Figueira 2012 Methods Mol Biol: Difference between revisions
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{{Publication | {{Publication | ||
|title=Figueira TR, Melo DR, Vercesi AE, Castilho RF (2012) Safranine as a fluorescent probe for the evaluation of mitochondrial membrane potential in isolated organelles and permeabilized cells | |title=Figueira TR, Melo DR, Vercesi AE, Castilho RF (2012) Safranine as a fluorescent probe for the evaluation of mitochondrial membrane potential in isolated organelles and permeabilized cells. Methods Mol Biol 810:103-17. | ||
|info=[http://www.ncbi.nlm.nih.gov/pubmed/22057563 PMID:22057563] | |||
|authors=Figueira TR, Melo DR, Vercesi AE, Castilho RF | |authors=Figueira TR, Melo DR, Vercesi AE, Castilho RF | ||
|year=2012 | |year=2012 | ||
|journal=Methods Mol Biol | |journal=Methods Mol Biol | ||
|abstract=The mitochondrial electrical membrane potential (delta Psi) is the main component of the proton motive force (delta p) generated across the inner mitochondrial membrane during electron flow through the respiratory chain. Among the techniques available to assess delta Psi, methods that rely on the spectrophotofluorometric responses of dyes are widely employed for whole suspensions of isolated mitochondria or permeabilized cells. Safranine is one of the dyes currently used most often for this purpose. Safranine is a lipophilic cationic dye that undergoes optical shifts upon its potential-dependent distribution between the external medium and the intramitochondrial compartment and on its stacking to inner mitochondrial membrane anionic sites. The association between the optical changes of safranine and the membrane potential allows unknown delta Psi values to be estimated from an equation describing their relationship. Here, we describe the use of safranine as a fluorescent indicator of delta Psi in isolated mitochondria and digitonin-permeabilized cells. We present suitable conditions to employ safranine as a delta Psi indicator. | |abstract=The mitochondrial electrical membrane potential (delta Psi) is the main component of the proton motive force (delta ''p'') generated across the inner mitochondrial membrane during electron flow through the respiratory chain. Among the techniques available to assess delta Psi, methods that rely on the spectrophotofluorometric responses of dyes are widely employed for whole suspensions of isolated mitochondria or permeabilized cells. Safranine is one of the dyes currently used most often for this purpose. Safranine is a lipophilic cationic dye that undergoes optical shifts upon its potential-dependent distribution between the external medium and the intramitochondrial compartment and on its stacking to inner mitochondrial membrane anionic sites. The association between the optical changes of safranine and the membrane potential allows unknown delta Psi values to be estimated from an equation describing their relationship. Here, we describe the use of safranine as a fluorescent indicator of delta Psi in isolated mitochondria and digitonin-permeabilized cells. We present suitable conditions to employ safranine as a delta Psi indicator. | ||
|mipnetlab=BR Campinas Vercesi AE | |mipnetlab=BR Campinas Vercesi AE | ||
}} | }} | ||
== Cited by == | |||
{{Template:Cited by Komlodi 2021 MitoFit Tissue normoxia}} | |||
{{Template:Cited by Komlodi 2022 MitoFit pmF}} | |||
{{Labeling | {{Labeling | ||
| | |area=Instruments;methods | ||
|organism=Rat | |organism=Rat | ||
|tissues=Liver | |tissues=Liver, Other cell lines | ||
|preparations=Permeabilized cells, Isolated | |preparations=Permeabilized cells, Isolated mitochondria | ||
|topics=mt-Membrane potential | |topics=ADP, mt-Membrane potential, Uncoupler | ||
|instruments=O2k-Fluorometer, Theory | |||
|additional=MitoFit 2021 Tissue normoxia, MitoFit 2022 pmF | |||
}} | }} | ||
relationship between safranin fluorescence and mitochondrial membrane potential is discussed | The relationship between safranin fluorescence and mitochondrial membrane potential is discussed. |
Latest revision as of 00:33, 18 February 2022
Figueira TR, Melo DR, Vercesi AE, Castilho RF (2012) Safranine as a fluorescent probe for the evaluation of mitochondrial membrane potential in isolated organelles and permeabilized cells. Methods Mol Biol 810:103-17. |
Figueira TR, Melo DR, Vercesi AE, Castilho RF (2012) Methods Mol Biol
Abstract: The mitochondrial electrical membrane potential (delta Psi) is the main component of the proton motive force (delta p) generated across the inner mitochondrial membrane during electron flow through the respiratory chain. Among the techniques available to assess delta Psi, methods that rely on the spectrophotofluorometric responses of dyes are widely employed for whole suspensions of isolated mitochondria or permeabilized cells. Safranine is one of the dyes currently used most often for this purpose. Safranine is a lipophilic cationic dye that undergoes optical shifts upon its potential-dependent distribution between the external medium and the intramitochondrial compartment and on its stacking to inner mitochondrial membrane anionic sites. The association between the optical changes of safranine and the membrane potential allows unknown delta Psi values to be estimated from an equation describing their relationship. Here, we describe the use of safranine as a fluorescent indicator of delta Psi in isolated mitochondria and digitonin-permeabilized cells. We present suitable conditions to employ safranine as a delta Psi indicator.
โข O2k-Network Lab: BR Campinas Vercesi AE
Cited by
- Komlodi et al (2022) Hydrogen peroxide production, mitochondrial membrane potential and the coenzyme Q redox state measured at tissue normoxia and experimental hyperoxia in heart mitochondria. MitoFit Preprints 2021 (in prep)
- Komlรณdi et al (2022) The protonmotive force - not merely membrane potential. MitoFit Preprints 2022 (in prep)
- Komlodi et al (2022) Hydrogen peroxide production, mitochondrial membrane potential and the coenzyme Q redox state measured at tissue normoxia and experimental hyperoxia in heart mitochondria. MitoFit Preprints 2021 (in prep)
Labels: MiParea: Instruments;methods
Organism: Rat
Tissue;cell: Liver, Other cell lines
Preparation: Permeabilized cells, Isolated mitochondria
Regulation: ADP, mt-Membrane potential, Uncoupler
HRR: O2k-Fluorometer, Theory
MitoFit 2021 Tissue normoxia, MitoFit 2022 pmF
The relationship between safranin fluorescence and mitochondrial membrane potential is discussed.