatidylcholines are more easily transformed into micelles than those with unsaturated chains. In the region of low lipid concentrations we observed a departure from linearity of the phase boundaries, which was explained by the influence of the energy of end-caps as proposed by Roth et al. (Langmuir 2000(Langmuir , 16, 2052. The deviation was larger for systems in pure water compared to those in 0.1 M NaCl. The saturation concentrations of bilayers of DPPC and DMPC were much lower than those for unsaturated analogues. The saturation concentration increased with increasing salt content, and the coexistence range became wider. The ITC solubilization curves could be analyzed by applying the known values for partition coefficients and transfer enthalpies for the detergents to the different types of aggregates.

Abstract:The two main steps of the membranolytic activity of detergents: 1) the partitioning of detergent molecules in the membrane and 2) the solubilisation of the membrane are systematically investigated. The interactions of two bile salt molecules, sodium cholate (NaC) and sodium deoxycholate (NaDC) with biological phospholipid model membranes are considered. The membranolytic activity is analysed as a function of the hydrophobicity of the bile salt, ionic strength, temperature, membrane phase properties, membrane surface charge and composition of the acyl chains of the lipids. The results are derived from calorimetric measurements (ITC, isothermal titration calorimetry). A thermodynamic model is described, taking into consideration electrostatic interactions, which is used for the calculation of the partition coefficient as well as to derive the complete thermodynamic parameters describing the interaction of detergents with biological membranes (change in enthalpy, change in free energy, change in entropy etc). The solubilisation properties are described in a so-called vesicle-to-micelle phase transition diagram. The obtained results are supplemented and confirmed by data obtained from other biophysical techniques (DSC differential scanning calorimetry, DLS dynamic light scattering, SANS small angle neutron scattering).

Isothermal titration calorimetry (ITC) was used to determine the critical micelle concentration (cmc) and the thermodynamic parameters associated with the demicellization of sodium oleate (NaO) and mixed micelles composed of the bile salt (BS) sodium cholate (NaC) or sodium deoxycholate (NaDC), respectively, and NaO at a molar ratio of 5:2. The influence of the ionic strength (pure water and 0.1 M NaCl at pH 7.5) as well as that of the temperature (10-70 degrees C) were analyzed. For NaO, two cmc's were detected, indicating a two-step aggregation process, whereas only one cmc was observed for the two BSs. A single aggregation mechanism is also evident for the demicellization of mixed micelles (BS/NaO 5:2). Increasing the ionic strength induces the well-known decrease of the cmc. The cmc shows a minimum at room temperature. The cmc(mix) of the mixed micelles was analyzed using models assuming an ideal or nonideal mixing behavior of both detergents. The thermodynamic parameters describing the enthalpy (deltaHdemic), entropy (deltaSdemic), and Gibbs energy change (deltaGdemic), as well as the change in heat capacity (deltaCp,demic) for demicellization, were obtained from one ITC experiment. From the temperature dependence of deltaHdemic, the change of the hydrophobic surface area of the detergents from the micellar into the aqueous phase was derived. In all cases, the deltaCp,demic values are positive. In addition, the temperature dependence of the size of the formed aggregates was studied by dynamic light scattering (DLS). DLS indicated two populations of aggregates in the mixed system, small primary micelles (0.5-2 nm), and larger aggregates with a hydrodynamic radius in the range of 50-150 nm.

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