Poly-acrylic Acid Brushes and Adsorbed Proteins

Author:

Reinhardt Matthias1,Kreuzer Martin1,Geue Thomas2,Dahint Reiner3,Ballauff Matthias1,Steitz Roland1

Affiliation:

1. Helmholtz-Zentrum Berlin, Institute of Soft Matter and Functional Materials, Hahn-Meitner-Platz 1, 14109 Berlin, Germany

2. Paul Scherrer Institut, Laboratory for Neutron Scattering, 5210 Villigen, Switzerland

3. Ruprecht-Karls-Universität Heidelberg, Applied Physical Chemistry, Im Neuenheimer Feld 253, 69120 Heidelberg, Germany

Abstract

Abstract Planar polyelectrolyte brushes are prepared by Langmuir–Schaefer based grafting of perdeuterated (styrene)49-b-(acrylic acid)222 block copolymer (dPS-b-PAA) to dPS pre-coated silicon supports with grafting density σ PAA from 0.07 to 0.11 nm 2. The structure of the solvent-swollen brushes, i. e. the volume fraction profile of polymer segments, ϕ PAA, as a function of altitude z from the grafting plane into the liquid phase is extracted from neutron reflectivity measurements. We find that for all cases investigated ϕ PAA(z) resembles a Gaussian profile. Although very condensed, the PAA brushes can be loaded with bovine serum albumin (BSA). The integral amount of adsorbed BSA scales linearly with grafting density. We compare our z-resolved volume fraction profile ϕ BSA(z) of BSA on PAA brushes with existing literature on that system. It is found that a cross-over takes place in the adsorption scheme from ternary compressive, where proteins can approach the grafting surface only by compressing the brush, to ternary insertive, where proteins enter the brush with only local perturbation of the concentration profile, as a function of R P/H max, where R P is the Stokes-Radius of the protein, and H max is the experimentally determined maximum height of the brush.

Publisher

Walter de Gruyter GmbH

Subject

Physical and Theoretical Chemistry

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