Issue 23, 2006

Proteinadsorption on the hydrophilic surface of a glassy polymer: a computer simulation study

Abstract

Using atomistic computer simulations, we study the adsorption of different globular protein fragments with different secondary structures on the surface of a hydrophilic glassy polymer, poly(vinyl alcohol), or PVA, and compare the results with our earlier calculations on hydrophobic graphite. The simulations were mainly carried out with implicit solvent in an effective dielectric medium by energy minimizations and molecular dynamics at room temperature. We find that on the hydrophilic PVA surface the fragments basically retain their globular shape with an incomplete denaturation, at variance with our earlier results for the same fragments on graphite. Correspondingly, the interaction energy between the fragments and the surface is significantly smaller than on graphite, both because less residues are in contact with the surface, and because they interact more weakly. Moreover, very few hydrogen bonds are formed between the adsorbate and the PVA surface, since both the protein fragments and the polymer chains separately optimize these interactions. Additional molecular dynamics simulations in explicit solvent were also performed to study the hydration of the adsorbed fragments and to estimate the possible solvation effects.

Graphical abstract: Protein adsorption on the hydrophilic surface of a glassy polymer: a computer simulation study

Article information

Article type
Paper
Submitted
28 Mar 2006
Accepted
08 May 2006
First published
19 May 2006

Phys. Chem. Chem. Phys., 2006,8, 2765-2772

Protein adsorption on the hydrophilic surface of a glassy polymer: a computer simulation study

G. Raffaini and F. Ganazzoli, Phys. Chem. Chem. Phys., 2006, 8, 2765 DOI: 10.1039/B604540E

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