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Protocol to Fabricate Engineered Illumination Devices for Optogenetic Control of Cellular Signaling Dynamics

Optogenetic modulation of protein interactions enables spatiotemporal control of cellular signaling dynamics in a variety of biological systems. However, light patterning by standard microscopes is limited by their complexity, sample throughput, and cost. To address the need for low-cost, user-frien...

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Detalles Bibliográficos
Autores principales: Repina, Nicole A., Johnson, Hunter J., McClave, Thomas, Kane, Ravi S., Schaffer, David V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757298/
https://www.ncbi.nlm.nih.gov/pubmed/33377035
http://dx.doi.org/10.1016/j.xpro.2020.100141
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author Repina, Nicole A.
Johnson, Hunter J.
McClave, Thomas
Kane, Ravi S.
Schaffer, David V.
author_facet Repina, Nicole A.
Johnson, Hunter J.
McClave, Thomas
Kane, Ravi S.
Schaffer, David V.
author_sort Repina, Nicole A.
collection PubMed
description Optogenetic modulation of protein interactions enables spatiotemporal control of cellular signaling dynamics in a variety of biological systems. However, light patterning by standard microscopes is limited by their complexity, sample throughput, and cost. To address the need for low-cost, user-friendly, and high-throughput photopatterning, we have engineered devices for light activation at variable amplitudes (LAVA). This protocol describes the assembly of LAVA devices, which enable spatial and temporal control of optogenetic stimulation and cellular signaling dynamics in multiwell cell culture plates. For complete details on the use and execution of this protocol, please refer to Repina et al. (2020).
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spelling pubmed-77572982020-12-28 Protocol to Fabricate Engineered Illumination Devices for Optogenetic Control of Cellular Signaling Dynamics Repina, Nicole A. Johnson, Hunter J. McClave, Thomas Kane, Ravi S. Schaffer, David V. STAR Protoc Protocol Optogenetic modulation of protein interactions enables spatiotemporal control of cellular signaling dynamics in a variety of biological systems. However, light patterning by standard microscopes is limited by their complexity, sample throughput, and cost. To address the need for low-cost, user-friendly, and high-throughput photopatterning, we have engineered devices for light activation at variable amplitudes (LAVA). This protocol describes the assembly of LAVA devices, which enable spatial and temporal control of optogenetic stimulation and cellular signaling dynamics in multiwell cell culture plates. For complete details on the use and execution of this protocol, please refer to Repina et al. (2020). Elsevier 2020-10-21 /pmc/articles/PMC7757298/ /pubmed/33377035 http://dx.doi.org/10.1016/j.xpro.2020.100141 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
Repina, Nicole A.
Johnson, Hunter J.
McClave, Thomas
Kane, Ravi S.
Schaffer, David V.
Protocol to Fabricate Engineered Illumination Devices for Optogenetic Control of Cellular Signaling Dynamics
title Protocol to Fabricate Engineered Illumination Devices for Optogenetic Control of Cellular Signaling Dynamics
title_full Protocol to Fabricate Engineered Illumination Devices for Optogenetic Control of Cellular Signaling Dynamics
title_fullStr Protocol to Fabricate Engineered Illumination Devices for Optogenetic Control of Cellular Signaling Dynamics
title_full_unstemmed Protocol to Fabricate Engineered Illumination Devices for Optogenetic Control of Cellular Signaling Dynamics
title_short Protocol to Fabricate Engineered Illumination Devices for Optogenetic Control of Cellular Signaling Dynamics
title_sort protocol to fabricate engineered illumination devices for optogenetic control of cellular signaling dynamics
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757298/
https://www.ncbi.nlm.nih.gov/pubmed/33377035
http://dx.doi.org/10.1016/j.xpro.2020.100141
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