AVS 55th International Symposium & Exhibition | |
Surface Science | Thursday Sessions |
Session SS-ThP |
Session: | Poster Session |
Presenter: | C. Franqui, Smith College |
Authors: | C. Franqui, Smith College H. Applebaum, Smith College K.T. Queeney, Smith College |
Correspondent: | Click to Email |
The poly-L-lysine (PLL)-mediated adsorption of alginate to hydrophobic and hydrophilic substrates is a useful model system for understanding the initial stages of biofilm formation. Work in our lab using a variety of techniques has shown that film continuity and morphology are strongly influenced by the underlying substrate. The current work uses atomic force microscopy (AFM) to examine differences in film morphology as a function both of substrate surface chemistry and of adsorption conditions. On a hydrophobic, electrically neutral alkylsilane monolayer, PLL films adsorbed from pH 11 buffer and air dried exhibit morphologies that are suggestive of polymer shrinking as water is removed from the film, with networks of PLL surrounding regularly-spaced patches of bare surface. The proportion of surface covered by PLL decreases with increasing PLL molecular weight, which suggests stronger PLL-surface interactions for the lower MW polymers. Since adsorption under these conditions is thought to be driven by a transition from alpha helix in solution to random coil for adsorbed PLL, these results may indicated a lesser amount of uncoiling for the larger MW PLL. The role of drying in determining film morphologies is explored by comparing subsequently-adsorbed alginate films on both pre-dried and undried PLL overlayers. On hydrophilic silica PLL adsorbed at neutral pH forms much more uniform films, consistent with strong electrostatic interactions between the positively charged PLL and the negatively charged surface. As ionic strength increases, PLL begins to aggregate on the surface to form a much more discontinuous film, consistent with competition for binding sites between PLL and cations in solution. Alginate adsorption to these PLL overlayers results in more complex morphologies indicative more of isolated molecular adsorption than of true film formation.