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Highly Hydrophobic Films of Engineered Silk Proteins by a Simple Deposition Method.
Välisalmi, Teemu; Roas-Escalona, Nelmary; Meinander, Kristoffer; Mohammadi, Pezhman; Linder, Markus B.
Afiliação
  • Välisalmi T; Department of Bioproducts and Biosystems, School of Chemical Engineering, Aalto University, FI-00076 Aalto, Finland.
  • Roas-Escalona N; Centre of Excellence in Life-Inspired Hybrid Materials (LIBER), Aalto University, Post Office Box 16100, 00076 Aalto, Finland.
  • Meinander K; Department of Bioproducts and Biosystems, School of Chemical Engineering, Aalto University, FI-00076 Aalto, Finland.
  • Mohammadi P; Centre of Excellence in Life-Inspired Hybrid Materials (LIBER), Aalto University, Post Office Box 16100, 00076 Aalto, Finland.
  • Linder MB; Department of Bioproducts and Biosystems, School of Chemical Engineering, Aalto University, FI-00076 Aalto, Finland.
Langmuir ; 39(12): 4370-4381, 2023 03 28.
Article em En | MEDLINE | ID: mdl-36926896
ABSTRACT
Molecular engineering of protein structures offers a uniquely versatile route for novel functionalities in materials. Here, we describe a method to form highly hydrophobic thin films using genetically engineered spider silk proteins. We used structurally engineered protein variants containing ADF3 and AQ12 spider silk sequences. Wetting properties were studied using static and dynamic contact angle measurements. Solution conditions and the surrounding humidity during film preparation were key parameters to obtain high hydrophobicity, as shown by contact angles in excess of 120°. Although the surface layer was highly hydrophobic, its structure was disrupted by the added water droplets. Crystal-like structures were found at the spots where water droplets had been placed. To understand the mechanism of film formation, different variants of the proteins, the topography of the films, and secondary structures of the protein components were studied. The high contact angle in the films demonstrates that the conformations that silk proteins take in the protein layer very efficiently expose their hydrophobic segments. This work reveals a highly amphiphilic nature of silk proteins and contributes to an understanding of their assembly mechanisms. It will also help in designing diverse technical uses for recombinant silk.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article