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Laser microirradiation as a tool to investigate the role of liquid-liquid phase separation in DNA damage repair

Here we describe a protocol for the generation of site-specific DNA damage, including double and single strand breaks, using the 405 nm laser of a confocal microscope in cells pre-sensitized with Hoechst. This is a simple approach, particularly useful to assess the involvement of proteins and the ro...

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Detalles Bibliográficos
Autores principales: Levone, Brunno Rocha, Lombardi, Silvia, Barabino, Silvia M.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819395/
https://www.ncbi.nlm.nih.gov/pubmed/35146448
http://dx.doi.org/10.1016/j.xpro.2022.101146
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author Levone, Brunno Rocha
Lombardi, Silvia
Barabino, Silvia M.L.
author_facet Levone, Brunno Rocha
Lombardi, Silvia
Barabino, Silvia M.L.
author_sort Levone, Brunno Rocha
collection PubMed
description Here we describe a protocol for the generation of site-specific DNA damage, including double and single strand breaks, using the 405 nm laser of a confocal microscope in cells pre-sensitized with Hoechst. This is a simple approach, particularly useful to assess the involvement of proteins and the roles of liquid-liquid phase separation in DNA damage repair. Examples of transfection protocol, drug concentrations, and microscopy are provided, although optimization may be needed for specific experimental setups and cell lines used. For complete details on the use and execution of this protocol, please refer to Levone et al. (2021).
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spelling pubmed-88193952022-02-09 Laser microirradiation as a tool to investigate the role of liquid-liquid phase separation in DNA damage repair Levone, Brunno Rocha Lombardi, Silvia Barabino, Silvia M.L. STAR Protoc Protocol Here we describe a protocol for the generation of site-specific DNA damage, including double and single strand breaks, using the 405 nm laser of a confocal microscope in cells pre-sensitized with Hoechst. This is a simple approach, particularly useful to assess the involvement of proteins and the roles of liquid-liquid phase separation in DNA damage repair. Examples of transfection protocol, drug concentrations, and microscopy are provided, although optimization may be needed for specific experimental setups and cell lines used. For complete details on the use and execution of this protocol, please refer to Levone et al. (2021). Elsevier 2022-02-03 /pmc/articles/PMC8819395/ /pubmed/35146448 http://dx.doi.org/10.1016/j.xpro.2022.101146 Text en © 2022 The Author(s) https://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
Levone, Brunno Rocha
Lombardi, Silvia
Barabino, Silvia M.L.
Laser microirradiation as a tool to investigate the role of liquid-liquid phase separation in DNA damage repair
title Laser microirradiation as a tool to investigate the role of liquid-liquid phase separation in DNA damage repair
title_full Laser microirradiation as a tool to investigate the role of liquid-liquid phase separation in DNA damage repair
title_fullStr Laser microirradiation as a tool to investigate the role of liquid-liquid phase separation in DNA damage repair
title_full_unstemmed Laser microirradiation as a tool to investigate the role of liquid-liquid phase separation in DNA damage repair
title_short Laser microirradiation as a tool to investigate the role of liquid-liquid phase separation in DNA damage repair
title_sort laser microirradiation as a tool to investigate the role of liquid-liquid phase separation in dna damage repair
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819395/
https://www.ncbi.nlm.nih.gov/pubmed/35146448
http://dx.doi.org/10.1016/j.xpro.2022.101146
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