Saks 2001 Biochem J: Difference between revisions

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{{Publication
{{Publication
|title=Saks VA, Kaambre T, Sikk P, Eimre M, Orlova E, Paju K, Piirsoo A, Appaix F, Kay L, Regitz-Zagrosek V, Fleck E, Seppet E (2001) Intracellular energetic units in red muscle cells. Biochem J 356:643-57.
|title=Saks VA, Kaambre T, Sikk P, Eimre M, Orlova E, Paju K, Piirsoo A, Appaix F, Kay L, Regitz-Zagrosek V, Fleck E, Seppet E (2001) Intracellular energetic units in red muscle cells. Biochem J 356:643-57.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/11368796 PMID: 11368796]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/11368796 PMID: 11368796 Open Access]
|authors=Saks VA, Kaambre T, Sikk P, Eimre M, Orlova E, Paju K, Piirsoo A, Appaix F, Kay L, Regitz-Zagrosek V, Fleck E, Seppet E
|authors=Saks VA, Kaambre T, Sikk P, Eimre M, Orlova E, Paju K, Piirsoo A, Appaix F, Kay L, Regitz-Zagrosek V, Fleck E, Seppet E
|year=2001
|year=2001
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organization of muscle-cell energy metabolism.
organization of muscle-cell energy metabolism.
|keywords=ADP, ATPases, Compartmentation, Mitochondria, Myocytes
|keywords=ADP, ATPases, Compartmentation, Mitochondria, Myocytes
|mipnetlab=EE_Tartu_Seppet EK, EE_Tallinn_Saks VA, FR_Grenoble_Saks VA, EE Tallinn Kaambre T
|mipnetlab=EE Tartu Seppet EK, EE Tallinn Saks VA, FR Grenoble Saks VA, EE Tallinn Kaambre T
}}
}}
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|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
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Revision as of 16:03, 24 March 2015

Publications in the MiPMap
Saks VA, Kaambre T, Sikk P, Eimre M, Orlova E, Paju K, Piirsoo A, Appaix F, Kay L, Regitz-Zagrosek V, Fleck E, Seppet E (2001) Intracellular energetic units in red muscle cells. Biochem J 356:643-57.

ยป PMID: 11368796 Open Access

Saks VA, Kaambre T, Sikk P, Eimre M, Orlova E, Paju K, Piirsoo A, Appaix F, Kay L, Regitz-Zagrosek V, Fleck E, Seppet E (2001) Biochem J

Abstract: The kinetics of regulation of mitochondrial respiration by endogenous and exogenous ADP in muscle cells in situ was studied in skinned cardiac and skeletal muscle fibres. Endogenous ADP production was initiated by addition of MgATP; under these conditions the respiration rate and ADP concentration in the medium were dependent on the calcium concentration, and 70ยฑ80% of maximal rate of respiration was achieved at ADP concentration below 20 ยตM in the medium. In contrast, when exogenous ADP was added, maximal respiration rate was observed only at millimolar concentrations. An exogenous ADPconsuming system consisting of pyruvate kinase (PK; 20ยฑ 40 units}ml) and phosphoenolpyruvate (PEP; 5 mM), totally suppressed respiration activated by exogenous ADP, but the respiration maintained by endogenous ADP was not suppressed by more than 20ยฑ40%. Creatine (20 mM) further activated respiration in the presence of ATP and PKPEP. Short treatment with trypsin (50ยฑ500 nM for 5 min) decreased the apparent Km for exogenous ADP from 300ยฑ350 ยตM to 50ยฑ60 ยตM, increased inhibition of respiration by PKPEP system up to 70ยฑ80%,with no changes in MgATPase activity and maximal respiration rates. Electron-microscopic observations showed detachment of mitochondria and disordering of the regular structure of the sarcomere after trypsin treatment. Two-dimensional electrophoresis revealed a group of at least seven low-molecular-mass proteins in cardiac skinned fibres which were very sensitive to trypsin and not present in glycolytic fibres, which have low apparentKm for exogenous ADP. It is concluded that, in oxidative muscle cells, mitochondria are incorporated into functional complexes (`intracellular energetic units') with adjacent ADP producing systems in myofibrils and in sarcoplasmic reticulum, probably due to specific interaction with cytoskeletal elements responsible for mitochondrial distribution in the cell. It is suggested that these complexes represent the basic pattern of organization of muscle-cell energy metabolism. โ€ข Keywords: ADP, ATPases, Compartmentation, Mitochondria, Myocytes

โ€ข O2k-Network Lab: EE Tartu Seppet EK, EE Tallinn Saks VA, FR Grenoble Saks VA, EE Tallinn Kaambre T


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Tissue;cell: Heart, Skeletal muscle  Preparation: Permeabilized tissue, Isolated mitochondria 



HRR: Oxygraph-2k 


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