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Measuring CPT-1-mediated respiration in permeabilized cells and isolated mitochondria

Carnitine palmitoyltransferase-1 (CPT-1) is a rate-controlling enzyme for long-chain fatty acid oxidation. This manuscript provides protocols for measuring CPT-1-mediated respiration in permeabilized, adherent cell monolayers and mitochondria freshly isolated from tissue, along with examples to asse...

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Detalles Bibliográficos
Autores principales: Yang, Krista, Doan, Mary T., Stiles, Linsey, Divakaruni, Ajit S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8348308/
https://www.ncbi.nlm.nih.gov/pubmed/34401773
http://dx.doi.org/10.1016/j.xpro.2021.100687
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author Yang, Krista
Doan, Mary T.
Stiles, Linsey
Divakaruni, Ajit S.
author_facet Yang, Krista
Doan, Mary T.
Stiles, Linsey
Divakaruni, Ajit S.
author_sort Yang, Krista
collection PubMed
description Carnitine palmitoyltransferase-1 (CPT-1) is a rate-controlling enzyme for long-chain fatty acid oxidation. This manuscript provides protocols for measuring CPT-1-mediated respiration in permeabilized, adherent cell monolayers and mitochondria freshly isolated from tissue, along with examples to assess the potency and specificity of interventions targeting CPT-1. Strengths of the approach include ease, speed, and breadth of analysis, whereas drawbacks include loss of physiological regulation in reductionist systems and indirect assessment of CPT-1 enzymatic activity. For complete details on the use and execution of this protocol, please refer to Divakaruni et al. (2018).
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spelling pubmed-83483082021-08-15 Measuring CPT-1-mediated respiration in permeabilized cells and isolated mitochondria Yang, Krista Doan, Mary T. Stiles, Linsey Divakaruni, Ajit S. STAR Protoc Protocol Carnitine palmitoyltransferase-1 (CPT-1) is a rate-controlling enzyme for long-chain fatty acid oxidation. This manuscript provides protocols for measuring CPT-1-mediated respiration in permeabilized, adherent cell monolayers and mitochondria freshly isolated from tissue, along with examples to assess the potency and specificity of interventions targeting CPT-1. Strengths of the approach include ease, speed, and breadth of analysis, whereas drawbacks include loss of physiological regulation in reductionist systems and indirect assessment of CPT-1 enzymatic activity. For complete details on the use and execution of this protocol, please refer to Divakaruni et al. (2018). Elsevier 2021-07-31 /pmc/articles/PMC8348308/ /pubmed/34401773 http://dx.doi.org/10.1016/j.xpro.2021.100687 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Yang, Krista
Doan, Mary T.
Stiles, Linsey
Divakaruni, Ajit S.
Measuring CPT-1-mediated respiration in permeabilized cells and isolated mitochondria
title Measuring CPT-1-mediated respiration in permeabilized cells and isolated mitochondria
title_full Measuring CPT-1-mediated respiration in permeabilized cells and isolated mitochondria
title_fullStr Measuring CPT-1-mediated respiration in permeabilized cells and isolated mitochondria
title_full_unstemmed Measuring CPT-1-mediated respiration in permeabilized cells and isolated mitochondria
title_short Measuring CPT-1-mediated respiration in permeabilized cells and isolated mitochondria
title_sort measuring cpt-1-mediated respiration in permeabilized cells and isolated mitochondria
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8348308/
https://www.ncbi.nlm.nih.gov/pubmed/34401773
http://dx.doi.org/10.1016/j.xpro.2021.100687
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