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Silk fibroin as an additive for cell-free protein synthesis

Cell-free systems contain many proteins and metabolites required for complex functions such as transcription and translation or multi-step metabolic conversions. Research into expanding the delivery of these systems by drying or by embedding into other materials is enabling new applications in sensi...

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Autores principales: Lee, Marilyn S., Hung, Chia-Suei, Phillips, Daniel A., Buck, Chelsea C., Gupta, Maneesh K., Lux, Matthew W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320238/
https://www.ncbi.nlm.nih.gov/pubmed/32637668
http://dx.doi.org/10.1016/j.synbio.2020.06.004
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author Lee, Marilyn S.
Hung, Chia-Suei
Phillips, Daniel A.
Buck, Chelsea C.
Gupta, Maneesh K.
Lux, Matthew W.
author_facet Lee, Marilyn S.
Hung, Chia-Suei
Phillips, Daniel A.
Buck, Chelsea C.
Gupta, Maneesh K.
Lux, Matthew W.
author_sort Lee, Marilyn S.
collection PubMed
description Cell-free systems contain many proteins and metabolites required for complex functions such as transcription and translation or multi-step metabolic conversions. Research into expanding the delivery of these systems by drying or by embedding into other materials is enabling new applications in sensing, point-of-need manufacturing, and responsive materials. Meanwhile, silk fibroin from the silk worm, Bombyx mori, has received attention as a protective additive for dried enzyme formulations and as a material to build biocompatible hydrogels for controlled localization or delivery of biomolecular cargoes. In this work, we explore the effects of silk fibroin as an additive in cell-free protein synthesis (CFPS) reactions. Impacts of silk fibroin on CFPS activity and stability after drying, as well as the potential for incorporation of CFPS into hydrogels of crosslinked silk fibroin are assessed. We find that simple addition of silk fibroin increased productivity of the CFPS reactions by up to 42%, which we attribute to macromolecular crowding effects. However, we did not find evidence that silk fibroin provides a protective effects after drying as previously described for purified enzymes. Further, the enzymatic crosslinking transformations of silk fibroin typically used to form hydrogels are inhibited in the presence of the CFPS reaction mixture. Crosslinking attempts did not impact CFPS activity, but did yield localized protein aggregates rather than a hydrogel. We discuss the mechanisms at play in these results and how the silk fibroin-CFPS system might be improved for the design of cell-free devices.
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spelling pubmed-73202382020-07-06 Silk fibroin as an additive for cell-free protein synthesis Lee, Marilyn S. Hung, Chia-Suei Phillips, Daniel A. Buck, Chelsea C. Gupta, Maneesh K. Lux, Matthew W. Synth Syst Biotechnol Article Cell-free systems contain many proteins and metabolites required for complex functions such as transcription and translation or multi-step metabolic conversions. Research into expanding the delivery of these systems by drying or by embedding into other materials is enabling new applications in sensing, point-of-need manufacturing, and responsive materials. Meanwhile, silk fibroin from the silk worm, Bombyx mori, has received attention as a protective additive for dried enzyme formulations and as a material to build biocompatible hydrogels for controlled localization or delivery of biomolecular cargoes. In this work, we explore the effects of silk fibroin as an additive in cell-free protein synthesis (CFPS) reactions. Impacts of silk fibroin on CFPS activity and stability after drying, as well as the potential for incorporation of CFPS into hydrogels of crosslinked silk fibroin are assessed. We find that simple addition of silk fibroin increased productivity of the CFPS reactions by up to 42%, which we attribute to macromolecular crowding effects. However, we did not find evidence that silk fibroin provides a protective effects after drying as previously described for purified enzymes. Further, the enzymatic crosslinking transformations of silk fibroin typically used to form hydrogels are inhibited in the presence of the CFPS reaction mixture. Crosslinking attempts did not impact CFPS activity, but did yield localized protein aggregates rather than a hydrogel. We discuss the mechanisms at play in these results and how the silk fibroin-CFPS system might be improved for the design of cell-free devices. KeAi Publishing 2020-06-24 /pmc/articles/PMC7320238/ /pubmed/32637668 http://dx.doi.org/10.1016/j.synbio.2020.06.004 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Lee, Marilyn S.
Hung, Chia-Suei
Phillips, Daniel A.
Buck, Chelsea C.
Gupta, Maneesh K.
Lux, Matthew W.
Silk fibroin as an additive for cell-free protein synthesis
title Silk fibroin as an additive for cell-free protein synthesis
title_full Silk fibroin as an additive for cell-free protein synthesis
title_fullStr Silk fibroin as an additive for cell-free protein synthesis
title_full_unstemmed Silk fibroin as an additive for cell-free protein synthesis
title_short Silk fibroin as an additive for cell-free protein synthesis
title_sort silk fibroin as an additive for cell-free protein synthesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320238/
https://www.ncbi.nlm.nih.gov/pubmed/32637668
http://dx.doi.org/10.1016/j.synbio.2020.06.004
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