Abstract
A technique is described and demonstrated for measuring the orientation distribution of fluorescent molecules in a two-dimensional system. A laser beam is totally internally reflected at the interface between a glass slide and an aqueous solution, which creates a thin layer of evanescent illumination that excites fluorescent molecules near the interface. Molecules with absorption dipoles at different tilts from the normal to the interface are preferentially excited when the laser polarization is rotated. Approximately one-half of the emitted fluorescence is collected with an inverted microscope using a high-aperture objective. The fluorescence vs. polarization curve yields the value of an order parameter that is related to the orientation distribution of absorption dipoles. This technique is applied to phospholipid monolayers made at an air/water interface and transferred to hydrophobic glass microscope slides. Dipalmitoylphosphatidylcholine monolayers were doped with 2 mol% phosphatidylethanolamine labeled with the fluorescent moiety nitrobenzoxadiazole, either on an acyl chain or on the head group. The measured value of the order parameter for the head-labeled probe decreases as a function of the surface pressure at which the monolayer is transferred to the slide, as the surface pressure increases from 10 to 40 dyne/cm. The measured value of the order parameter for the chain-labeled probe is high for all coating pressures. These results can be interpreted in terms of probe partitioning into coexistent fluid and solid domains. Dimyristoylphosphatidylcholine monolayers were doped with 2 mol% chain-labeled phosphatidylethanolamine, either free or covalently conjugated to a small peptide. In these monolayers, the measured value of the order parameter is high at all pressures. The technique presented here may also prove useful for measuring the orientation distribution of proteins bound to or embedded in a planar model membrane.