Penetration and saturation of lysozyme in phospholipid bilayers.

We show that the combination of X-ray reflectivity, tryptophan fluorescence spectrum, and fluorescence quenching by bromine provides a useful tool to probe the location of lysozyme in lipid bilayers. To this end, we prepare lamellar complexes composed of phospholipids and lysozyme on solid surfaces using a solution-casting method. The proteins lie spontaneously between adjacent bilayers in the complexes. The results indicate that lysozyme may penetrate into the lipid bilayers. But the penetration depth is very shallow, and the tryptophan residues do not penetrate beyond the interface between the hydrocardon core and the headgroup region of the lipid bilayer. The penetration becomes saturated when more proteins are incorporated into the lamellar complex. The excess proteins stay in the interlamellar aqueous layers.

Electrochemical growth of highly oriented organic-inorganic superlattices using solid-supported multilamellar membranes as templates.

Controllable depositing of relatively thick inorganic sublayers into organic templates to fabricate organic-inorganic superlattices is of great importance. We report a novel approach to fabricating phospholipid/Ni(OH)(2) superlattices by electrochemical deposition of the inorganic component into solid-supported multilamellar templates. The well-ordered and highly oriented multilamellar templates are produced by spreading small drops of lipid solution on silicon surfaces and letting the solvent evaporate slowly. The templates which are used as working electrodes preserve the lamellar structure in the electrolyte solution. The resulting superlattices are highly oriented. The thickness of the nickel hydroxide is controlled by the concentration of nickel ions in the electrolyte bath. The electron density profiles derived from the X-ray diffraction data reveal that the thickness of the nickel hydroxide sublayers increases from 15 to 27 A as the concentration of nickel nitrate increases from 0.005 mol/L to 0.08 mol/L. We expect that the new method can be extended to depositing a variety of inorganic components including metals, oxides, and semiconductors.

Temperature dependence of interfacial fluctuations of polymerized fatty acid salt multilayers.

X-ray scattering was used to study the temperature dependence of the profile structure of polymerized 10,12-tricosadiynoic acid salt multilayers. The stacking periodicity of the multilayers was found to decrease with increasing temperature due to the conformational changes of the alkyl chains. When the samples were fully hydrated in water, the reflectivity measurement showed that the thermal fluctuations of the interfaces are enhanced with temperature, resulting in reduced ordering. Meanwhile, the diffuse scattering indicated that the thermal fluctuations renormalize the elasticity of the multilayers; both the bending and the compression moduli are reduced. Similar measurements performed in air, however, do not show this thermal enhancement although the stacking periodicity decreases in the same manner. It is implied that water might weaken the interaction between the carboxyl groups and the metal ions so that the polymerized bilayers are softened in water.

Electrochemical self-assembly of highly oriented ZnO-surfactant hybrid multilayers.

Highly oriented zinc oxide-surfactant hybrid multilayers were electrochemically self-assembled on silicon substrates from Zn(NO3)2 solutions containing extremely low concentration of sodium dodecyl sulfate (SDS). The X-ray diffraction results showed that the structure of the hybrid film is sensitive to the concentration of SDS. When the concentration of SDS is below a critical value, 0.002 wt %, a surfactant bilayer is adsorbed on the silicon surface, together with electrodeposited crystalline ZnO particles. Above this concentration, lamellar ZnO-surfactant hybrid films are formed, the period of which decreases from 31.7 +/- 0.2 A at 0.003 wt % to 27.5 +/- 0.2 A at 0.005 wt %, another critical concentration. It then increases monotonically and reaches its maximum of 33.0 +/- 0.2 A above 0.05 wt %. The results implied that the kinetics of the electrochemical self-assembly depends on the relative speed of the reduction of the zinc ions and the aggregation of the surfactant. The two processes occur cooperatively at the electrolyte-electrode interface to form the hybrid films.