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FLAMBE: A kinetic fluorescence polarization assay to study activation of monomeric BAX

BAX activation techniques are crucial to studying the intrinsic pathway of apoptosis— thousands of pro-apoptotic signals converge on BAX activation. Current methodologies are predominantly limited to membrane permeabilization studies, which assess endpoint functionality of oligomeric BAX, but overlo...

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Detalles Bibliográficos
Autores principales: Mohammed, Jarvier N., Gelles, Jesse D., Chipuk, Jerry Edward
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933840/
https://www.ncbi.nlm.nih.gov/pubmed/35313708
http://dx.doi.org/10.1016/j.xpro.2022.101252
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author Mohammed, Jarvier N.
Gelles, Jesse D.
Chipuk, Jerry Edward
author_facet Mohammed, Jarvier N.
Gelles, Jesse D.
Chipuk, Jerry Edward
author_sort Mohammed, Jarvier N.
collection PubMed
description BAX activation techniques are crucial to studying the intrinsic pathway of apoptosis— thousands of pro-apoptotic signals converge on BAX activation. Current methodologies are predominantly limited to membrane permeabilization studies, which assess endpoint functionality of oligomeric BAX, but overlook early activation steps of cytosolic BAX. Here we detail FLAMBE: a fluorescence polarization ligand assay for monitoring BAX early-activation in solution. We also describe a dual-metric parameterization strategy for distillation of kinetic data and comparative analyses when studying candidate ligands. For complete details on the use and execution of this protocol, please refer to Gelles et al. (2022).
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spelling pubmed-89338402022-03-20 FLAMBE: A kinetic fluorescence polarization assay to study activation of monomeric BAX Mohammed, Jarvier N. Gelles, Jesse D. Chipuk, Jerry Edward STAR Protoc Protocol BAX activation techniques are crucial to studying the intrinsic pathway of apoptosis— thousands of pro-apoptotic signals converge on BAX activation. Current methodologies are predominantly limited to membrane permeabilization studies, which assess endpoint functionality of oligomeric BAX, but overlook early activation steps of cytosolic BAX. Here we detail FLAMBE: a fluorescence polarization ligand assay for monitoring BAX early-activation in solution. We also describe a dual-metric parameterization strategy for distillation of kinetic data and comparative analyses when studying candidate ligands. For complete details on the use and execution of this protocol, please refer to Gelles et al. (2022). Elsevier 2022-03-18 /pmc/articles/PMC8933840/ /pubmed/35313708 http://dx.doi.org/10.1016/j.xpro.2022.101252 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
Mohammed, Jarvier N.
Gelles, Jesse D.
Chipuk, Jerry Edward
FLAMBE: A kinetic fluorescence polarization assay to study activation of monomeric BAX
title FLAMBE: A kinetic fluorescence polarization assay to study activation of monomeric BAX
title_full FLAMBE: A kinetic fluorescence polarization assay to study activation of monomeric BAX
title_fullStr FLAMBE: A kinetic fluorescence polarization assay to study activation of monomeric BAX
title_full_unstemmed FLAMBE: A kinetic fluorescence polarization assay to study activation of monomeric BAX
title_short FLAMBE: A kinetic fluorescence polarization assay to study activation of monomeric BAX
title_sort flambe: a kinetic fluorescence polarization assay to study activation of monomeric bax
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933840/
https://www.ncbi.nlm.nih.gov/pubmed/35313708
http://dx.doi.org/10.1016/j.xpro.2022.101252
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