Protein Orientation and Polymer Phase Separation Induced by Poly(methyl methacrylate) Tacticity

Abstract

Stereochemistry may affect the physicochemical and biological properties of polymer films that are important for their applications, including substrates for the fabrication of protein microarrays. In this study, we investigated the effect of poly(methyl methacrylate) (PMMA) tacticity on the interaction of polymer thin films with proteins and on the phase separation process in blends with poly(tert-butyl methacrylate) (PtBMA). Thin films of isotactic, atactic, and syndiotactic PMMA were studied for topography, surface chemistry, and protein adsorption. Secondary ion mass spectrometry and contact angle measurements revealed a lower surface exposure of polar ester functional groups for iso-PMMA, resulting in the reduced adsorption of albumin and fibrinogen proteins. We also showed that changes in surface chemistry alter the orientation of proteins adsorbed on iso-PMMA through hydrophobic and electrostatic interactions. In addition, blends composed of PMMA and PtBMA, both of different tacticities, were investigated in terms of protein microarray fabrication. The two-dimensional domain structure was obtained by a phase separation process for at-PtBMA blends prepared on silicon substrates modified with amino-silane. Finally, for an isotropic and regular polymer pattern of iso-PMMA/at-PtBMA, the possibility of protein microarray formation on this blend was demonstrated, showing selective adsorption to PtBMA domains and perfect mirroring of the polymer patterns.