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Protein detection enabled using functionalised silk-binding peptides on a silk-coated optical fibre
We present a new coating procedure to prepare optical fibre sensors suitable for use with protein analytes. We demonstrate this through the detection of AlexaFluor-532 tagged streptavidin by its binding to D-biotin that is functionalised onto an optical fibre, via incorporation in a silk fibroin fib...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034238/ https://www.ncbi.nlm.nih.gov/pubmed/35480827 http://dx.doi.org/10.1039/d1ra03584c |
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author | Capon, Patrick K. Horsfall, Aimee J. Li, Jiawen Schartner, Erik P. Khalid, Asma Purdey, Malcolm S. McLaughlin, Robert A. Abell, Andrew D. |
author_facet | Capon, Patrick K. Horsfall, Aimee J. Li, Jiawen Schartner, Erik P. Khalid, Asma Purdey, Malcolm S. McLaughlin, Robert A. Abell, Andrew D. |
author_sort | Capon, Patrick K. |
collection | PubMed |
description | We present a new coating procedure to prepare optical fibre sensors suitable for use with protein analytes. We demonstrate this through the detection of AlexaFluor-532 tagged streptavidin by its binding to D-biotin that is functionalised onto an optical fibre, via incorporation in a silk fibroin fibre coating. The D-biotin was covalently attached to a silk-binding peptide to provide SBP–biotin, which adheres the D-biotin to the silk-coated fibre tip. These optical fibre probes were prepared by two methods. The first involves dip-coating the fibre tip into a mixture of silk fibroin and SBP–biotin, which distributes the SBP–biotin throughout the silk coating (method A). The second method uses two steps, where the fibre is first dip-coated in silk only, then SBP–biotin added in a second dip-coating step. This isolates SBP–biotin to the outer surface of the silk layer (method B). A series of fluorescence measurements revealed that only the surface bound SBP–biotin detects streptavidin with a detection limit of 15 μg mL(−1). The fibre coatings are stable to repeated washing and long-term exposure to water. Formation of silk coatings on fibres using commercial aqueous silk fibroin was found to be inhibited by a lithium concentration of 200 ppm, as determined by atomic absorption spectroscopy. This was reduced to less than 20 ppm by dialysis against water, and was found to successfully form a coating on optical fibres. |
format | Online Article Text |
id | pubmed-9034238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90342382022-04-26 Protein detection enabled using functionalised silk-binding peptides on a silk-coated optical fibre Capon, Patrick K. Horsfall, Aimee J. Li, Jiawen Schartner, Erik P. Khalid, Asma Purdey, Malcolm S. McLaughlin, Robert A. Abell, Andrew D. RSC Adv Chemistry We present a new coating procedure to prepare optical fibre sensors suitable for use with protein analytes. We demonstrate this through the detection of AlexaFluor-532 tagged streptavidin by its binding to D-biotin that is functionalised onto an optical fibre, via incorporation in a silk fibroin fibre coating. The D-biotin was covalently attached to a silk-binding peptide to provide SBP–biotin, which adheres the D-biotin to the silk-coated fibre tip. These optical fibre probes were prepared by two methods. The first involves dip-coating the fibre tip into a mixture of silk fibroin and SBP–biotin, which distributes the SBP–biotin throughout the silk coating (method A). The second method uses two steps, where the fibre is first dip-coated in silk only, then SBP–biotin added in a second dip-coating step. This isolates SBP–biotin to the outer surface of the silk layer (method B). A series of fluorescence measurements revealed that only the surface bound SBP–biotin detects streptavidin with a detection limit of 15 μg mL(−1). The fibre coatings are stable to repeated washing and long-term exposure to water. Formation of silk coatings on fibres using commercial aqueous silk fibroin was found to be inhibited by a lithium concentration of 200 ppm, as determined by atomic absorption spectroscopy. This was reduced to less than 20 ppm by dialysis against water, and was found to successfully form a coating on optical fibres. The Royal Society of Chemistry 2021-06-24 /pmc/articles/PMC9034238/ /pubmed/35480827 http://dx.doi.org/10.1039/d1ra03584c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Capon, Patrick K. Horsfall, Aimee J. Li, Jiawen Schartner, Erik P. Khalid, Asma Purdey, Malcolm S. McLaughlin, Robert A. Abell, Andrew D. Protein detection enabled using functionalised silk-binding peptides on a silk-coated optical fibre |
title | Protein detection enabled using functionalised silk-binding peptides on a silk-coated optical fibre |
title_full | Protein detection enabled using functionalised silk-binding peptides on a silk-coated optical fibre |
title_fullStr | Protein detection enabled using functionalised silk-binding peptides on a silk-coated optical fibre |
title_full_unstemmed | Protein detection enabled using functionalised silk-binding peptides on a silk-coated optical fibre |
title_short | Protein detection enabled using functionalised silk-binding peptides on a silk-coated optical fibre |
title_sort | protein detection enabled using functionalised silk-binding peptides on a silk-coated optical fibre |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034238/ https://www.ncbi.nlm.nih.gov/pubmed/35480827 http://dx.doi.org/10.1039/d1ra03584c |
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