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Highly Hydrophobic Films of Engineered Silk Proteins by a Simple Deposition Method
[Image: see text] 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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061925/ https://www.ncbi.nlm.nih.gov/pubmed/36926896 http://dx.doi.org/10.1021/acs.langmuir.2c03442 |
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author | Välisalmi, Teemu Roas-Escalona, Nelmary Meinander, Kristoffer Mohammadi, Pezhman Linder, Markus B. |
author_facet | Välisalmi, Teemu Roas-Escalona, Nelmary Meinander, Kristoffer Mohammadi, Pezhman Linder, Markus B. |
author_sort | Välisalmi, Teemu |
collection | PubMed |
description | [Image: see text] 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. |
format | Online Article Text |
id | pubmed-10061925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100619252023-03-31 Highly Hydrophobic Films of Engineered Silk Proteins by a Simple Deposition Method Välisalmi, Teemu Roas-Escalona, Nelmary Meinander, Kristoffer Mohammadi, Pezhman Linder, Markus B. Langmuir [Image: see text] 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. American Chemical Society 2023-03-16 /pmc/articles/PMC10061925/ /pubmed/36926896 http://dx.doi.org/10.1021/acs.langmuir.2c03442 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Välisalmi, Teemu Roas-Escalona, Nelmary Meinander, Kristoffer Mohammadi, Pezhman Linder, Markus B. Highly Hydrophobic Films of Engineered Silk Proteins by a Simple Deposition Method |
title | Highly Hydrophobic
Films of Engineered Silk Proteins
by a Simple Deposition Method |
title_full | Highly Hydrophobic
Films of Engineered Silk Proteins
by a Simple Deposition Method |
title_fullStr | Highly Hydrophobic
Films of Engineered Silk Proteins
by a Simple Deposition Method |
title_full_unstemmed | Highly Hydrophobic
Films of Engineered Silk Proteins
by a Simple Deposition Method |
title_short | Highly Hydrophobic
Films of Engineered Silk Proteins
by a Simple Deposition Method |
title_sort | highly hydrophobic
films of engineered silk proteins
by a simple deposition method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061925/ https://www.ncbi.nlm.nih.gov/pubmed/36926896 http://dx.doi.org/10.1021/acs.langmuir.2c03442 |
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