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Microfluidic encapsulation of Xenopus laevis cell-free extracts using hydrogel photolithography

Cell-free extract derived from the eggs of the African clawed frog Xenopus laevis is a well-established model system that has been used historically in bulk aliquots. Here, we describe a microfluidic approach for isolating discrete, biologically relevant volumes of cell-free extract, with more expan...

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Detalles Bibliográficos
Autores principales: Geisterfer, Zachary M., Oakey, John, Gatlin, Jesse C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757658/
https://www.ncbi.nlm.nih.gov/pubmed/33377113
http://dx.doi.org/10.1016/j.xpro.2020.100221
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author Geisterfer, Zachary M.
Oakey, John
Gatlin, Jesse C.
author_facet Geisterfer, Zachary M.
Oakey, John
Gatlin, Jesse C.
author_sort Geisterfer, Zachary M.
collection PubMed
description Cell-free extract derived from the eggs of the African clawed frog Xenopus laevis is a well-established model system that has been used historically in bulk aliquots. Here, we describe a microfluidic approach for isolating discrete, biologically relevant volumes of cell-free extract, with more expansive and precise control of extract shape compared with extract-oil emulsions. This approach is useful for investigating the mechanics of intracellular processes affected by cell geometry or cytoplasmic volume, including organelle scaling and positioning mechanisms. For complete details on the use and execution of this protocol, please refer to Geisterfer et al. (2020).
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spelling pubmed-77576582020-12-28 Microfluidic encapsulation of Xenopus laevis cell-free extracts using hydrogel photolithography Geisterfer, Zachary M. Oakey, John Gatlin, Jesse C. STAR Protoc Protocol Cell-free extract derived from the eggs of the African clawed frog Xenopus laevis is a well-established model system that has been used historically in bulk aliquots. Here, we describe a microfluidic approach for isolating discrete, biologically relevant volumes of cell-free extract, with more expansive and precise control of extract shape compared with extract-oil emulsions. This approach is useful for investigating the mechanics of intracellular processes affected by cell geometry or cytoplasmic volume, including organelle scaling and positioning mechanisms. For complete details on the use and execution of this protocol, please refer to Geisterfer et al. (2020). Elsevier 2020-12-11 /pmc/articles/PMC7757658/ /pubmed/33377113 http://dx.doi.org/10.1016/j.xpro.2020.100221 Text en © 2020 The Authors 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 Protocol
Geisterfer, Zachary M.
Oakey, John
Gatlin, Jesse C.
Microfluidic encapsulation of Xenopus laevis cell-free extracts using hydrogel photolithography
title Microfluidic encapsulation of Xenopus laevis cell-free extracts using hydrogel photolithography
title_full Microfluidic encapsulation of Xenopus laevis cell-free extracts using hydrogel photolithography
title_fullStr Microfluidic encapsulation of Xenopus laevis cell-free extracts using hydrogel photolithography
title_full_unstemmed Microfluidic encapsulation of Xenopus laevis cell-free extracts using hydrogel photolithography
title_short Microfluidic encapsulation of Xenopus laevis cell-free extracts using hydrogel photolithography
title_sort microfluidic encapsulation of xenopus laevis cell-free extracts using hydrogel photolithography
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757658/
https://www.ncbi.nlm.nih.gov/pubmed/33377113
http://dx.doi.org/10.1016/j.xpro.2020.100221
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