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In situ measurements of mitochondrial matrix enzyme activities using plasma and mitochondrial membrane permeabilization agents

Divakaruni, Ajit S., Andreyev, Alexander Y., Rogers, George W., Murphy, Anne N.·2018·Analytical Biochemistry
DOI 10.1016/j.ab.2017.09.019PMC PMC5882612
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  3. Rogers, 2011, High throughput microplate respiratory measurements using minimal quantities of isolated mitochondria, PLoS One, 6, e21746, 10.1371/journal.pone.0021746 · DOI
  4. Divakaruni, 2014, Measuring mitochondrial function in permeabilized cells using the Seahorse XF Analyzer or a Clark-type oxygen electrode, Curr. Protoc. Toxicol., 60, 25.2.1, 10.1002/0471140856.tx2502s60 · DOI
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  10. Divakaruni, 2017, Inhibition of the mitochondrial pyruvate carrier protects from excitotoxic neuronal death, J. Cell Biol., 216, 1091, 10.1083/jcb.201612067 · DOI
  11. Matlib, 1977, Measurement of matrix enzyme activity in isolated mitochondria made permeable with toluene, Archives Biochem. Biophys., 178, 396, 10.1016/0003-9861(77)90209-0 · DOI
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  13. Midgley, 1987, Effects of Ca2+ and Mg2+ on the activity of pyruvate dehydrogenase phosphate phosphatase within toluene-permeabilized mitochondria, Biochem. J., 241, 371, 10.1042/bj2410371 · DOI
  14. Rutter, 1988, Regulation of NAD+-linked isocitrate dehydrogenase and 2-oxoglutarate dehydrogenase by Ca2+ ions within toluene-permeabilized rat heart mitochondria. Interactions with regulation by adenine nucleotides and NADH/NAD+ ratios, Biochem. J., 252, 181, 10.1042/bj2520181 · DOI
  15. Moe, 2010, Phospholipid hydrolysis caused by Clostridium perfringens α-toxin facilitates the targeting of perfringolysin O to membrane bilayers, Biochemistry, 49, 9498, 10.1021/bi1013886 · DOI
  16. Johnson, 2012, Modifications in perfringolysin O domain 4 alter the cholesterol concentration threshold required for binding, Biochemistry, 51, 3373, 10.1021/bi3003132 · DOI
  17. Gostimskaya, 2003, In situ assay of the intramitochondrial enzymes: use of alamethicin for permeabilization of mitochondria, Anal. Biochem., 313, 46, 10.1016/S0003-2697(02)00534-1 · DOI
  18. Pfeiffer, 1995, The peptide mastoparan is a potent facilitator of the mitochondrial permeability transition, J. Biol. Chem., 270, 4923, 10.1074/jbc.270.9.4923 · DOI
  19. Pieta, 2012, Direct visualization of the alamethicin pore formed in a planar phospholipid matrix, Proc. Natl. Acad. Sci. U. S. A., 109, 21223, 10.1073/pnas.1201559110 · DOI
  20. Andreyev, 1998, Cytochrome c release from brain mitochondria is independent of the mitochondrial permeability transition, FEBS Lett., 439, 373, 10.1016/S0014-5793(98)01394-5 · DOI
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  22. Robinson, 2007, Novel mechanism of inhibition of rat kidney-type glutaminase by bis-2-(5-phenylacetamido-1,2,4-thiadiazol-2-yl)ethyl sulfide (BPTES), Biochem. J., 406, 407, 10.1042/BJ20070039 · DOI
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Cited by

Sorted by citations

Metadata

Authors
Divakaruni, A. S., Andreyev, A. Y., Rogers, G. W., & Murphy, A. N.
ORCID
Venue
Analytical Biochemistry
Publisher
Elsevier BV
Published
2018-07
Volume
552
Pages
60-65
ISSN
0003-2697
DOI
10.1016/j.ab.2017.09.019
PMC
PMC5882612
Cited by
18
References
2
Language
en
Licence
Funders
  • US National Institutes of Health (R01NS087611)
  • Agilent Technologies

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