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Air Filter Devices Including Nonwoven Meshes of Electrospun Recombinant Spider Silk Proteins

Based on the natural sequence of Araneus diadematus Fibroin 4 (ADF4), the recombinant spider silk protein eADF4(C16) has been engineered. This highly repetitive protein has a molecular weight of 48kDa and is soluble in different solvents (hexafluoroisopropanol (HFIP), formic acid and aqueous buffers...

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Autores principales: Lang, Gregor, Jokisch, Stephan, Scheibel, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679617/
https://www.ncbi.nlm.nih.gov/pubmed/23685883
http://dx.doi.org/10.3791/50492
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author Lang, Gregor
Jokisch, Stephan
Scheibel, Thomas
author_facet Lang, Gregor
Jokisch, Stephan
Scheibel, Thomas
author_sort Lang, Gregor
collection PubMed
description Based on the natural sequence of Araneus diadematus Fibroin 4 (ADF4), the recombinant spider silk protein eADF4(C16) has been engineered. This highly repetitive protein has a molecular weight of 48kDa and is soluble in different solvents (hexafluoroisopropanol (HFIP), formic acid and aqueous buffers). eADF4(C16) provides a high potential for various technical applications when processed into morphologies such as films, capsules, particles, hydrogels, coatings, fibers and nonwoven meshes. Due to their chemical stability and controlled morphology, the latter can be used to improve filter materials. In this protocol, we present a procedure to enhance the efficiency of different air filter devices, by deposition of nonwoven meshes of electrospun recombinant spider silk proteins. Electrospinning of eADF4(C16) dissolved in HFIP results in smooth fibers. Variation of the protein concentration (5-25% w/v) results in different fiber diameters (80-1,100 nm) and thus pore sizes of the nonwoven mesh. Post-treatment of eADF4(C16) electrospun from HFIP is necessary since the protein displays a predominantly α-helical secondary structure in freshly spun fibers, and therefore the fibers are water soluble. Subsequent treatment with ethanol vapor induces formation of water resistant, stable β-sheet structures, preserving the morphology of the silk fibers and meshes. Secondary structure analysis was performed using Fourier transform infrared spectroscopy (FTIR) and subsequent Fourier self-deconvolution (FSD). The primary goal was to improve the filter efficiency of existing filter substrates by adding silk nonwoven layers on top. To evaluate the influence of electrospinning duration and thus nonwoven layer thickness on the filter efficiency, we performed air permeability tests in combination with particle deposition measurements. The experiments were carried out according to standard protocols.
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spelling pubmed-36796172013-06-13 Air Filter Devices Including Nonwoven Meshes of Electrospun Recombinant Spider Silk Proteins Lang, Gregor Jokisch, Stephan Scheibel, Thomas J Vis Exp Bioengineering Based on the natural sequence of Araneus diadematus Fibroin 4 (ADF4), the recombinant spider silk protein eADF4(C16) has been engineered. This highly repetitive protein has a molecular weight of 48kDa and is soluble in different solvents (hexafluoroisopropanol (HFIP), formic acid and aqueous buffers). eADF4(C16) provides a high potential for various technical applications when processed into morphologies such as films, capsules, particles, hydrogels, coatings, fibers and nonwoven meshes. Due to their chemical stability and controlled morphology, the latter can be used to improve filter materials. In this protocol, we present a procedure to enhance the efficiency of different air filter devices, by deposition of nonwoven meshes of electrospun recombinant spider silk proteins. Electrospinning of eADF4(C16) dissolved in HFIP results in smooth fibers. Variation of the protein concentration (5-25% w/v) results in different fiber diameters (80-1,100 nm) and thus pore sizes of the nonwoven mesh. Post-treatment of eADF4(C16) electrospun from HFIP is necessary since the protein displays a predominantly α-helical secondary structure in freshly spun fibers, and therefore the fibers are water soluble. Subsequent treatment with ethanol vapor induces formation of water resistant, stable β-sheet structures, preserving the morphology of the silk fibers and meshes. Secondary structure analysis was performed using Fourier transform infrared spectroscopy (FTIR) and subsequent Fourier self-deconvolution (FSD). The primary goal was to improve the filter efficiency of existing filter substrates by adding silk nonwoven layers on top. To evaluate the influence of electrospinning duration and thus nonwoven layer thickness on the filter efficiency, we performed air permeability tests in combination with particle deposition measurements. The experiments were carried out according to standard protocols. MyJove Corporation 2013-05-08 /pmc/articles/PMC3679617/ /pubmed/23685883 http://dx.doi.org/10.3791/50492 Text en Copyright © 2013, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Bioengineering
Lang, Gregor
Jokisch, Stephan
Scheibel, Thomas
Air Filter Devices Including Nonwoven Meshes of Electrospun Recombinant Spider Silk Proteins
title Air Filter Devices Including Nonwoven Meshes of Electrospun Recombinant Spider Silk Proteins
title_full Air Filter Devices Including Nonwoven Meshes of Electrospun Recombinant Spider Silk Proteins
title_fullStr Air Filter Devices Including Nonwoven Meshes of Electrospun Recombinant Spider Silk Proteins
title_full_unstemmed Air Filter Devices Including Nonwoven Meshes of Electrospun Recombinant Spider Silk Proteins
title_short Air Filter Devices Including Nonwoven Meshes of Electrospun Recombinant Spider Silk Proteins
title_sort air filter devices including nonwoven meshes of electrospun recombinant spider silk proteins
topic Bioengineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679617/
https://www.ncbi.nlm.nih.gov/pubmed/23685883
http://dx.doi.org/10.3791/50492
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