Literature DB >> 6234264

Homogeneity among mitochondria revealed by a constant proportion of their enzymes.

E Knecht, J Hernández-Yago, S Grisolía.   

Abstract

The homogeneity or heterogeneity at the enzyme level of mitochondria has not been directly demonstrated and is important for many studies. To clarify this point, carbamoyl phosphate synthase (ammonia), glutamate dehydrogenase and mitochondrial adenosine triphosphatase (F1) were located in rat liver by immunolabeling using protein A-gold. Measurements of the number of gold particles per square micron of cross sectional images of mitochondria permit to assess the relative molecular concentration of the three enzymes and, most interestingly, it presents the first evidence that different mitochondria in rat liver cells have the same relative proportion of the three enzymes. Since they have vastly different half-lives, bulk or unregulated autophagy as the main mechanism regulating the turnover of these enzymes seems unlikely.

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Year:  1984        PMID: 6234264     DOI: 10.1007/bf00495417

Source DB:  PubMed          Journal:  Histochemistry        ISSN: 0301-5564


  16 in total

1.  Crystallization and some properties of glutamate dehydrogenase from rat liver.

Authors:  H Arnold; K P Maier
Journal:  Biochim Biophys Acta       Date:  1971-11-19

2.  A major polypeptide component of rat liver mitochondria: carbamyl phosphate synthetase.

Authors:  S Clarke
Journal:  J Biol Chem       Date:  1976-02-25       Impact factor: 5.157

3.  Turnover of carbamyl-phosphate synthase, of other mitochondrial enzymes and of rat tissues. Effect of diet and of thyroidectomy.

Authors:  M Nicoletti; C Guerri; S Grisolia
Journal:  Eur J Biochem       Date:  1977-05-16

4.  Immunoferritin location of carbamoyl phosphate synthetase in rat liver.

Authors:  E Knecht; J Hernández; R Wallace; S Grisolía
Journal:  J Histochem Cytochem       Date:  1979-05       Impact factor: 2.479

5.  Ultrastructural localization of intracellular antigens by the use of protein A-gold complex.

Authors:  J Roth; M Bendayan; L Orci
Journal:  J Histochem Cytochem       Date:  1978-12       Impact factor: 2.479

Review 6.  Some recent developments in immunocytochemistry.

Authors:  F T Bosman
Journal:  Histochem J       Date:  1983-03

7.  Demonstration of an ATP-dependent, vanadate-sensitive endoprotease in the matrix of rat liver mitochondria.

Authors:  M Desautels; A L Goldberg
Journal:  J Biol Chem       Date:  1982-10-10       Impact factor: 5.157

8.  Fate of proteins synthesized in mitochondria of cultured mammalian cells revealed by electron microscope radioautography.

Authors:  E Knecht; J Hernández-Yago; A Martinez-Ramón; S Grisolía
Journal:  Exp Cell Res       Date:  1980-01       Impact factor: 3.905

9.  Carbamoyl phosphate synthetase I of human liver. Purification, some properties and immunological cross-reactivity with the rat liver enzyme.

Authors:  V Rubio; G Ramponi; S Grisolia
Journal:  Biochim Biophys Acta       Date:  1981-05-14

10.  Immunocytochemical localization of mitochondrial proteins in the rat hepatocyte.

Authors:  M Bendayan; G C Shore
Journal:  J Histochem Cytochem       Date:  1982-02       Impact factor: 2.479

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  3 in total

1.  microRNA-mediated differential expression of TRMU, GTPBP3 and MTO1 in cell models of mitochondrial-DNA diseases.

Authors:  Salvador Meseguer; Olga Boix; Carmen Navarro-González; Magda Villarroya; Rachid Boutoual; Sonia Emperador; Elena García-Arumí; Julio Montoya; M-Eugenia Armengod
Journal:  Sci Rep       Date:  2017-07-24       Impact factor: 4.379

2.  Defective Expression of the Mitochondrial-tRNA Modifying Enzyme GTPBP3 Triggers AMPK-Mediated Adaptive Responses Involving Complex I Assembly Factors, Uncoupling Protein 2, and the Mitochondrial Pyruvate Carrier.

Authors:  Ana Martínez-Zamora; Salvador Meseguer; Juan M Esteve; Magda Villarroya; Carmen Aguado; J Antonio Enríquez; Erwin Knecht; M-Eugenia Armengod
Journal:  PLoS One       Date:  2015-12-07       Impact factor: 3.240

3.  Defects in the mitochondrial-tRNA modification enzymes MTO1 and GTPBP3 promote different metabolic reprogramming through a HIF-PPARγ-UCP2-AMPK axis.

Authors:  Rachid Boutoual; Salvador Meseguer; Magda Villarroya; Elena Martín-Hernández; Mohammed Errami; Miguel A Martín; Marta Casado; M-Eugenia Armengod
Journal:  Sci Rep       Date:  2018-01-18       Impact factor: 4.379

  3 in total

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