The surface of oxygen-plasma-treated polystyrene (PSox) was investigated using X-ray photoelectron
spectroscopy (XPS), streaming potential measurements and a dynamic study of the wetting properties at
different pH (Wilhelmy plate method). The PSox surface is functionalized with various oxygen-containing
groups, including carboxyl functions, and must be viewed as covered by a polyelectrolyte which swells
depending on pH. The wetting hysteresis, its evolution upon repeated cycles and the influence of pH are
controlled by the dissolution of functionalized fragments and the retention of water upon emersion; the
retained water may evaporate progressively and allow macromolecule compaction and/or reorientation.
Modification of the PSox surface upon aging in dry atmosphere, humid atmosphere, and water was studied
using XPS and dynamic wetting measurements. Aging in water provoked the dissolution of PSox
macromolecular chains, as indicated by adsorption of released fragments on a check PS sample placed
nearby. However, the concentration of functionalized molecules at the surface of water-aged PSox was still
sufficient to allow swelling at pH 5.6 and 11.0. Hydrophobicity recovery was faster in humid air (R. H.
95%) compared to dry air (R. H. 5%), due to the plasticizing effect of water. Hydrophobicity recovery upon
aging in air was reversed quickly by immersion at pH 5.6 or 11.0, due to deprotonation and swelling.
We used atomic force microscopy (AFM) to explore the antigen binding forces of individual Fv fragments of antilysozyme antibodies (Fv). To detect single molecular recognition events, genetically engineered histidine-tagged Fv fragments were coupled onto AFM tips modified with mixed self-assembled monolayers (SAMs) of nitrilotriacetic acid- and tri(ethylene glycol)-terminated alkanethiols while lysozyme (Lyso) was covalently immobilized onto mixed SAMs of carboxyl- and hydroxyl-terminated alkanethiols. The quality of the functionalization procedure was validated using X-ray photoelectron spectroscopy (surface chemical composition), AFM imaging (surface morphology in aqueous solution), and surface plasmon resonance (SPR, specific binding in aqueous solution). AFM force-distance curves recorded at a loading rate of 5000 pN/s between Fv- and Lyso-modified surfaces yielded a distribution of unbinding forces composed of integer multiples of an elementary force quantum of approximately 50 pN that we attribute to the rupture of a single antibody-antigen pair. Injection of a solution containing free Lyso caused a dramatic reduction of adhesion probability, indicating that the measured 50 pN unbinding forces are due to the specific antibody-antigen interaction. To investigate the dynamics of the interaction, force-distance curves were recorded at various loading rates. Plots of unbinding force vs log(loading rate) revealed two distinct linear regimes with ascending slopes, indicating multiple barriers were present in the energy landscape. The kinetic off-rate constant of dissociation (k(off) approximately = 1 x 10(-3) s(-1)) obtained by extrapolating the data of the low-strength regime to zero force was in the range of the k(off) estimated by SPR.
The concentrations of elements or functions ratioed to total carbon can be modeled on the basis of the known composition of model biochemical compounds, which leads to an evaluation of the surface composition expressed in wt% of these classes of compounds. Thereby, it was shown that surface accumulation, as compared to the bulk, increases in the order proteins < NL < PL. Moreover, the surface enrichment of PL compared to triglycerides was found to be increased after baking.
Mixed monolayers of the surface-active lipopeptide surfactin-C(15) and of dipalmitoyl phosphatidylcholine (DPPC) were deposited on mica and their nanometer scale organization was investigated using atomic force microscopy (AFM) and x-ray photoelectron spectroscopy (XPS). AFM topographic images revealed phase separation for mixed monolayers prepared at 0.1, 0.25, and 0.5 surfactin molar ratios. This was in agreement with the monolayer properties at the air-water interface indicating a tendency of the two compounds to form bidimensional domains in the mixed systems. The step height measured between the surfactin and the DPPC domains was 1.2 +/- 0.1 nm, pointing to a difference in molecular orientation: while DPPC had a vertical orientation, the large peptide ring of surfactin was lying on the mica surface. The N/C atom concentration ratios obtained by XPS for pure monolayers were compatible with two distinct geometric models: a random layer for surfactin and for DPPC, a layer of vertically-oriented molecules in which the polar headgroups are in contact with mica. XPS data for mixed systems were accounted for by a combination of the two pure monolayers, considering respective surface coverages that were in excellent agreement with those measured by AFM. These results illustrate the complementarity of AFM and XPS to directly probe the molecular organization of multicomponent monolayers.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.