Gnaiger 1998 BTK-HRR: Difference between revisions

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{{Publication
{{Publication
|title=Gnaiger E, Kuznetsov AV, Lassnig B, Fuchs A, Reck M, Renner K, Stadlmann S, Rieger G, Margreiter R (1998) High-resolution respirometry. Optimum permeabilization of the cell membrane by digitonin. In BioThermoKinetics in the Post Genomic Era (Larsson C, PΓ₯hlman I-L, Gustafsson L, eds) Chalmers Reproservice, GΓΆteborg: 89-95.
|title=Gnaiger E, Kuznetsov AV, Lassnig B, Fuchs A, Reck M, Renner K, Stadlmann S, Rieger G, Margreiter R (1998) High-resolution respirometry. Optimum permeabilization of the cell membrane by digitonin. In BioThermoKinetics in the Post Genomic Era (Larsson C, Pahlman I-L, Gustafsson L, eds) Chalmers Reproservice, GΓΆteborg:89-95.
|authors=Gnaiger E, Kuznetsov AV, Lassnig B, Fuchs A, Reck M, Renner K, Stadlmann S, Rieger G, Margreiter R Β 
|info=[[Media:BTK_89-95_HRR.pdf| '''BTK 1998: 89-95 pdf'']]
|authors=Gnaiger Erich, Kuznetsov AV, Lassnig B, Fuchs A, Reck M, Renner K, Stadlmann S, Rieger G, Margreiter R
|year=1998
|year=1998
|mipnetlab=AT_Innsbruck_GnaigerE
|journal=Chalmers Reproservice
|abstract=Permeabilization of the cell membrane is becoming an established alternative to the isolation of mitochondria in bioenergetic studies of cultured cells and biopsy samples of muscle. Depending on cell type, 5 to 50 million cells are required for a respirometric measurement of endogenous and permeabilized-cell respiration [1,2], using conventional oxygen monitoring instruments. An order of magnitude less cells are required when using highresolution respirometry [3] (Tab. 1), which provides an up-to-date standard for general and clinical bioenergetics, including the diagnosis of mitochondrial defects, testing of drugs, oxidative stress and hypoxia-reoxygenation injury [4-6]. We provide an overview of (i) the specific features of high-resolution respirometry, (ii)
|abstract=Permeabilization of the cell membrane is becoming an established alternative to the isolation of mitochondria in bioenergetic studies of cultured cells and biopsy samples of muscle. Depending on cell type, 5 to 50 million cells are required for a respirometric measurement of endogenous and permeabilized-cell respiration [1,2], using conventional oxygen monitoring instruments. An order of magnitude less cells are required when using high-resolution respirometry [3] (Tab. 1), which provides an up-to-date standard for general and clinical bioenergetics, including the diagnosis of mitochondrial defects, testing of drugs, oxidative stress and hypoxia-reoxygenation injury [4-6]. We provide an overview of (i) the specific features of high-resolution respirometry, (ii) test experiments for instrumental evaluation, and (iii) digitonin titrations for determining optimum concentrations for cell membrane permeabilization in cultured cells.
test experiments for instrumental evaluation, and (iii) digitonin titrations for determining optimum concentrations for cell membrane permeabilization in cultured cells.
|mipnetlab=AT Innsbruck Gnaiger E, DE Regensburg Renner-Sattler K
|info=[http://www.oroboros.at/fileadmin/user_upload/Reprints/1998_Gnaiger_et_al_BTK_HRrespirometry.pdf BTK 1998: 89-95]
|discipline=Mitochondrial Physiology
}}
}}
{{Labeling
{{Labeling
|instruments=Oxygraph-2k, TIP2k, DatLab Software; Separate Application, Method
|area=Respiration, Instruments;methods
|organism=Human
|tissues=Endothelial;epithelial;mesothelial cell, HUVEC
|preparations=Intact cells, Permeabilized cells
|topics=Inhibitor, Oxygen kinetics, Substrate
|couplingstates=ROUTINE, OXPHOS
|pathways=S
|instruments=Oxygraph-2k, TIP2k
|discipline=Mitochondrial Physiology
|discipline=Mitochondrial Physiology
|organism=Human
|tissues=Endothelial; Epithelial; Mesothelial Cell
|preparations=Intact Cell; Cultured; Primary, Permeabilized Cell or Tissue; Homogenate
|topics=Respiration; OXPHOS; ETS Capacity, Coupling; Membrane Potential, Substrate; Glucose; TCA Cycle
}}
}}

Latest revision as of 04:26, 23 November 2021

Publications in the MiPMap
Gnaiger E, Kuznetsov AV, Lassnig B, Fuchs A, Reck M, Renner K, Stadlmann S, Rieger G, Margreiter R (1998) High-resolution respirometry. Optimum permeabilization of the cell membrane by digitonin. In BioThermoKinetics in the Post Genomic Era (Larsson C, Pahlman I-L, Gustafsson L, eds) Chalmers Reproservice, GΓΆteborg:89-95.

Β» 'BTK 1998: 89-95 pdf

Gnaiger Erich, Kuznetsov AV, Lassnig B, Fuchs A, Reck M, Renner K, Stadlmann S, Rieger G, Margreiter R (1998) Chalmers Reproservice

Abstract: Permeabilization of the cell membrane is becoming an established alternative to the isolation of mitochondria in bioenergetic studies of cultured cells and biopsy samples of muscle. Depending on cell type, 5 to 50 million cells are required for a respirometric measurement of endogenous and permeabilized-cell respiration [1,2], using conventional oxygen monitoring instruments. An order of magnitude less cells are required when using high-resolution respirometry [3] (Tab. 1), which provides an up-to-date standard for general and clinical bioenergetics, including the diagnosis of mitochondrial defects, testing of drugs, oxidative stress and hypoxia-reoxygenation injury [4-6]. We provide an overview of (i) the specific features of high-resolution respirometry, (ii) test experiments for instrumental evaluation, and (iii) digitonin titrations for determining optimum concentrations for cell membrane permeabilization in cultured cells.


β€’ O2k-Network Lab: AT Innsbruck Gnaiger E, DE Regensburg Renner-Sattler K


Labels: MiParea: Respiration, Instruments;methods 


Organism: Human  Tissue;cell: Endothelial;epithelial;mesothelial cell, HUVEC  Preparation: Intact cells, Permeabilized cells 

Regulation: Inhibitor, Oxygen kinetics, Substrate  Coupling state: ROUTINE, OXPHOS  Pathway:HRR: Oxygraph-2k, TIP2k 


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