Functional Modification of Silica through Enhanced Adsorption of Elastin-Like Polypeptide Block Copolymers.

TitleFunctional Modification of Silica through Enhanced Adsorption of Elastin-Like Polypeptide Block Copolymers.
Publication TypeJournal Article
Year of Publication2018
AuthorsL Li, NK Li, Q Tu, O Im, C-K Mo, W Han, WH Fuss, NJ Carroll, A Chilkoti, YG Yingling, S Zauscher, and GP López
JournalBiomacromolecules
Volume19
Issue2
Start Page298
Pagination298 - 306
Date Published02/2018
Abstract

A powerful tool for controlling interfacial properties and molecular architecture relies on the tailored adsorption of stimuli-responsive block copolymers onto surfaces. Here, we use computational and experimental approaches to investigate the adsorption behavior of thermally responsive polypeptide block copolymers (elastin-like polypeptides, ELPs) onto silica surfaces, and to explore the effects of surface affinity and micellization on the adsorption kinetics and the resultant polypeptide layers. We demonstrate that genetic incorporation of a silica-binding peptide (silaffin R5) results in enhanced adsorption of these block copolymers onto silica surfaces as measured by quartz crystal microbalance and ellipsometry. We find that the silaffin peptide can also direct micelle adsorption, leading to close-packed micellar arrangements that are distinct from the sparse, patchy arrangements observed for ELP micelles lacking a silaffin tag, as evidenced by atomic force microscopy measurements. These experimental findings are consistent with results of dissipative particle dynamics simulations. Wettability measurements suggest that surface immobilization hampers the temperature-dependent conformational change of ELP micelles, while adsorbed ELP unimers (i.e., unmicellized block copolymers) retain their thermally responsive property at interfaces. These observations provide guidance on the use of ELP block copolymers as building blocks for fabricating smart surfaces and interfaces with programmable architecture and functionality.

DOI10.1021/acs.biomac.7b01307
Short TitleBiomacromolecules