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Difference between revisions of "Chinopoulos 2014 Methods Enzymol"

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|title=Chinopoulos C, Kiss G, Kawamata H, Starkov AA (2014) Measurement of ADP-ATP exchange in relation to mitochondrial transmembrane potential and oxygen consumption. Methods Enzymol 542:333-48.
|title=Chinopoulos C, Kiss G, Kawamata H, Starkov AA (2014) Measurement of ADP-ATP exchange in relation to mitochondrial transmembrane potential and oxygen consumption. Methods Enzymol 542:333-48.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/24862274 PMID: 24862274]»[[File:O2k-brief.png|36px|link=https://wiki.oroboros.at/images/1/1c/Chinopoulos_2014_Methods_Enzymol_O2k-brief.pdf|O2k-brief]]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/24862274 PMID: 24862274]»[[File:O2k-brief.png|36px|link=https://wiki.oroboros.at/images/1/1c/Chinopoulos_2014_Methods_Enzymol_O2k-brief.pdf|O2k-brief]]
|authors=Chinopoulos C, Kiss G, Kawamata H, Starkov AA
|authors=Chinopoulos Christos, Kiss Gergely, Kawamata Hibiki, Starkov Anatoly A
|year=2014
|year=2014
|journal=Methods Enzymol
|journal=Methods Enzymol
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|couplingstates=LEAK, OXPHOS
|couplingstates=LEAK, OXPHOS
|instruments=Oxygraph-2k, O2k-Fluorometer
|instruments=Oxygraph-2k, O2k-Fluorometer
|additional=Safranin, MgG
|additional=Safranin, MgG, O2k-brief, ATP
}}
}}

Revision as of 15:04, 14 October 2020

Publications in the MiPMap
Chinopoulos C, Kiss G, Kawamata H, Starkov AA (2014) Measurement of ADP-ATP exchange in relation to mitochondrial transmembrane potential and oxygen consumption. Methods Enzymol 542:333-48.

» PMID: 24862274»O2k-brief

Chinopoulos Christos, Kiss Gergely, Kawamata Hibiki, Starkov Anatoly A (2014) Methods Enzymol

Abstract: We have previously described a fluorometric method to measure ADP-ATP exchange rates in mitochondria of permeabilized cells, in which several enzymes that consume substantial amounts of ATP and other competing reactions interconverting adenine nucleotides are present. This method relies on recording changes in free extramitochondrial Mg(2+) with the Mg(2+)-sensitive fluorescent indicator Magnesium Green (MgGr)™, exploiting the differential affinity of ADP and ATP for Mg(2+). In particular, cells are permeabilized with digitonin in the presence of [Formula: see text] and Na3VO4, inhibiting all ATP- and ADP-utilizing reactions but mitochondrial exchange of ATP with ADP catalyzed by the adenine nucleotide translocase. The rate of ATP appearing in the medium upon the addition of ADP to energized mitochondria is then calculated from the rate of change in free extramitochondrial Mg(2+) using standard binding equations. Here, we describe a variant of this method involving an improved calibration step. This step minimizes errors that may be introduced during the conversion of the MgGr™ signal into free extramitochondrial [Mg(2+)] and ATP. Furthermore, we describe an approach for combining this methodology with the measurement of mitochondrial membrane potential and oxygen consumption in the same sample. The method described herein is useful for the study of malignant cells, which are known to thrive in hypoxic environments and to harbor mitochondria with profound functional alterations. Keywords: ADP–ATP exchange, Adenine nucleotide carrier, Adenine nucleotide translocase, Bioenergetics, Oxidative phosphorylation, Systems biology, Magnesium Green, High-resolution respirometry, Mitochondrial membrane potential, Safranin

O2k-Network Lab: HU Budapest Chinopoulos C


» O2k-Fluorometry protocol for Magnesium green


Methods Enzymol

  • Galluzzi L, Kroemer G (ed) (2014) Conceptual background and bioenergetic/mitochondrial aspects of oncometabolism. Methods Enzymol 542: 509 pp. »Link

O2k-Publications


Labels: MiParea: Respiration, Instruments;methods 


Organism: Human  Tissue;cell: HEK  Preparation: Permeabilized cells  Enzyme: Adenine nucleotide translocase 

Coupling state: LEAK, OXPHOS 

HRR: Oxygraph-2k, O2k-Fluorometer 

Safranin, MgG, O2k-brief, ATP