Effects of temperature and pH on the helicity of a peptide adsorbed to colloidal silica.

The conformation of a cationic alpha-helical peptide (DDDDAAAARRRRR) adsorbed to anionic colloidal silica has been investigated by circular dichroism (CD) spectroscopy as a function of temperature and pH in order to examine how the structure of an adsorbed molecule responds to two simultaneous perturbations. Increased temperature destabilizes the helicity of the peptide in solution, while pH changes alter the substrate surface charge and the corresponding strength of the interaction with the peptide. Near neutral pH, the helicity of the adsorbed peptide, which is determined from the intensity of the CD signal at 222 nm, decreases with increasing temperature, similarly to the temperature-dependent behavior observed for the peptide in aqueous solution. By contrast, at basic pH and a strongly negative surface charge, the helicity of the adsorbed peptide increases with temperature. In order to elucidate the origin of the reversal of the temperature dependence of helicity, a statistical model for the conformation of the adsorbed peptide has been formulated based on the Lifson-Roig model for the helix-coil transition of the peptide in solution. The model provides insight into the trends in fractional helicity and reveals that the temperature dependence of the helicity of the adsorbed peptide results from a competition between the intramolecular interactions that promote helicity and the intermolecular interactions with the surface. The statistical model also enables estimation of the free energy contributions from specific aspects of the adsorption process. Through identification of a connection between the conformation of adsorbed peptide and the interactions of the peptide with the surface, this work suggests a route for the control of adsorbate conformation through peptide and surface engineering.

Asymmetric alpha-helicity loss within a peptide adsorbed onto charged colloidal substrates.

A combination of circular dichroism and solution 1H NMR spectroscopy provides a localized description of the distribution of alpha -helical structure within the capped peptide DDDDAAAAARRRR (4DAR5) in aqueous solution and adsorbed onto anionic and cationic colloidal substrates. The adsorption-induced conformational changes are different from those observed upon heating 4DAR5 in solution, in which case the alanine segment remains largely alpha -helical and the transition to a coil structure propagates from the termini. Adsorption is driven by electrostatic complementarity, which places the charged peptide segment adjacent to the substrate of opposite charge. A similar pattern of alpha -helicity loss is observed whether the peptide is adsorbed onto anionic or cationic colloidal silica, despite inverse orientations; significant alpha -helicity loss occurs within the central alanine segment and the terminal arginine segment, whereas alpha -helicity is retained in the aspartate segment. This pattern of adsorption-induced conformational change illustrates the complex and subtle balance among the intramolecular and intermolecular factors that influence the conformations of adsorbed peptides and proteins.