Jump to main content
Jump to site search

Volume 191, 2016
Previous Article Next Article

Surface heterogeneity: a friend or foe of protein adsorption – insights from theoretical simulations

Author affiliations


A lack in the detailed understanding of mechanisms through which proteins adsorb or are repelled at various solid/liquid interfaces limits the capacity to rationally design and produce more sophisticated surfaces with controlled protein adsorption in both biomedical and industrial settings. To date there are three main approaches to achieve anti biofouling efficacy, namely chemically adjusting the surface hydrophobicity and introducing various degrees of surface roughness, or a combination of both. More recently, surface nanostructuring has been shown to have an effect on protein adsorption. However, the current resolution of experimental techniques makes it difficult to investigate these three phase systems at the molecular level. In this molecular dynamics study we explore in all-atom detail the adsorption process of one of the most surface active proteins, EAS hydrophobin, known for its versatile ability to self-assemble on both hydrophobic and hydrophilic surfaces forming stable monolayers that facilitate further biofilm growth. We model the adsorption of this protein on organic ligand protected silica surfaces with varying degrees of chemical heterogeneity and roughness, including fully homogenous hydrophobic and hydrophilic surfaces for comparison. We present a detailed characterisation of the functionalised surface structure and dynamics for each of these systems, and the effect the ligands have on interfacial water, the adsorption process and conformational rearrangements of the protein. Results suggest that the ligand arrangement that produces the highest hydrophilic chain mobility and the lack of significant hydrophobic patches shows the most promising anti-fouling efficacy toward hydrophobin. However, the presence on the protein surface of a flexible loop with amphipathic character (the Cys3–Cys4 loop) is seen to facilitate EAS adsorption on all surfaces by enabling the protein to match the surface pattern.

Back to tab navigation

Publication details

The article was received on 15 Mar 2016, accepted on 08 Apr 2016 and first published on 08 Apr 2016

Article type: Paper
DOI: 10.1039/C6FD00050A
Faraday Discuss., 2016,191, 435-464

  •   Request permissions

    Surface heterogeneity: a friend or foe of protein adsorption – insights from theoretical simulations

    M. Penna, K. Ley, S. Maclaughlin and I. Yarovsky, Faraday Discuss., 2016, 191, 435
    DOI: 10.1039/C6FD00050A

Search articles by author