TY - JOUR
T1 - Highly Hydrophobic Films of Engineered Silk Proteins by a Simple Deposition Method
AU - Välisalmi, Teemu
AU - Roas-Escalona, Nelmary
AU - Meinander, Kristoffer
AU - Mohammadi, Pezhman
AU - Linder, Markus B.
N1 - Funding Information:
This work was funded by the Academy of Finland through Projects 317019 and 348628, the Center of Excellence Program (2022–2029) in Life-Inspired Hybrid Materials (LIBER) through Project 346105, and the Novo Nordisk Foundation (0061306).
PY - 2023/3/28
Y1 - 2023/3/28
N2 - 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.
AB - 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.
KW - Animals
KW - Silk/chemistry
KW - Water/chemistry
KW - Hydrophobic and Hydrophilic Interactions
KW - Wettability
KW - Spiders
KW - Recombinant Proteins/chemistry
UR - http://www.scopus.com/inward/record.url?scp=85150430934&partnerID=8YFLogxK
U2 - 10.1021/acs.langmuir.2c03442
DO - 10.1021/acs.langmuir.2c03442
M3 - Article
C2 - 36926896
SN - 0743-7463
VL - 39
SP - 4370
EP - 4381
JO - Langmuir
JF - Langmuir
IS - 12
ER -